Skip to content

Advertisement

You're viewing the new version of our site. Please leave us feedback.

Learn more

BMC Genetics

Open Access

Mechanisms of amino acid-mediated lifespan extension in Caenorhabditis elegans

  • Clare Edwards1,
  • John Canfield1,
  • Neil Copes1,
  • Andres Brito1,
  • Muhammad Rehan1,
  • David Lipps1,
  • Jessica Brunquell1,
  • Sandy D Westerheide1 and
  • Patrick C Bradshaw1Email author
BMC Genetics201516:8

https://doi.org/10.1186/s12863-015-0167-2

Received: 24 December 2014

Accepted: 16 January 2015

Published: 3 February 2015

Abstract

Background

Little is known about the role of amino acids in cellular signaling pathways, especially as it pertains to pathways that regulate the rate of aging. However, it has been shown that methionine or tryptophan restriction extends lifespan in higher eukaryotes and increased proline or tryptophan levels increase longevity in C. elegans. In addition, leucine strongly activates the TOR signaling pathway, which when inhibited increases lifespan.

Results

Therefore each of the 20 proteogenic amino acids was individually supplemented to C. elegans and the effects on lifespan were determined. All amino acids except phenylalanine and aspartate extended lifespan at least to a small extent at one or more of the 3 concentrations tested with serine and proline showing the largest effects. 11 of the amino acids were less potent at higher doses, while 5 even decreased lifespan. Serine, proline, or histidine-mediated lifespan extension was greatly inhibited in eat-2 worms, a model of dietary restriction, in daf-16/FOXO, sir-2.1, rsks-1 (ribosomal S6 kinase), gcn-2, and aak-2 (AMPK) longevity pathway mutants, and in bec-1 autophagy-defective knockdown worms. 8 of 10 longevity-promoting amino acids tested activated a SKN-1/Nrf2 reporter strain, while serine and histidine were the only amino acids from those to activate a hypoxia-inducible factor (HIF-1) reporter strain. Thermotolerance was increased by proline or tryptophan supplementation, while tryptophan-mediated lifespan extension was independent of DAF-16/FOXO and SKN-1/Nrf2 signaling, but tryptophan and several related pyridine-containing compounds induced the mitochondrial unfolded protein response and an ER stress response. High glucose levels or mutations affecting electron transport chain (ETC) function inhibited amino acid-mediated lifespan extension suggesting that metabolism plays an important role. Providing many other cellular metabolites to C. elegans also increased longevity suggesting that anaplerosis of tricarboxylic acid (TCA) cycle substrates likely plays a role in lifespan extension.

Conclusions

Supplementation of C. elegans with 18 of the 20 individual amino acids extended lifespan, but lifespan often decreased with increasing concentration suggesting hormesis. Lifespan extension appears to be caused by altered mitochondrial TCA cycle metabolism and respiratory substrate utilization resulting in the activation of the DAF-16/FOXO and SKN-1/Nrf2 stress response pathways.

Keywords

Amino acidsLifespanAging C. elegans SerineProlineHistidineTryptophanMitochondrial

Background

In C. elegans nematodes free amino acid concentrations change with age [1] and are altered in long-lived worms [2]. In humans, altered plasma amino acid concentrations are biomarkers of several diseases [3] such as type 2 diabetes [4]. Calorie restriction has long been known to delay aging [5] and protein restriction may be responsible for around half of this effect [6]. Methionine [7,8] or tryptophan [9,10] restriction partially mimics protein restriction to extend lifespan and delay aging-related disease in rodents. But the role that other amino acids play in longevity and disease has been harder to elucidate. In this regard, experiments with yeast, worms, and fruit flies are increasingly being used to address this issue.

Using the yeast Saccharomyces cerevisiae, it was first discovered that supplementation with the branched chain amino acids (leucine, isoleucine, or valine) or threonine extended chronological lifespan by downregulating the general amino acid control (GAAC) pathway [11]. Others found that glutamate supplementation extended chronological lifespan [12]. Consistent with the ability of glutamate to extend lifespan, deletion of genes involved in converting glutamate to gamma-aminobutyric acid (GABA) increased replicative lifespan [13] and led to increased conversion of glutamate to alpha-ketoglutarate and other TCA cycle intermediates, which may be involved in lifespan extension by maintaining mitochondrial respiratory function. Others using different conditions found that supplementation with serine, threonine, or valine decreased chronological lifespan [14] while limitation of asparagine [15], methionine, aspartate, or glutamate [12] extended lifespan. Further research using yeast deletion strains of differing lifespans found that intracellular levels of many amino acids positively correlated with lifespan [16].

In Drosophila, dietary restriction (DR) or protein restriction [17] extends lifespan and supplementing methionine in combination with one or more of the essential amino acids decreased the lifespan back to the fully fed level [18]. Interestingly, adding methionine by itself to DR flies increased protein translation [19] and fecundity [18] without decreasing lifespan, uncoupling these events. Increased levels of amino acids, especially leucine [20,21], activate the TOR kinase, which leads to an increased rate of translation. Inhibition of the TOR kinase with rapamycin [22] or expressing a dominant negative p70-S6 kinase, a kinase downstream of TOR, extended organismal longevity [23]. Metabolism of sulfur containing amino acids was shown to be essential for DR-mediated longevity in Drosophila [19], but supplementation of cysteine or methionine failed to extend lifespan in fully fed Drosophila [24,25]. However, supplementing casein and methionine together led to lifespan extension [24].

In C. elegans, proline supplementation extended lifespan that relied upon its catabolism and a transient increase in reactive oxygen species (ROS) production from the mitochondrial electron transport chain [26]. Increased tryptophan levels also increased longevity in C. elegans as knockdown of an enzyme that catabolizes tryptophan increased lifespan [27]. Unexpectedly, knockdown of an aromatic amino acid transporter also extended lifespan [28], suggesting that decreased tryptophan or other aromatic amino acid levels may also boost longevity. Others found that decreased tyrosine degradation led to increased longevity, but surprisingly supplementation of tyrosine to the culture medium did not extend lifespan [29]. The majority of amino acid pool sizes are upregulated in long-lived worms [2]. In daf-2 insulin-receptor deficient worms, for example, the levels of 8 of the 12 measured amino acids were increased, including the 3 branched chain amino acids. The branched chain amino acids are of special interest for longevity research, since their levels decreased to wild-type levels in the normal-lived daf-2/daf-16 double mutants [2].

Feeding mice a diet high in branched chain amino acids led to increased mitochondrial biogenesis in muscle, decreased ROS production, and increased average lifespan of males [30]. However, branched chain amino acid levels declined in long-lived metformin-treated worms [31], and increased plasma levels of branched chain amino acids are correlated with the development of insulin resistance and type 2 diabetes in humans [32]. Furthermore, studies correlating high levels of free amino acids with longevity must be interpreted with caution as a decreased rate of translation is frequently associated with or even required for longevity and the increased amino acid pools may just be a result of that decreased rate of protein synthesis [33,34].

Due to the incomplete knowledge of the effects of amino acids on longevity as well as the widespread use of amino acid and protein supplementation in the human diet we determined the effects of individual amino acid supplementation on C. elegans lifespan. We found that the vast majority of amino acids extended lifespan and further determined many of the signaling pathways required. We then tested the ability of several amino acids or tryptophan catabolites to induce a heat shock response, the ER stress response, or the mitochondrial unfolded protein response, which frequently accompany lifespan extension. The amino acids that extended lifespan to the greatest extent were then tested for effects on stress resistance and proteotoxicity.

Results

The effects of individual L-amino acids on the lifespan of C. elegans

We determined the effects of individually supplementing the 19 L-amino acids or glycine on the lifespan of C. elegans at 1 mM (Figure 1A), 5 mM (Figure 1B), and 10 mM (Figure 1C) concentrations. The percent change of mean lifespan compared to that of untreated controls performed at the same time is also shown as a table (Additional file 1: Table S1). C. elegans worms were grown in liquid S medium with heat-killed E. coli as food. Heat killing prevented or at least greatly reduced bacterial catabolism of the added amino acid. Unlike nematode growth medium (NGM) which is standardly used, the S medium contains no peptone, so the bacterial food source and the supplemented amino acid are the only sources of dietary amino acids.
Figure 1

Individual supplementation of most amino acids extends mean lifespan in C. elegans . Mean lifespan of C. elegans supplemented with a (A) 1 mM, (B) 5 mM, or (C) 10 mM concentration of each of the 20 amino acids (* log rank p < 0.05 vs. control).

The worms feeding on heat-killed bacteria had a mean lifespan of 17.2 +/− 0.3 days. At a 1 mM concentration, the amino acids that extended lifespan to the greatest extent (14-17%) were proline, leucine, glutamine, glutamate, and tryptophan. At a 5 mM concentration, the greatest lifespan extension was observed with proline, serine, cysteine, and glutamine (16-19%). At this concentration phenylalanine decreased lifespan (8%). Lastly, at a 10 mM concentration, the greatest increases in longevity were observed with serine, proline, arginine, and methionine addition (14-22%). Asparagine, aspartate, phenylalanine, glutamine, and glutamate decreased lifespan at this concentration (6-25%). 5 of the amino acids increased lifespan with increasing concentration from 1 to 10 mM (arginine, histidine, methionine, threonine, and serine), while 7 of the amino acids decreased lifespan with increasing concentration in this range (aspartate, glutamate, glycine, phenylalanine, tryptophan, tyrosine, and valine). 3 of the amino acids had the greatest lifespan extension at the 5 mM concentration (asparagine, cysteine, and glutamine), while the 5 mM concentration yielded the least lifespan extension for alanine. Example lifespan curves for serine, proline, histidine, and tryptophan at concentrations that yielded the greatest effects on mean lifespan are shown (Additional file 2: Figure S1).

The rate of amino acid uptake may limit the effect on lifespan

To determine if the rate of transport of amino acids into the worms may have limited their effects on lifespan, we administered the cell-permeable histidine analogs N-acetyl-histidine or histidine methylester, which get cleaved by intracellular enzymes to form histidine and monitored lifespan (Table 1). These compounds yielded greater lifespan extension than histidine at the 1 mM dose, suggesting that the rate of transport of the amino acids into the worms is likely limiting their effect on lifespan. The highest concentration of histidine methyl ester (10 mM) did not extend lifespan as expected for a hormetic dose response. If the same observation made for histidine holds for other amino acids, then the rate of amino acid absorption by the intestine may be an important factor controlling their ability to extend lifespan. The rate of transport of hydrophilic antioxidant compounds into C. elegans has also been shown to limit their effect on lifespan [35].
Table 1

The effects of D-amino acids and membrane-permeable L-histidine analogs on C. elegans N2 lifespan

Treatment

Concentration

% of untreated mean lifespan

p-value

# of worms

Replicates

D-alanine

1 mM

114

<0.001

219

2

5 mM

116

<0.001

273

2

10 mM

116

<0.001

240

2

D-aspartate

1 mM

107

0.024

233

2

5 mM

118

<0.001

269

2

10 mM

108

<0.001

228

2

D-glutamate

1 mM

114

<0.001

207

2

5 mM

118

<0.001

249

2

10 mM

97

0.165

232

2

D-serine

1 mM

100

0.600

209

2

5 mM

91

<0.001

198

2

10 mM

93

<0.001

220

2

D-proline

5 mM

101

0.734

113

2

N-acetyl-L-histidine

0.1 mM

103

0.383

142

2

1 mM

112

0.002

188

2

10 mM

110

0.008

196

2

L-histidine methyl ester

0.1 mM

108

<0.001

215

2

1 mM

109

<0.001

246

2

10 mM

104

0.11

193

2

The effects of D-amino acids on the lifespan of C. elegans

To determine if the effects on lifespan were specific for L-amino acids, we also determined if there were effects on longevity when supplementing the 4 D-amino acids found endogenously in C. elegans [36], D-alanine, D-serine, D-aspartate, or D-glutamate (Table 1 and Additional file 3: Figure S2) as well as D-proline (Table 1), which is found naturally at low concentrations in mammals [37]. D-alanine and D-asparatate showed greater lifespan extension then their corresponding L-isomers. D-glutamate addition yielded effects on lifespan somewhat similar to its corresponding L-isomer. In contrast to the strong pro-longevity effects observed with L-serine, D-serine supplementation did not lead to lifespan extension at any of the concentrations added and even slightly decreased lifespan at the higher concentrations. And lastly, D-proline supplementation did not extend lifespan as well. These lifespan results are consistent with metabolism of the D-amino acids being required for lifespan extension as D-alanine, D-aspartate, and D-glutamate are present in the E. coli food source and have been shown to be catabolized by the products of the C. elegans genes daao-1, ddo-1, and ddo-3, respectively. D-serine was not found to be present in the E. coli diet, but was instead found to be synthesized endogenously by C. elegans. However, no C. elegans enzyme has yet been found to mediate D-serine [36] or D-proline degradation.

Amino acid-mediated lifespan extension, except when induced by tryptophan, is DAF-16 dependent

To determine if lifespan extension induced by amino acids requires specific longevity pathways, individual amino acids were administered to mutants of known longevity pathways at the concentration that maximally extended lifespan. First, the amino acids alanine, cysteine, glutamine, histidine, lysine, proline, serine, tryptophan, and tyrosine were individually supplemented to short-lived daf-16(mgDf50) mutants (Table 2). DAF-16/FOXO is a central transcription factor that translocates to the nucleus to activate a stress response program in insulin-receptor signaling-deficient worms [38]. Tryptophan was the only supplemented amino acid that extended lifespan in the daf-16 mutant strain indicating tryptophan activates a longevity pathway independent of daf-16, while the other 8 amino acids require DAF-16 mediated gene expression for the increased longevity. Cysteine and histidine even decreased lifespan when supplemented to this strain.
Table 2

The effects of amino acids on lifespan in daf-16 mutant and skn-1 knockdown C. elegans

Strain

Treatment

% of N2 mean lifespan

% of untreated mean lifespan

p-value

# of worms

Replicates

daf-16(mgDf50)

Control

73

 

<0.001

608

7

5 mM histidine

 

92

<0.001

286

2

5 mM proline

 

106

0.0871

133

2

1 mM alanine

 

102

0.111

107

2

1 mM tryptophan

 

118

0.008

183

2

10 mM serine

 

105

0.104

161

2

10 mM glutamine

 

95

0.107

125

2

5 mM cysteine

 

95

0.107

115

2

10 mM cysteine

 

81

<0.001

105

2

5 mM tyrosine

 

96

0.578

140

2

5 mM lysine

 

99

0.907

130

2

N2 (skn-1 RNAi) with live bacteria

Control

59

 

<0.001

156

3

1 mM tryptophan

 

107

0.042

125

3

10 mM serine

 

107

0.01

175

3

5 mM histidine

 

103

0.296

139

3

5 mM proline

 

105

0.088

111

2

N2 with live bacteria

Control

-

  

298

5

1 mM tryptophan

 

109

<0.001

317

5

10 mM serine

 

109

<0.001

375

5

5 mM histidine

 

110

<0.001

277

5

5 mM proline

 

108

<0.001

268

4

To confirm that amino acids activate DAF-16 transcriptional activity, we measured the fluorescence of a sod-3p::gfp DAF-16 reporter strain of worms following culture in the presence of individual amino acids (Figure 2A). As expected from the lifespan data, serine and proline increased fluorescence of these worms. The presence of tryptophan also increased fluorescence, so tryptophan likely activates both DAF-16-dependent and DAF-16-independent pathways for lifespan extension. There was also a strong trend for leucine to increase fluorescence. Unexpectedly, histidine did not increase expression of sod-3p::gfp. The reasons for this finding are unclear as we found that DAF-16 was required for histidine-mediated lifespan extension.
Figure 2

The effects of amino acid addition on DAF-16, SKN-1, and HIF-1-mediated gene expression. (A) The effects of amino acid addition on sod-3p::GFP fluorescence as a measure of DAF-16 transcriptional activity. (B) and (C) The effects of amino acid addition on gst-4p::GFP fluorescence as a measure of SKN-1 transcriptional activity. (D) and (E) The effects of amino acid addition on nhr-57p::GFP fluorescence as a measure of HIF-1 transcriptional activity. 20 μM potassium cyanide was used as a positive control (*p < 0.05).

Most amino acids activate SKN-1 transcriptional activity

The SKN-1/Nrf2 signaling pathway increases cellular antioxidant and detoxification gene expression to extend lifespan. We determined the effect of serine, tryptophan, histidine, or proline addition on lifespan of skn-1 knockdown worms. As shown in Table 2, tryptophan or serine supplementation extended lifespan, but not to the extent as in control worms, while there were only insignificant trends toward increased lifespan following histidine or proline addition.
Table 3

The effects of amino acids on lifespan in aak-2, sir-2.1 and eat-2 mutant and bec-1 knockdown worms

Strain

Treatment

% of N2 control mean lifespan

% of untreated mean lifespan

p-value

# of worms

Replicates

aak-2(gt33)

Control

80

 

<0.001

786

8

5 mM histidine

 

100

0.877

189

2

5 mM proline

 

100

0.919

187

2

1 mM alanine

 

100

0.943

209

2

1 mM tryptophan

 

102

0.060

220

2

10 mM serine

 

101

0.137

204

2

5 mM lysine

 

87

0.373

180

2

5 mM cysteine

 

85

0.952

140

2

10 mM cysteine

 

90

0.122

145

2

5 mM tyrosine

 

80

<0.001

200

2

5 mM glutamine

 

94

0.436

180

2

10 mM glutamine

 

103

0.126

200

2

sir-2.1(ok434)

Control

86

 

<0.001

299

4

5 mM histidine

 

100

<0.830

154

2

5 mM proline

 

104

0.211

114

2

1 mM alanine

 

98

0.225

165

2

1 mM tryptophan

 

102

0.673

121

2

10 mM serine

 

101

0.482

136

2

10 mM glutamine

 

110

<0.001

180

2

5 mM cysteine

 

105

0.244

192

2

10 mM cysteine

 

110

<0.001

190

2

5 mM tyrosine

 

93

0.231

131

2

5 mM lysine

 

107

0.017

146

2

1 mM phenylalanine

 

105

0.049

155

2

10 mM phenylalanine

 

101

0.402

176

2

eat-2(ad1116)

Control

142

 

<0.001

135

2

10 mM serine

 

108

0.078

161

2

1 mM tryptophan

 

105

0.099

138

2

5 mM glutamine

 

100

0.841

134

2

5 mM histidine

 

106

0.091

153

2

5 mM proline

 

107

0.076

176

2

N2 (bec-1 RNAi) with live bacteria

Control

123

 

<0.001

184

2

1 mM tryptophan

 

107

<0.001

162

2

10 mM serine

 

101

0.316

152

2

5 mM histidine

 

99

0.274

117

2

5 mM proline

 

98

0.09

102

2

To further check the ability of amino acids to activate SKN-1, we used a gst-4p::GFP SKN-1 reporter strain of worms (Figure 2B and C). We found that 8 of the 10 amino acids tested that increased lifespan increased GFP expression of the reporter strain. Amino acids that activated gst-4p::GFP expression included serine, proline, glutamine, alanine, leucine, lysine, and tyrosine, while tryptophan and cysteine did not. We also tested the effects of 2 amino acids, phenylalanine and asparagine, which decreased lifespan on the fluorescence of this reporter strain and observed no induction of expression. Overall, there was a small correlation between the amount of SKN-1 activity and the extent of lifespan extension as serine and proline extended lifespan to the greatest extent and also increased fluorescence of the SKN-1 reporter strain to the greatest extent. It has previously been hypothesized that proline catabolism transiently increases ROS production that leads to SKN-1 activation [26]. Our results are consistent with this hypothesis. Cysteine is a strong antioxidant and likely quenched ROS required for SKN-1 activation likely explaining the lack of activation by this amino acid.

The RNAi feeding experiments require live bacteria, while heat-killed bacteria were used in all other lifespan experiments. It is possible that the live bacteria used in the SKN-1 RNAi lifespan experiments metabolized the added amino acids dampening the degree of lifespan extension. Therefore, we performed control experiments supplementing amino acids to C. elegans feeding on live control HT115(DE3) E. coli. C. elegans fed live control bacteria had a mean lifespan of 16.1 +/− 0.2 days, slightly less than worms fed heat-killed bacteria (mean lifespan of 17.2 +/− 0.3 days). Histidine extended lifespan to a similar extent in the presence of live or heat-killed bacteria as shown (Table 2 and Additional file 1: Table S1). However, tryptophan-induced lifespan extension was slightly blunted by the use of live bacteria, and serine or proline-induced lifespan extension was blunted by roughly 50% by the use of live bacteria. A faster rate of E. coli catabolism of serine and proline than tryptophan and histidine likely explain these observations.

Histidine and serine increase HIF-1 target gene expression

The hypoxia-inducible factor-1 (HIF-1) protein is degraded quickly during standard conditions, but is stabilized during hypoxia or by other specific stresses to increase lifespan in C. elegans [39]. Therefore, we tested the HIF-1 reporter strain nhr-57p::GFP [39] for amino acid-induced changes in GFP fluorescence (Figure 2D and E). Cyanide was used as a positive control as it inhibits cytochrome c oxidase, the protein complex which binds molecular oxygen, the terminal electron acceptor in the electron transport chain, to mimic the effects of hypoxia on mitochondria. We found that histidine or serine increased fluorescence, while tryptophan, proline, tyrosine, alanine, cysteine, glutamine, lysine, or leucine did not. These data indicate that stabilization of HIF-1 may be one of the mechanisms through which histidine and serine extend lifespan, although lifespan experiments with HIF-1 mutant worms are needed to confirm this hypothesis.

Amino acid-mediated lifespan extension is AAK-2 (AMPK) dependent

Next we individually administered C. elegans our test set of 10 amino acids except leucine to aak-2(gt33) worms, which are depleted of one of the two catalytic subunits of AMP-activated protein kinase (AMPK) and performed lifespan analysis (Table 3). AMPK signaling inhibits target of rapamycin (TOR) kinase signaling to stimulate autophagy to recycle cellular components. AMPK also stimulates the sirtuin deacetylase SIR-2.1, SKN-1/Nrf2, and DAF-16/FOXO pro-longevity pathways [40]. None of the amino acids extended lifespan in this mutant strain. Tyrosine decreased lifespan while the other 8 amino acids tested had no significant effect. Therefore, AAK-2 is required for the longevity benefits provided by the amino acids.
Table 4

The effects of amino acids on lifespan of rsks-1 , gcn-2 , ife-2 , gas-1 , and mev-1 mutants

Strain

Treatment

% of N2 control mean lifespan

% of untreated mean lifespan

p-value

# of worms

Replicates

rsks-1(ok1255)

Control

109

 

<0.001

362

4

1 mM tryptophan

 

71

<0.001

130

2

5 mM histidine

 

93

0.031

135

2

5 mM proline

 

94

0.042

140

2

10 mM serine

 

101

0.236

162

2

gcn-2(ok871)

Control

90

 

<0.001

479

4

1 mM tryptophan

 

99

0.489

160

2

5 mM histidine

 

100

0.335

163

2

5 mM proline

 

107

0.001

205

2

10 mM serine

 

104

0.006

183

2

Ife-2(ok306)

Control

97

 

0.245

112

2

1 mM tryptophan

 

94

0.029

138

2

5 mM histidine

 

98

0.597

110

2

5 mM proline

 

102

0.352

117

2

10 mM serine

 

99

0.791

96

2

gas-1(fc21)

Control

69

 

<0.001

119

2

5 mM histidine

 

104

0.092

110

2

10 mM serine

 

98

0.327

106

2

5 mM proline

 

109

0.003

115

2

mev-1(kn1)

Control

69

 

<0.001

273

2

5 mM histidine

 

104

0.021

215

2

10 mM serine

 

109

<0.001

258

2

5 mM proline

 

102

0.102

256

2

Many amino acids require SIR-2.1 for lifespan extension

Next the effects of individual supplementation of these same 9 amino acids as well as phenylalanine on lifespan of the sir-2.1(ok434) NAD-dependent sirtuin deacetylase mutant were determined (Table 3). Small to moderate lifespan increases occurred with cysteine, glutamine, lysine, and low dose phenylalanine supplementation, but there were no significant effects of 6 other amino acids tested on the lifespan of this strain. Therefore SIR-2.1 was required for lifespan extension mediated by slightly more than half of the amino acids tested. Surprisingly, high dose (10 mM) phenylalanine supplementation did not lead to a decreased lifespan in this strain as it did in the N2 control worms.

Amino acids do not significantly extend lifespan in long-lived DR worms

Restricting a specific amino acid such as methionine from the diet can be utilized to extend lifespan and gain some of the benefits of dietary restriction (DR) [8], but there is not much evidence that specific amino acid supplementation can yield enhanced longevity effects. Therefore, we administered individual amino acids to eat-2(ad1116) mutants that are dietarily restricted and long-lived because of reduced pharyngeal pumping. The non-treated control eat-2 mutants had a mean lifespan 42% longer than N2 controls indicating that our control worms were not dietarily restricted under our growth conditions. None of the 5 amino acids tested yielded statistically significant lifespan extension (Table 3). However, 4 of the amino acids yielded strong trends toward lifespan extension (p-values between 0.08 and 0.10). Therefore the individual amino acids are likely utilizing some portion of the DR signaling pathway for lifespan extension.

Autophagy is required for the lifespan extension induced by serine, proline, or histidine supplementation, but not by tryptophan

Since autophagy has been shown to be required for DR-mediated lifespan extension [41], we determined if autophagy was also required for amino acid-mediated longevity. To block autophagy we knocked down bec-1, the C. elegans Beclin-1 homolog and monitored lifespan following supplementation with serine, proline, histidine, or tryptophan. Knockdown of bec-1 by RNAi feeding increased lifespan as has previously been shown in [42] and prevented lifespan extension induced by supplementation with serine, proline or histidine, but not by tryptophan (Table 3). Therefore, the majority of amino acids, but not tryptophan, require autophagy for lifespan extension, once again suggesting that tryptophan extends lifespan through a mechanism distinct from other amino acids.

The PHA-4/FOXA transcription factor is required for induction of autophagy and lifespan extension in response to DR. In addition, expression of the PHA-4 transcription factor has been shown to be upregulated by roughly 50% by DR [43]. Therefore, we determined if individual amino acid administration could increase PHA-4 protein levels by using a strain of worms engineered to express PHA-4:GFP:3xFLAG using the endogenous pha-4 promoter [44]. Surprisingly, we found that serine, histidine, or tryptophan addition did not alter the GFP fluorescence of this strain (Additional file 4: Figure S3). However, leucine addition resulted in a strong trend toward increased fluorescence (p = 0.08). On the whole, individual amino acid supplementation did not appear to have much of an effect on fluorescence in this strain. However, we cannot yet rule out the possibility that changes in PHA-4 localization or post-translational modification play a role in individual amino acid-induced longevity. It is also possible that the added GFP and FLAG tags affect the stability of the protein. Lifespan studies using pha-4 RNAi are needed to determine a role, if any, for PHA-4 in amino acid-mediated lifespan extension.

Inhibition of TOR signaling plays a role in amino acid-mediated lifespan extension

Specific amino acids, most notably leucine, but also to a lesser extent arginine and glutamine can be activators of the TOR signaling pathway that limits lifespan [45]. Administering rapamycin, a TOR inhibitor, or feeding TOR RNAi to C. elegans induces autophagy and extends lifespan [46,47]. More recently it was found that alpha-ketoglutarate supplementation can lead to TOR inhibition to extend lifespan [48]. Knockout or knockdown of the ribosomal S6 kinase, which is downstream of TOR kinase in the signaling pathway, also extends lifespan [49]. Part of this effect may rely on a decreased rate of protein translation as inhibitors of protein translation can also extend lifespan [49]. Therefore, we determined the effects of specific amino acids on lifespan in long-lived rsks-1(ok1255) ribosomal S6 kinase mutants, where this arm of the TOR signaling pathway is inhibited (Table 4). Unlike the results with N2 control worms, addition of serine did not alter the lifespan of this strain, while proline or histidine addition slightly decreased lifespan, and tryptophan addition decreased lifespan by 20%. Therefore, these amino acids appear to use inhibition of TOR signaling to mediate lifespan extension, as the amino acids did not extend lifespan in long-lived mutant worms where TOR signaling was already disrupted.

A decreased rate of translation is required for the full lifespan extending effects of amino acids

GCN-2 (general control nonderepressible-2) kinase can slow the rate of translation initiation by phosphorylating eukaryotic translation initiation factor-2 alpha (eIF-2α) when tRNAs become uncharged due to low amino acid levels [34] or in times of mitochondrial metabolic stress [33]. We hypothesized that amino-acid supplementation causing amino acid imbalance could result in inefficient tRNA charging or cause metabolic stress signaling through GCN-2 to extend lifespan. Therefore, we determined the lifespan of gcn-2(ok871) mutants supplemented with individual amino acids (Table 4). We found that histidine or tryptophan supplementation did not lead to increased longevity when using this strain, while only a 4% or 7% lifespan extension occurred when serine or proline, respectively, were supplemented. To further determine a role for decreased translation in amino acid imbalance-mediated longevity, we performed lifespan analysis using the ife-2(ok306) strain [50], which is deficient in an isoform of the translation initiation factor eIF4E and shown to be long-lived. Surprisingly, under our liquid culture conditions using heat-killed bacteria as food, the lifespan of this strain was not significantly different than the control. However, supplementation of serine, proline, histidine, or tryptophan to this strain did not lead to extended lifespan, while tryptophan addition even slightly decreased lifespan. Therefore signaling to slow the rate of translation is likely a general mechanism involved in individual amino acid-mediated increased longevity.

The effect of individual amino acids on the lifespan of mitochondrial ETC complex I and II mutants

To test the hypothesis that mitochondrial ETC activity is important for amino-acid induced lifespan extension we supplemented serine, histidine, or proline to either short-lived mitochondrial ETC complex I defective gas-1(fc21) mutant worms or to short-lived mitochondrial ETC complex II defective mev-1(kn1) mutant worms (Table 4). We found that proline supplementation extended the lifespan of gas-1 mutants, but that serine or histidine were unable to extend lifespan, although there was a strong trend with histidine (p = 0.09). When we supplemented each of these 3 amino acids to mev-1 mutants, we found opposite effects. Proline did not extend lifespan, although a strong trend was observed (p = 0.10), while serine and histidine extended lifespan. Therefore normal complex I (NADH dehydrogenase) activity is required for the full serine and histidine-mediated lifespan extension, while normal complex II activity is required for proline-mediated lifespan extension. This data may be explained in that proline dehydrogenase generates FADH2 which feeds electrons into the ETC at complex II and histidine and serine catabolism generates NADH that feeds electrons into the ETC at complex I.

Most supplemented metabolites extended lifespan at an optimal concentration

Since supplementation with an optimal concentration of most amino acids extended the lifespan of the worms, it is possible that their breakdown to TCA cycle intermediates may play a role in lifespan extension. It has previously been shown that supplementation with pyruvate [51], acetate (that can be readily metabolized to the TCA cycle substrate acetyl-CoA) [52], or the TCA cycle intermediates malate, fumarate [53], oxaloacetate [54], and alpha-ketoglutarate [48] extended lifespan in C. elegans. We therefore determined the lifespan of the worms individually supplemented with 1, 5, or 10 mM concentrations of the TCA cycle intermediates citrate, isocitrate, alpha-ketoglutarate, or succinate (Table 5). We previously found that 10 mM succinate did not extend lifespan, but did induce translocation of the pro-longevity factor DAF-16 to the nucleus [53]. But here we find that lowering the concentration of succinate to 5 mM or 1 mM resulted in lifespan extension (Figure 3A), consistent with a recent report of a longevity benefit [48]. Citrate is present at 10 mM in all of our experiments as a standard buffer component of the S-medium. We found that removing it did not affect the lifespan (Figure 3B). Previous findings also failed to find an extension of lifespan with citrate supplementation [48,52]. We found that alpha-ketoglutarate at any of the 4 concentrations tested from 0.1 to 10 mM extended lifespan (Figure 3C), as recently reported for an 8 mM dose [48]. Adding DL-isocitrate to the medium led to an increase in lifespan at the 5 mM concentration, but a decrease in lifespan at the 10 mM concentration (Figure 3D). It is unknown if the non-naturally occuring L-isomer contributed to this effect, but since we found the non-naturally occurring isomer D-malate to decrease lifespan at all 3 concentrations tested (Table 5), it is a strong possibility. Another group observed no effect of 8 mM isocitrate on lifespan [48]. Therefore, of the 7 TCA cycle intermediates that we have tested, 6 were able to extend lifespan at an optimal dose.
Table 5

The effects of TCA cycle intermediates and their isomers on C. elegans lifespan

Treatment

Concentration

% of untreated mean lifespan

p-value

# of worms

Replicates

succinate

1 mM

111

<0.001

590

4

5 mM

110

<0.001

570

4

10 mM

104

0.098

607

4

citrate1

10 mM

98

0.414

229

2

α-ketoglutarate

0.1 mM

110

<0.001

261

3

1 mM

115

<0.001

345

3

5 mM

111

<0.001

337

3

10 mM

107

0.042

333

3

DL-isocitrate

1 mM

103

0.202

452

4

5 mM

113

<0.001

523

4

10 mM

72

<0.001

217

4

D-malate

1 mM

85

<0.001

106

1

5 mM

76

<0.001

77

1

10 mM

79

<0.001

142

1

1compared to a medium lacking citrate. All other experiments contain 10 mM citrate as part of the standard culture media.

Figure 3

Individual supplementation of many TCA cycle metabolites extends mean lifespan in C. elegans . (A) Succinate extends lifespan, (B) citrate does not extend lifespan, (C) alpha-ketoglutarate extends lifespan, and (D) isocitrate extends lifespan at one or more of the concentrations tested. 10 mM citrate is a standard component of the S-medium. It was removed to determine the effect of citrate on lifespan.

We hypothesized that catabolism of the amino acids for anaplerosis or energy production was likely playing a role in the lifespan extension. If this is true supplementing other common cellular metabolites should also extend lifespan. Therefore, we performed lifespan analysis of worms supplemented with sugars or other metabolites lacking nitrogen atoms (Additional file 5: Table S2). At an optimal dose gluconate, glycerol, inositol, phophoenolpyruvate, or ribose substantially increased lifespan, while xylose, galactose, DL-lactate, or caprylate just slightly increased lifespan. Glucuronolactone, glyceraldehyde, fructose, propionate, or dihydroxyacetone did not extend lifespan and the last 4 of these compounds even decreased lifespan by 13-25% at the 10 mM dose. Glyceraldehyde, fructose, and dihydroxyacetone are readily converted into glycolytic intermediates leading to the formation of toxic methylglyoxyl from glyceraldehyde phosphate or dihydroxyacetone phosphate, which could contribute to their toxicity, while propionic acid is known to be neurotoxic at high levels [28].

Since many amino acids activated SKN-1, while TCA cycle intermediates did not, we hypothesized that nitrogen-containing metabolites might be slightly more potent inducers of lifespan extension. The effects of many nitrogen-containing metabolites on lifespan are shown in Additional file 6: Table S3. At an optimal dose carnosine, beta-alanine, betaine, homocysteine, ornithine, agmatine, putrescine, taurine, and theanine extended lifespan. For the majority of these compounds, the lowest concentration, such as 1 mM, yielded greater lifespan extension than the highest 10 mM concentration suggesting a hormetic dose response. Supplementation with creatine, or the histidine catabolites histamine or urocanic acid did not extend lifespan at any of the 3 concentrations tested. Although most of the nitrogen-containing compounds extended lifespan at an optimal dose, the extent of lifespan extension was not noticeably different than when supplementing with compounds lacking nitrogen.

C. elegans lifespan was not limited by nitrogen availability

We used heat-killed E. coli as a food source to prevent the bacteria from metabolizing the added metabolites, but we have found that heat-killing E. coli causes the loss of one or more essential growth-limiting nutrients during heating. So lowering the concentration of heat-killed bacteria in the growth media by just a factor of 2 did not allow completion of larval growth into adulthood, but instead led to dauer formation. The concentration of live bacteria could be reduced by 30–40 fold before dauer formation during larval development. To test if the worms may have been nitrogen limited under our culture conditions, we supplemented the worms with peptone or other nitrogen containing compounds and measured the lifespan. Interestingly, peptone at 1.25 g/L, half the concentration present in nematode growth media (NGM) decreased lifespan by 22% (Additional file 6: Table S3). This concentration contains roughly 10 mM total amino acids. These results support published findings where 5 g/L (2x NGM) and 10 g/L (4x NGM) peptone also decreased C. elegans lifespan in liquid S medium [55]. Lowering the peptone concentration to 0.125 g/L (0.1x NGM) yielded a similar lifespan as untreated controls. We next added ammonium chloride as a nitrogen source. Concentrations of ammonium chloride from 1 to 10 mM did not extend lifespan. So amino acids do not increase lifespan solely by providing nitrogen to the worms.

Phenylalanine and alpha-ketoglutarate activate a HSF-1 reporter strain

Since supplementation of many of the amino acids and other metabolites showed less lifespan extension at higher concentrations, we hypothesized that C. elegans mounted a stress response that resulted in lifespan extension at lower amino acid levels, but at higher levels the stress response was overwhelmed leading to decreased lifespan. Therefore, we determined if amino acid supplementation activates a Phsp-16.2::GFP heat shock reporter strain of worms. HSP-16.2 is a small cytoplasmic heat shock protein and target of the HSF-1 transcription factor [56]. We first tested the effects of glutamine, histidine, methionine, serine, tryptophan, or tyrosine, amino acids that extended lifespan, or phenylalanine, an amino acid that decreased lifespan on GFP fluorescence in the Phsp-16.2::GFP reporter strain using heat shock as a positive control (Figure 4A). Of these amino acids, only phenylalanine activated GFP reporter gene expression.
Figure 4

The effects of amino acids on heat shock, mitochondrial unfolded protein response, and ER stress response. Amino acids were added at the concentration tested that yielded maximal lifespan extension except phenylalanine, which did not extend lifespan. (A) Phsp-16.2::GFP (B) Phsp-4::GFP (C) Phsp-6::GFP (D) Phsp-60::GFP. For panels A and B heat shock at 35°C for 2 hours was used as a positive control. For panels C and D 50 μg/ml ethidium bromide treatment for 2 days was used as a positive control (*p < 0.05 vs. control).

We next tested the effects of TCA cycle intermediate or pyruvate supplementation on the Phsp-16.2::GFP reporter strain, as amino acids are broken down into TCA cycle intermediates when they are present in excess. When administered to the Phsp-16.2::GFP reporter strain alpha-ketoglutarate, but none of the other TCA cycle intermediates supplemented increased GFP fluorescence (Figure 5A). Many of the amino acids showing the largest stimulatory effects on lifespan (proline, arginine, histidine, glutamine, and glutamate) are catabolized through glutamate into alpha-ketoglutarate in the TCA cycle.
Figure 5

The effects of TCA cycle metabolites and pyruvate on heat shock, mitochondrial unfolded protein response, and ER stress response. (A) Phsp-16.2::GFP (B) Phsp-4::GFP (C) Phsp-6::GFP (D) Phsp-60::GFP (*p < 0.05 vs. control). For panels A and B heat shock at 35°C for 2 hours was used as a positive control. For panels C and D 50 μg/ml ethidium bromide treatment for 2 days was used as a positive control (*p < 0.05 vs. control).

Histidine, tryptophan, and citrate induce an ER stress response

We next determined if amino acids activated the endoplasmic reticulum (ER) stress response by using a reporter strain of worms engineered to contain a heat shock protein-4 (hsp-4) promoter driving expression of green fluorescent protein (GFP) [57]. We tested the effect of glutamine, histidine, methionine, serine, tryptophan, or tyrosine supplementation on expression of GFP in the Phsp-4::GFP reporter strain of worms using heat shock as a positive control (Figure 4B). Histidine and tryptophan induced GFP expression, methionine and glutamine reduced GFP expression, while the other amino acids had no effect.

Subsequently we determined the effects of supplemented TCA cycle intermediates and pyruvate on the Phsp-4::GFP ER stress response reporter strains of worms (Figure 5B). Citrate activated Phsp-4::GFP reporter gene expression, and there was also a strong trend (p = 0.05) for increased expression with alpha-ketoglutarate, while the other TCA cycle intermediates had no effect. Chelation of calcium or other metal ions is a possible mechanism as to how some of these compounds or their metabolites activate ER stress.

Tryptophan induces the mitochondrial unfolded protein response

We further tested for activation of the mitochondrial unfolded protein response using Phsp-6 and Phsp-60 reporter strains and ethidium bromide treatment as the positive control. HSP-6 is the worm homolog of mammalian mitochondrial hsp-70, while HSP-60 is also localized to the mitochondrion. Both mitochondrial heat shock proteins play a role in the mitochondrial unfolded protein response, but this response is not always associated with longevity [58]. For the Phsp-6::GFP reporter strain we tested glutamine, histidine, serine, phenylalanine, and tryptophan (Figure 4C). We found phenylalanine and tryptophan to robustly increase expression, while the other amino acids did not increase expression. We further tested the effects of glutamine, histidine, phenylalanine, proline, serine, tryptophan, and tyrosine on GFP expression in the Phsp-60::GFP reporter strain (Figure 4D). We found only tryptophan to increase expression. There was also a strong trend for proline to increase expression (p = 0.06), while serine slightly decreased expression. Overall, most amino acids do not rely upon the mitochondrial unfolded protein response pathway for lifespan extension.

Next, we determined the effects of the TCA cycle intermediates and pyruvate on the mitochondrial unfolded protein response reporter strains. None of the metabolites affected expression of the Phsp-6::GFP reporter (Figure 5C), while pyruvate, succinate, and malate slightly decreased expression of the Phsp-60::GFP reporter strain (Figure 5D). Overall, the data suggest that TCA cycle intermediate supplementation does not require the mitochondrial unfolded protein response pathway for lifespan extension.

Tryptophan metabolites nicotinic acid, nicotinamide, and picolinic acid induce both ER stress and mitochondrial unfolded protein responses

Since tryptophan activated expression of the ER stress response and 2 mitochondrial unfolded protein response reporter strains, we determined if one or more of its breakdown products or structurally related metabolites could also induce these responses. Therefore we added many of the tryptophan degradation products or tryptophan-related cellular metabolites including serotonin, anthranilic acid, nicotinic acid, nicotinamide, NAD, glutaric acid, kynurenic acid, quinolinic acid, and picolinic acid to the HSF-1 reporter strain, the ER stress reporter strain, and the 2 mitochondrial unfolded protein response reporter strains (Figure 6A-D). Strikingly, nicotinic acid activated expression of the same ER stress response and mitochondrial unfolded protein response reporters as tryptophan, while picolinic acid and nicotinamide activated expression of all 4 GFP reporter strains, although activation of hsp-60::GFP by nicotinamide was low (p = 0.07). Picolinic acid is an isomer of nicotinic acid and an important endogenous metal chelator [59]. Quinolinic acid induced expression of the 2 non-mitochondrial heat shock protein reporters. Therefore, we performed lifespan experiments adding 1 mM picolinic acid or 1 mM quinolinic acid to the culture medium (Additional file 6: Table S3). Picolinic acid addition showed a trend (p = 0.13) toward increased lifespan. In contrast, quinolinic acid addition decreased worm lifespan by 26%, as might be expected from its known neurotoxicity [60]. NAD precursors have previously been shown to induce the mitochondrial unfolded protein response [61]. Here, we added a 0.1 mM dose of NAD and found it to only activate expression of hsp-4, the marker of ER stress. Although tryptophan metabolic byproducts could contribute to the protective effects of supplemental tryptophan, others have shown data suggesting that tryptophan itself may be the protective metabolite in a C. elegans model of alpha-synuclein toxicity [27].
Figure 6

The effects of tryptophan metabolites on heat shock, mitochondrial unfolded protein response, and ER stress response. (A) Phsp-16.2::GFP (B) Phsp-4::GFP (C) Phsp-6::GFP (D) Phsp-60::GFP (*p < 0.05 vs. control). For panels A and B heat shock at 35°C for 2 hours was used as a positive control. For panels C and D 50 μg/ml ethidium bromide treatment for 2 days was used as a positive control (*p < 0.05 vs. control).

Proline and tryptophan increase C. elegans thermotolerance

Amino acids could have induced expression of other heat shock or stress-inducible genes to extend lifespan not assayed in our reporter experiments described above. Therefore, we determined the effect of individual amino acid supplementation on the thermotolerance of C. elegans. We supplemented the growth medium with glutamine, histidine, proline, serine, or tryptophan and monitored the viability of the worms following transfer from 20°C to 35°C (Table 6 and Additional file 7: Figure S4A). Proline provided a 30% increase in thermotolerance and tryptophan provided a 10% increase in thermotolerance, while there was no significant effect of the other amino acids. The effect of proline is not too surprising given that proline stabilizes proteins and membranes and is overproduced to protect plants and some microorganisms from osmotic, salinity, and temperature stresses [62].
Table 6

The effects of amino acids on C. elegans thermotolerance

Treatment

% of untreated mean survival

p-value

# of worms

Replicates

5 mM histidine

102

0.494

229

2

1 mM tryptophan

110

<0.001

208

2

10 mM serine

102

0.794

196

2

5 mM proline

130

<0.001

200

2

5 mM glutamine

99

0.584

82

1

We next monitored the resistance to oxidative stress by monitoring the viability of worms following administration of paraquat (Additional file 7: Figure S4B). Paraquat is an inducer of superoxide production through redox cycling. None of the tested amino acids including proline, serine, histidine, tryptophan, or leucine significantly protected the worm viability against this stress, although there was a strong trend for protection with histidine (p = 0.08).

Little effect of amino acid supplementation on Alzheimer’s amyloid-beta toxicity

Since many of the amino acids extended lifespan when they were supplemented to the culture medium, we also determined if individual amino acid supplementation could delay toxicity in C. elegans models of human neurodegenerative disorders. We first determined the effects of serine, histidine, proline, tryptophan, or methionine supplementation on the rate of paralysis development when the amyloid-beta peptide, which builds up in Alzheimer’s disease brain, is expressed in worm body wall muscle from a temperature-inducible promoter [63]. Overall, amino acid supplementation only had a minimal effect on the rate of paralysis. We found that serine (p = 0.07) (Figure 7A) or histidine (p = 0.05) (Figure 7B) supplementation gave strong trends to delay muscle paralysis, while no significant effects were found with proline, methionine, or tryptophan (Additional file 8: Table S4).
Figure 7

Amino acids do not provide much protection in models of proteotoxicity. (A) Serine and (B) histidine supplementation yield slight protection against muscle amyloid-beta toxicity. (C) Tryptophan supplementation decreases alpha-synuclein aggregate fluorescence. (D) Amino acid supplementation does not protect against TDP-43 toxicity.

Tryptophan protects from alpha-synuclein and polyglutamine toxicity

We next determined the effects of supplementation with histidine, proline, serine, or tryptophan on alpha-synuclein aggregation in worms expressing an alpha-synuclein-green fluorescent protein fusion (Figure 7C). Alpha-synuclein aggregates into Lewy bodies in the substantia nigra region of the brain in Parkinson’s disease. Tryptophan was highly protective giving a 17% reduction in aggregate fluorescence, while the other amino acids were without effect. We also tested the effects of tryptophan, serine, and proline on aggregates formed from the expression of a polyglutamine (Q35)–GFP fusion protein [64] (Additional file 9: Figure S5) as a model of the proteotoxicity that occurs in Huntington’s disease and other polyglutamine trinucleotide expansion disorders. We found a strong trend toward a decreased number of aggregates with the addition of tryptophan (p = 0.07), but no significant effect of the other two amino acids tested. It is not surprising that tryptophan supplementation was protective in these C. elegans proteotoxicity models as depletion of the TDO-2 enzyme that degrades tryptophan has been shown to increase worm tryptophan levels and be protective in several worm models of proteotoxicity [27]. It was also shown that tryptophan supplementation was able to increase the motility of Q40 polyglutamine expressing worms.

Alpha-ketoglutarate, but not amino acids, protects C. elegans expressing TDP-43

Tar DNA-binding protein-43 (TDP-43) is mostly a nuclear protein under normal conditions, but cytoplasmic accumulation is associated with ALS and other neurodegenerative diseases. Overexpression of TDP-43 leads to toxicity in C. elegans and is used as an ALS model. We therefore tested if several amino acids including histidine, methionine, proline, serine, and tryptophan could alter the reduced lifespan of TDP-43 overexpressing worms (Figure 7D and Additional file 10: Table S5). However, none of these amino acids protected against the reduced lifespan, while histidine addition even further reduced the lifespan. But, we did find a protective effect of alpha-ketoglutarate supplementation in this model, supporting data from a study in which alpha-ketoglutarate in combination with other metabolites was protective in the SOD1-G93A mouse model of ALS [65].

Serine and tryptophan partially block lifespan reduction in high glucose culture media

High glucose in the bloodstream is a marker of insulin resistance and diabetes and high levels of glucose in C. elegans culture medium is known to reduce lifespan [66,67]. Therefore high glucose supplementation has been used as a model of diabetes in C. elegans. Since alterations of amino acid levels also accompany diabetes, we determined if select amino acids could alter the decreased lifespan resulting from the addition of 50 mM glucose to the culture medium. We found glucose addition decreased lifespan by 30 percent and that serine (Figure 8A) or tryptophan (Figure 8B) supplementation partially blocked lifespan reduction. Histidine, proline, or tyrosine addition had no significant effect, while glutamine addition decreased lifespan to a greater extent than glucose by itself (Additional file 11: Table S6).
Figure 8

Serine or tryptophan partially prevent high glucose from reducing C. elegans lifespan. (A) Serine extends C. elegans lifespan in the presence of high glucose (p < 0.001). (B) Tryptophan extends C. elegans lifespan in the presence of high glucose (p < 0.001).

Amino acid supplementation does not significantly alter C. elegans oxygen consumption and ATP levels

Since amino acid supplementation may transiently increase ROS production for the activation of SKN-1, we hypothesized that the added amino acids may be catabolized to increase mitochondrial ETC function. Therefore we measured worm oxygen consumption and ATP levels. However, we did not find significantly altered oxygen consumption or ATP levels following addition of the individual amino acids serine, proline, histidine, tryptophan, leucine, asparagine, or phenylalanine to the worms (Additional file 12: Figure S6). Therefore, the supplemented amino acids are either not being metabolized at a substantial rate or are being metabolized in replacement of respiratory substrates present in the E. coli food source preventing an overall increase in metabolic rate.

Discussion

Individual supplementation with 18 of the 20 proteogenic amino acids at an optimal concentration increased the lifespan of C. elegans. This metabolite-induced lifespan extension was not specific for only amino acids as supplementation with TCA cycle intermediates and many different classes of cellular metabolites also led to significant lifespan extension, suggesting altered cellular metabolism or TCA cycle anaplerosis plays a prominent role. Of the 20 amino acids, serine and proline extended lifespan to the largest extent. Strikingly, these and other top amino acids did not significantly extend the lifespan of long-lived dietary restricted eat-2 mutants. If similar effects occurred in humans, imbalanced amino acid diets could be developed as a dietary restriction mimetic to delay aging and aging-related disease. In this regard a methionine restricted diet has been used clinically to treat metabolic syndrome [68]. However, whether or not amino acid supplementation strategies will apply to higher eukaryotes remains to be determined as individual supplementation of methionine failed to extend the lifespan of fruit flies [24], while supplementation of methionine decreased the lifespan of mice [69].

Individual amino acid supplementation may decrease the rate of translation to extend lifespan

Most of the well-studied longevity pathways in C. elegans such as DAF-16, SKN-1, AAK-2, SIR-2.1, and HIF-1 appear to be involved in the lifespan extension mediated by histidine, serine, and proline, with the exception of the HIF-1 pathway for proline. However, tryptophan extends lifespan in a SKN-1 and DAF-16 independent manner, although tryptophan did increase fluorescence of a DAF-16 reporter strain of worms. These different longevity pathways may converge to decrease the rate of translation by the ribosome for lifespan extension. A small to moderate amount of amino acid imbalance could hinder correct aminoacyl-tRNA synthetase charging of tRNAs slowing the rate of translation in a GCN-2 dependent manner to increase lifespan, while a higher amount of amino acid imbalance may lead to a toxic reduction in translation rates decreasing lifespan. Previously, a decreased rate of translation has been shown to be essential for lifespan extension in mitochondrial mutants [33], during TOR inhibition, or during dietary restriction [34]. Furthermore, long-lived daf-2 mutants were also shown to have a reduced rate of translation [70]. Reduced mitochondrial translation causing mitonuclear protein imbalance has also been shown to lead to increased lifespan [71]. High rates of translation during aging may overwhelm protein chaperone systems resulting in proteotoxicity. Slowing translation or increasing heat shock protein activity may delay this proteotoxicity to increase longevity.

The branched chain amino acid leucine most strongly activates TOR kinase, which can increase the rate of translation and lead to decreased lifespan. Therefore, we were surprised to find that supplementation with 1 mM leucine greatly increased lifespan. In fact, leucine was the second most potent amino acid at this concentration for promoting longevity. Under our standard growth conditions TOR signaling may already be highly activated by amino acids present in the bacterial food source and so may not be able to be further activated. Instead, we hypothesize that leucine metabolism or the amino acid imbalance caused by excess leucine may have activated other signaling pathways leading to TOR inhibition. In this regard, the lack of lifespan extension by amino acids in rsks-1 mutants suggests that individual amino acid supplementation inhibits TOR signaling to extend lifespan. Of the other two branched chain amino acids, valine supplementation showed similar lifespan trends as leucine, even though it is not a potent inducer of TOR activity, and isoleucine supplementation showed little effect on lifespan. At higher concentrations, branched chain amino acids did not affect lifespan as much as at the lower concentrations. Therefore, high levels of branched chain amino acids do not always directly correlate with lifespan extension. Consistent with this hypothesis, decreased levels of branched chain amino acids were found in long-lived Ames dwarf mice [72]. However, amino acid imbalance cannot explain the increased longevity conferred upon supplementation with many other diverse cellular metabolites. Therefore, TCA cycle anaplerosis leading to a reprogramming of mitochondrial metabolism may be the molecular mechanism responsible for lifespan extension.

NAD precursors and tryptophan induce the ER stress response and the mitochondrial unfolded protein response

Another significant finding in this report is that supplementation with tryptophan, nicotinamide, nicotinic acid, or its isomer picolinic acid resulted in the activation of both the mitochondrial unfolded protein and the ER stress response pathways, while NAD addition induced only the ER stress response. In mouse muscle and heart, decreased nuclear NAD levels with aging cause a hypoxia inducible factor-1α (HIF-1α)-induced decrease in mitochondrial transcription leading to mitochondrial dysfunction that was reversed by supplementation with an NAD precursor [73]. In addition to reversing this aging-induced mitochondrial dysfunction, supplementing NAD precursors (or tryptophan) can further protect cells by inducing an ER stress response and a mitochondrial unfolded protein response, although it has already been shown that NAD precursors induce a mitochondrial unfolded protein response [61]. Picolinic acid is a strong metal chelator that is frequently taken with chromium as a possible treatment for metabolic syndrome, although the efficacy of this treatment has been questioned [74]. But picolinic acid itself has been shown to be neuroprotective [59]. It will be important to determine if the protective effects of picolinic acid are due to metal chelation and if picolinic acid, nicotinic acid, and nicotinamide also induce the ER stress response or mitochondrial unfolded protein response in mammalian cells.

Is catabolism of amino acids important for their longevity effects?

The catabolism of supplemented amino acids likely mediates their effects on longevity, but there are likely exceptions to this rule. We were surprised to find no increase in oxygen consumption or ATP levels as markers of increased metabolism when amino acids were added to the culture medium. It was previously shown that proline catabolism and the resulting transient increase in ROS production by the electron transport chain were essential for its pro-longevity effects [26]. Most other amino acids may also be metabolized to emit a transient ROS signal leading to SKN-1 dependent lifespan extension. Possible evidence for this includes that enzymes for proline, tryptophan, phenylalanine, glutamine, and D-alanine degradation are upregulated in long-lived daf-2 insulin receptor mutant worms [26], where SKN-1 is also activated [75].

However, alpha-ketoglutarate-mediated lifespan extension was shown to be independent of ROS production [48]. Therefore more downstream TCA cycle catabolites such as alpha-ketoglutarate, succinate, malate, and fumarate extend lifespan through SKN-1independent, but DAF-16 dependent mechanisms [53]. In addition, cysteine and tryptophan-induced lifespan extension were independent of SKN-1, so supplementation with these amino acids did not likely alter mitochondrial metabolism to increase ROS production. Consistent with this, knockdown of the tryptophan 2,3-dioxygenase (TDO-2) enzyme that degrades tryptophan led to increased lifespan and increased tryptophan levels, but no changes in the levels of many of the downstream metabolites of tryptophan degradation suggesting that increased tryptophan levels and not altered levels of the catabolic byproducts were responsible for the increased lifespan and protection from proteotoxicity [27].

Future studies will aim to determine the metabolic mechanisms through which amino acids activate SKN-1 activity and through which serine and histidine activate HIF-1. For example, enzyme knockdown studies using RNAi may be used to determine whether serine catabolism is required for serine-mediated lifespan extension, as serine can be directly deaminated to pyruvate, which extends lifespan [51]. However, serine can also be used as a one-carbon donor for methylation events such as histone methylation, which can alter gene expression patterns leading to increased longevity as well [76].

TCA cycle metabolism and longevity

Different amino acids are catabolized and enter the TCA cycle through different intermediates of the cycle. We did not find that the amino acids yielding the greatest effects on lifespan were degraded through one common catabolic pathway. Additional file 13: Figure S7, Additional file 14 Figure S8, and Additional file 15: Figure S9 show the specific TCA cycle intermediate into which each of the amino acids is catabolized and how lifespan was affected by 1 mM, 5 mM, and 10 mM amino acid concentrations, respectively. As mentioned previously, the only trend in the data set is that amino acids broken down into alpha-ketoglutarate yielded larger than average lifespan extensions. However, this cannot explain the large lifespan extension induced by serine addition, which is catabolized to pyruvate. Surprisingly, we previously discovered that malate or fumarate supplementation increased total pyridine (NAD + NADH) nucleotide levels and also induced mild mitochondrial uncoupling increasing the NAD/NADH ratio, both of which may have been involved in the lifespan extension induced by these TCA cycle intermediates [53]. Catabolism of other metabolites may result in similar effects.

Knockdown of mitochondrial aconitase or a subunit of mitochondrial NAD-dependent isocitrate dehydrogenase increased lifespan in C. elegans [77]. The increased longevity of these mutants is likely due in part to decreased flux through this portion of the TCA cycle leading to increased NAD levels, which has been shown to extend lifespan [78]. The isocitrate dehydrogenase and alpha-ketoglutarate dehydrogenase enzymes reduce mitochondrial NAD to NADH. Citrate supplementation may not increase lifespan due to the increased flux through this portion of the TCA cycle leading to a decrease in NAD levels, although in the cytoplasm citrate is metabolized to acetyl-CoA that has been shown to inhibit autophagy, which can also prevent lifespan extension [79]. However, isocitrate supplementation would also not be expected to increase longevity as its normal metabolism is predicted to lower NAD levels. However, there is also an NADP-dependent isocitrate dehydrogenase isoform present that may help prevent declines in NAD levels and allow for isocitrate-mediated lifespan extension at least in a narrow range of concentrations.

It is possible that supplementation with amino acids broken down into alpha-ketoglutarate may extend lifespan by running isocitrate dehydrogenase in the opposite direction of its normal mode to oxidize NADH to NAD while alpha-ketoglutarate and carbon dioxide are metabolized into isocitrate. Some cancer cells have been shown to use this metabolism when oxidizing glutamine as a primary energy substrate [80]. The citrate produced from isocitrate is then exported to the cytoplasm where acetyl-CoA and oxaloacetate are formed by ATP citrate lyase. This metabolic flexibility in TCA cycle metabolism may be required for specific amino acid and TCA cycle metabolite-mediated longevity and is a hypothesis for future testing, as running the TCA cycle in the reverse of its normal direction was shown to be needed for malate and fumarate-mediated lifespan extension [53].

Glycolysis as a lifespan shortening metabolic pathway in C. elegans

Since supplementation with glucose and other glycolytic precursors decrease lifespan in C. elegans as shown here and in [66,67], there are likely specific metabolic pathways such as glycolysis that decrease lifespan. We propose that many of the supplemented metabolites that increased lifespan are catabolized by mitochondria to increase TCA cycle metabolite levels. The DAF-16/FOXO longevity pathway has been shown to be activated by increased TCA cycle metabolite levels [53]. So the TCA cycle appears to be lifespan-extending metabolic pathway in C. elegans. In addition increased TCA cycle flux could also transiently increase mitochondrial ETC ROS production to activate the SKN-1 longevity pathway as previously suggested [26]. This metabolite oxidation for energy production would also decrease reliance on lifespan-shortening glycolysis as a source of mitochondrial respiratory substrates.

Refinements in C. elegans culture media for lifespan experiments by limiting peptone levels and using heat-killed bacteria during adulthood

When performing lifespan experiments, sources of stress should be removed from the environment, so control animal lifespan is not limited. Unfortunately when working with C. elegans, this has proven difficult due to the slight toxicity of their live E. coli food source. We and others [55] have also found that the peptone present in nematode growth media (NGM) also induces a type of stress that decreases lifespan. It is unclear which component of peptone decreases lifespan as it contains not only proteolyzed proteins (amino acids and oligopeptides), but also fats, metals, salts, vitamins, and other compounds. Because of the slight toxicity associated with the use of peptone and live E. coli, we chose to perform C. elegans lifespan experiments using heat-killed E. coli in liquid S-medium, which lacks peptone. Due to partial degradation of one or more nutrients in the E. coli food source needed for larval development during the heat-killing treatment, it may be advantageous, especially in certain mutant backgrounds, to treat the worms with live E. coli during larval development to ensure adequate nutrition, and then switch them to heat-killed E. coli during adulthood to prevent the bacteria from metabolizing added nutrients. Further refinements in experimental methods will allow C. elegans to become an even more valuable model for investigating the effects of altered metabolism on lifespan.

Conclusions

Individual amino acid supplementation increased the lifespan of C. elegans and increased stress resistance with serine, proline, and tryptophan showing the greatest effects. Many longevity pathways including DAF-16, SKN-1, AAK-2, SIR-2.1, GCN-2, heat shock, autophagy, DR, and inhibition of TOR signaling are involved in these protective effects. Anaplerosis and altered mitochondrial metabolism transiently increasing ROS production to activate SKN-1 appear to be involved in the longevity signaling. The exact pathways involved vary slightly from one amino acid to the next. For example, serine and histidine stimulated transcriptional activity of HIF-1, while 6 other amino acids did not. Likewise 8 lifespan-extending amino acids increased the transcriptional activity of SKN-1, but not tryptophan, cysteine, or the lifespan-decreasing amino acids phenylalanine and asparagine. Uniquely, tryptophan activated the ER stress response and mitochondrial unfolded protein response pathways and lifespan extension was independent of SKN-1 and DAF-16. Future experiments will aim to develop an improved axenic medium that can be used to determine the effects of amino acid restriction on the lifespan of C. elegans. Through the use of both amino acid supplementation and restriction, a diet may one day be developed that can substantially increase stress resistance and slow aging and the onset of aging-associated disorders.

Methods

C. elegans strains and maintenance

C. elegans strains were purchased from the Caenorhabditis Genetics Center (CGC, University of Minnesota) and were cultured in most experiments using standard C. elegans conditions at 20°C in liquid S medium, but in some experiments where indicated standard NGM agar media was used as in [81]. Lifespan assays were performed using the standard C. elegans N2 Bristol strain unless otherwise noted. Lifespan assays were also performed using the following strains: GR1307 [daf-16(mgDf50)], TG38 [aak-2(gt33)], DA1116 [eat-2(ad1116)], VC199 [sir-2.1(ok434)], RB1206 [rsks-1(ok1255)], RB967 [gcn-2(ok871)], RB579 [Ife-2(ok306)], TK22 [mev-1(kn1)], and CW152 [gas-1(fc21)]. Promoter::GFP gene expression reporter experiments were performed with the following strains: SJ4100 [hsp-6::gfp], SJ4058 [hsp-60::gfp], SJ4005 [hsp-4::gfp], CL2070 [hsp-16-2::gfp + pRF4], CL2166[gst-4p::GFP::NLS], ZG449[egl-9(ia61) + nhr-57p::GFP + unc-119(+)], CF1553[sod-3p::GFP + rol-6], and OP37[unc-119(ed3) + pha-4::TY1::EGFP::3xFLAG + unc-119(+)]. Disease and proteostasis protection assays were performed using the following strains: NL5901 [(unc-54p::alpha-synuclein::YFP + unc-119(+))], CL4176 [smg-1ts [myo-3::Aβ1–42 long 3’-UTR]], CL6049 [(snb-1::hTDP-43 + mtl-2::GFP], and AM140 [unc-54p::Q35::YFP].

Chemicals

L-Amino acids were purchased from Acros Organics and Research Products International Corp. Glycine was obtained from Fischer Chemical Company. D-amino acids were purchased from P212121, LLC. When no D or L isomer indication is present before the name of the amino acid (except for glycine), the L isomer was used. 5-fluoro-2’-deoxyuridine (FUdR) was purchased from Research Products International Corp. and Biotang, Inc. Sodium hydroxide (Fischer Scientific) was added to metabolite stock solutions to obtain a pH of 7.0.

Lifespan analysis

Gravid C. elegans adults were bleach treated as previously described [53] to yield age-synchronized eggs. Almost all lifespan experiments were performed using liquid S-medium. Eggs suspended in S-media were placed in 3 μM transparent cell culture inserts (BD Falcon #353181) in 12-well microplates as first described in [82]. HT115 (DE3) E. coli were grown for 20 hours in 2 L flasks with LB media. The E. coli were then spun down, the supernatant poured off, and the pellet was frozen until use. The E. coli were de-thawed and heat-killed at 80°C for 1 hour with slight vibration using a Kendal model HB-S-23DHT ultrasonic cleaner. The E. coli pellets were then resuspended in an equal volume of S-medium. A 1.3 mL suspension of S-medium containing 9 × 109 HT115 (DE3) E. coli per mL was placed in each well of a 12-well microplate. Bleach synchronized worm eggs were suspended at a concentration of 100–200 eggs/mL in the suspension of E. coli in S-medium. Lastly, a cell culture insert was placed in each well followed by 0.25 mL of the egg/bacterial suspension (25–50 eggs) into each insert (n = 3 wells per condition). Synchronized cultures of worms were placed on an orbital shaker at 135 rotations per minute at 20°C and monitored until they reached adulthood (~72 h), at which time FUdR was added to a final concentration of 400 uM. Worm viability was scored every two days. Worms that did not respond to repeated stimulus were scored as dead and those that contained internally hatched larvae were excluded. The culture media containing E. coli in the 12-well plates below each culture insert (>80% of total culture media volume) was changed every 3 days. Lifespan analysis using the CL6049 [snb-1::hTDP-43 + mtl-2::gfp] strain was performed in the same manner except worm viability was counted every day.

High glucose lifespan assays

We performed C. elegans lifespan assays as described above with the addition of 50 mM glucose to the culture medium. Worms were scored for viability every day. The culture media in the 12-well plates was changed every two days.

RNAi feeding experiments

The E. coli skn-1 and bec-1 RNAi clones from the Ahringer C. elegans RNAi library (Source BioScience LifeSciences) were grown 16 hours and then 1 mM IPTG was administered to the E. coli for the last 4 hours of growth to induce expression of the double strand RNA. Lifespan experiments were performed using live instead of heat-killed bacteria. The culture media in the 12-well plates was changed daily instead of every 3 days to decrease the chance of E. coli metabolism depleting the culture level of the supplemented amino acid.

GFP reporter strains

GFP fluorescence of C. elegans populations was assayed using a Biotek Synergy 2 multi-mode microplate reader. Strains were age synchronized and cultured in 12-well microplates as described above. At the L3 stage of larval development, worms were treated with amino acids or other metabolites. Following 24 hours of treatment, worms were washed 3 times in S-medium and approximately 400 worms in 200 μL were added to each well of a clear, flat-bottom 96-well plate, and GFP fluorescence was measured using 485/20 nm excitation and 528/20 nm emission filters (a minimum of n = 8 per treatment group).

Microscopy and quantification

Worms used for microscopy were anesthetized using 1 mM levamisole and transferred to agar pads with glass coverslips and analyzed using an EVOS fluorescence microscope. Comparable results were established in the absence of levamisole. Approximately 20 worms per condition were used and all experiments were repeated at least three times. ImageJ™ software was used to quantify pixel intensities.

Thermotolerance assays

A synchronized population of N2 C. elegans eggs were placed on treated or non-treated NGM agar plates and allowed to hatch at 20°C. At the L4 stage of development animals were transferred to a 35°C incubator. Survival was scored as the number of worms responsive to gentle prodding with a worm pick.

Aß-mediated paralysis assays

Paralysis assays were carried out as outlined in [63]. Briefly, second generation synchronized gravid C. elegans strain CL4176 grown at 16°C were placed on treated or untreated 6 cm NGM agar plates and allowed to lay eggs for 2 hours. After that, adults were removed and plates were placed in a 16°C incubator for 48 hours. Then plates were transferred to a 25°C incubator. Scoring for paralyzed worms began 20 hours after temperature upshift. Animals were scored for movement every two hours. Worms were considered paralyzed if they could not complete a full body movement after stimulation with a worm pick.

Alpha-synuclein aggregation assays

Eggs were collected from the NL5901 strain of C. elegans following treatment with alkaline bleach and placed in 12 well cell culture inserts as described above, with or without amino acid treatment. Following 2 days of treatment, 400 μM FUdR was added to the inserts to prevent progeny. On day 8 worms were washed 3 times with M9 media and either placed on 1% agarose pads to slow movement or immobilized with 1 mM levamisole. Quantification of the number of inclusions expressing alpha-synuclein-YFP was measured using an EVOS fluorescence microscope. Foci larger than 2 μm2 were counted for each group (n = 30). Image analysis was performed using ImageJ™ software and the assay was completed at least 3 times [83]. Statistical analysis was completed using GraphPad Prism software and calculation of statistical significance between groups was carried out using Student’s t-test.

Polyglutamine aggregation assays

AM140 [unc-54p::Q35::YFP] worms were synchronized and placed onto NGM agar plates supplemented with either 1 mM tryptophan, 10 mM serine, or 5 mM proline. Plates were seeded with 90% heat-killed OP50 E. coli and 10% live OP50 E. coli. Images were taken at day 3 of adulthood. Progeny were avoided by picking daily after day 1. Aggregates were scored for 50 worms per condition in independent biological duplicates.

Medium oxygen measurements

Medium oxygen measurements were acquired using flat bottom 96-well PreSens OxoPlates according to the manufacturer’s guidelines. Worm eggs from bleach-killed populations were placed in 12-well cell culture plates in 1 mL of S-medium with live HT115 (DE3) bacteria and a supplemented amino acid. At the L4 developmental stage, worms were washed 3 times with S-media and concentrated to approximately 10 worms/μL. 200 μL of each treatment group was placed into each well of an OxoPlate in replicates of 3–4. Oxygen concentration was measured using an excitation filter of 540/25 nm and emission filters of 590/20 nm (indicator) and 620/40 nm (reference) using a Biotek Synergy 2 microplate reader. Oxygen measurements were normalized to worm protein as in [53].

ATP measurements

Bleach synchronized eggs were grown in liquid S medium in the absence or presence of an amino acid in the presence of live HT115(DE3) E. coli. At the L4 stage of larval development the worms were washed 3 times with S-medium to free them of bacteria and then lysed by repeated freeze-thaw as in [53]. ATP levels were measured using CellTiter-Glo (Promega) according to the manufsacturer’s directions and normalized to worm protein.

Statistical analysis

Kaplan-Meier survival analysis and log-rank tests were performed using Sigmaplot version 11.0. Student’s t-tests were used in other analyses.

Declarations

Acknowledgements

We would like to thank Robert Buzzeo for sharing equipment and reagents. C. elegans strains were obtained from the Caenorhabditis Genetics Center (University of Minnesota, Minneapolis, MN, USA), which is funded by NIH Office of Research Infrastructure Programs (P40 OD010440). The research was funded by NIH grant # AG046769 awarded to PB.

Authors’ Affiliations

(1)
Department of Cell Biology, Microbiology and Molecular Biology, University of South Florida

References

  1. Swire J, Fuchs S, Bundy JG, Leroi AM. The cellular geometry of growth drives the amino acid economy of Caenorhabditis elegans. Proc Biol Sci. 2009;276(1668):2747–54.View ArticlePubMed CentralPubMedGoogle Scholar
  2. Fuchs S, Bundy JG, Davies SK, Viney JM, Swire JS, Leroi AM. A metabolic signature of long life in Caenorhabditis elegans. BMC Biol. 2010;8:14.View ArticlePubMed CentralPubMedGoogle Scholar
  3. Roth E, Druml W. Plasma amino acid imbalance: dangerous in chronic diseases? Curr Opin Clin Nutr Metab Care. 2011;14(1):67–74.View ArticlePubMedGoogle Scholar
  4. Batch BC, Hyland K, Svetkey LP. Branch chain amino acids: biomarkers of health and disease. Curr Opin Clin Nutr Metab Care. 2014;17(1):86–9.PubMedGoogle Scholar
  5. Sohal RS, Weindruch R. Oxidative stress, caloric restriction, and aging. Science. 1996;273(5271):59–63.View ArticlePubMed CentralPubMedGoogle Scholar
  6. Pamplona R, Barja G. Mitochondrial oxidative stress, aging and caloric restriction: the protein and methionine connection. Biochim Biophys Acta. 2006;1757(5–6):496–508.View ArticlePubMedGoogle Scholar
  7. Miller RA, Buehner G, Chang Y, Harper JM, Sigler R, Smith-Wheelock M. Methionine-deficient diet extends mouse lifespan, slows immune and lens aging, alters glucose, T4, IGF-I and insulin levels, and increases hepatocyte MIF levels and stress resistance. Aging Cell. 2005;4(3):119–25.View ArticlePubMedGoogle Scholar
  8. Orentreich N, Matias JR, DeFelice A, Zimmerman JA. Low methionine ingestion by rats extends life span. J Nutr. 1993;123(2):269–74.PubMedGoogle Scholar
  9. Ooka H, Segall PE, Timiras PS. Histology and survival in age-delayed low-tryptophan-fed rats. Mech Ageing Dev. 1988;43(1):79–98.View ArticlePubMedGoogle Scholar
  10. Segall PE, Timiras PS. Patho-physiologic findings after chronic tryptophan deficiency in rats: a model for delayed growth and aging. Mech Ageing Dev. 1976;5(2):109–24.View ArticlePubMedGoogle Scholar
  11. Alvers AL, Fishwick LK, Wood MS, Hu D, Chung HS, Dunn Jr WA, et al. Autophagy and amino acid homeostasis are required for chronological longevity in Saccharomyces cerevisiae. Aging Cell. 2009;8(4):353–69.View ArticlePubMed CentralPubMedGoogle Scholar
  12. Wu Z, Song L, Liu SQ, Huang D. Independent and additive effects of glutamic acid and methionine on yeast longevity. PLoS One. 2013;8(11):e79319.View ArticlePubMed CentralPubMedGoogle Scholar
  13. Kamei Y, Tamura T, Yoshida R, Ohta S, Fukusaki E, Mukai Y. GABA metabolism pathway genes, UGA1 and GAD1, regulate replicative lifespan in Saccharomyces cerevisiae. Biochem Biophys Res Commun. 2011;407(1):185–90.View ArticlePubMedGoogle Scholar
  14. Mirisola MG, Taormina G, Fabrizio P, Wei M, Hu J, Longo VD. Serine- and Threonine/Valine-Dependent Activation of PDK and Tor Orthologs Converge on Sch9 to Promote Aging. PLoS Genet. 2014;10(2):e1004113.View ArticlePubMed CentralPubMedGoogle Scholar
  15. Powers 3rd RW, Kaeberlein M, Caldwell SD, Kennedy BK, Fields S. Extension of chronological life span in yeast by decreased TOR pathway signaling. Genes Dev. 2006;20(2):174–84.View ArticlePubMed CentralPubMedGoogle Scholar
  16. Yoshida R, Tamura T, Takaoka C, Harada K, Kobayashi A, Mukai Y, et al. Metabolomics-based systematic prediction of yeast lifespan and its application for semi-rational screening of ageing-related mutants. Aging Cell. 2010;9(4):616–25.View ArticlePubMedGoogle Scholar
  17. Min KJ, Tatar M. Restriction of amino acids extends lifespan in Drosophila melanogaster. Mech Ageing Dev. 2006;127(7):643–6.View ArticlePubMedGoogle Scholar
  18. Grandison RC, Piper MD, Partridge L. Amino-acid imbalance explains extension of lifespan by dietary restriction in Drosophila. Nature. 2009;462(7276):1061–4.View ArticlePubMed CentralPubMedGoogle Scholar
  19. Kabil H, Kabil O, Banerjee R, Harshman LG, Pletcher SD. Increased transsulfuration mediates longevity and dietary restriction in Drosophila. Proc Natl Acad Sci U S A. 2011;108(40):16831–6.View ArticlePubMed CentralPubMedGoogle Scholar
  20. Ban H, Shigemitsu K, Yamatsuji T, Haisa M, Nakajo T, Takaoka M, et al. Arginine and Leucine regulate p70 S6 kinase and 4E-BP1 in intestinal epithelial cells. Int J Mol Med. 2004;13(4):537–43.PubMedGoogle Scholar
  21. Hara K, Yonezawa K, Weng QP, Kozlowski MT, Belham C, Avruch J. Amino acid sufficiency and mTOR regulate p70 S6 kinase and eIF-4E BP1 through a common effector mechanism. J Biol Chem. 1998;273(23):14484–94.View ArticlePubMedGoogle Scholar
  22. Moskalev AA, Shaposhnikov MV. Pharmacological inhibition of phosphoinositide 3 and TOR kinases improves survival of Drosophila melanogaster. Rejuvenation Res. 2010;13(2–3):246–7.View ArticlePubMedGoogle Scholar
  23. Kapahi P, Zid BM, Harper T, Koslover D, Sapin V, Benzer S. Regulation of lifespan in Drosophila by modulation of genes in the TOR signaling pathway. Curr Biol. 2004;14(10):885–90.View ArticlePubMed CentralPubMedGoogle Scholar
  24. Massie H, Williams T. Effect of sulfur-containing compounds on the life span of Drosophila. Age. 1985;8(4):128–35.View ArticleGoogle Scholar
  25. Zajitschek F, Zajitschek SR, Friberg U, Maklakov AA. Interactive effects of sex, social environment, dietary restriction, and methionine on survival and reproduction in fruit flies. Age (Dordr). 2013;35(4):1193–204.View ArticleGoogle Scholar
  26. Zarse K, Schmeisser S, Groth M, Priebe S, Beuster G, Kuhlow D, et al. Impaired insulin/IGF1 signaling extends life span by promoting mitochondrial L-proline catabolism to induce a transient ROS signal. Cell Metab. 2012;15(4):451–65.View ArticlePubMedGoogle Scholar
  27. van der Goot AT, Zhu W, Vazquez-Manrique RP, Seinstra RI, Dettmer K, Michels H, et al. Delaying aging and the aging-associated decline in protein homeostasis by inhibition of tryptophan degradation. Proc Natl Acad Sci U S A. 2012;109(37):14912–7.View ArticlePubMed CentralPubMedGoogle Scholar
  28. He C, Tsuchiyama SK, Nguyen QT, Plyusnina EN, Terrill SR, Sahibzada S, et al. Enhanced Longevity by Ibuprofen, Conserved in Multiple Species, Occurs in Yeast through Inhibition of Tryptophan Import. PLoS Genet. 2014;10(12):e1004860.View ArticlePubMed CentralPubMedGoogle Scholar
  29. Ferguson AA, Roy S, Kormanik KN, Kim Y, Dumas KJ, Ritov VB, et al. TATN-1 mutations reveal a novel role for tyrosine as a metabolic signal that influences developmental decisions and longevity in Caenorhabditis elegans. PLoS Genet. 2013;9(12):e1004020.View ArticlePubMed CentralPubMedGoogle Scholar
  30. D’Antona G, Ragni M, Cardile A, Tedesco L, Dossena M, Bruttini F, et al. Branched-chain amino acid supplementation promotes survival and supports cardiac and skeletal muscle mitochondrial biogenesis in middle-aged mice. Cell Metab. 2010;12(4):362–72.View ArticlePubMedGoogle Scholar
  31. De Haes W, Frooninckx L, Van Assche R, Smolders A, Depuydt G, Billen J, et al. Metformin promotes lifespan through mitohormesis via the peroxiredoxin PRDX-2. Proc Natl Acad Sci U S A. 2014;111(24):E2501–2509.View ArticlePubMed CentralPubMedGoogle Scholar
  32. Newgard CB. Interplay between lipids and branched-chain amino acids in development of insulin resistance. Cell Metab. 2012;15(5):606–14.View ArticlePubMed CentralPubMedGoogle Scholar
  33. Baker BM, Nargund AM, Sun T, Haynes CM. Protective coupling of mitochondrial function and protein synthesis via the eIF2alpha kinase GCN-2. PLoS Genet. 2012;8(6):e1002760.View ArticlePubMed CentralPubMedGoogle Scholar
  34. Rousakis A, Vlassis A, Vlanti A, Patera S, Thireos G, Syntichaki P. The general control nonderepressible-2 kinase mediates stress response and longevity induced by target of rapamycin inactivation in Caenorhabditis elegans. Aging Cell. 2013;12(5):742–51.View ArticlePubMed CentralPubMedGoogle Scholar
  35. Shibamura A, Ikeda T, Nishikawa Y. A method for oral administration of hydrophilic substances to Caenorhabditis elegans: Effects of oral supplementation with antioxidants on the nematode lifespan. Mech Ageing Dev. 2009;130(9):652–5.View ArticlePubMedGoogle Scholar
  36. Saitoh Y, Katane M, Kawata T, Maeda K, Sekine M, Furuchi T, et al. Spatiotemporal localization of D-amino acid oxidase and D-aspartate oxidases during development in Caenorhabditis elegans. Mol Cell Biol. 2012;32(10):1967–83.View ArticlePubMed CentralPubMedGoogle Scholar
  37. Hamase K, Konno R, Morikawa A, Zaitsu K. Sensitive determination of D-amino acids in mammals and the effect of D-amino-acid oxidase activity on their amounts. Biol Pharm Bull. 2005;28(9):1578–84.View ArticlePubMedGoogle Scholar
  38. Murphy CT, Hu PJ. Insulin/insulin-like growth factor signaling in C. elegans. WormBook 2013:1–43.Google Scholar
  39. Zhang Y, Shao Z, Zhai Z, Shen C, Powell-Coffman JA. The HIF-1 hypoxia-inducible factor modulates lifespan in C. elegans. PLoS One. 2009;4(7):e6348.View ArticlePubMed CentralPubMedGoogle Scholar
  40. Salminen A, Kaarniranta K. AMP-activated protein kinase (AMPK) controls the aging process via an integrated signaling network. Ageing Res Rev. 2012;11(2):230–41.View ArticlePubMedGoogle Scholar
  41. Jia K, Levine B. Autophagy is required for dietary restriction-mediated life span extension in C. elegans. Autophagy. 2007;3(6):597–9.View ArticlePubMedGoogle Scholar
  42. Hansen M, Chandra A, Mitic LL, Onken B, Driscoll M, Kenyon C. A role for autophagy in the extension of lifespan by dietary restriction in C. elegans. PLoS Genet. 2008;4(2):e24.View ArticlePubMed CentralPubMedGoogle Scholar
  43. Panowski SH, Wolff S, Aguilaniu H, Durieux J, Dillin A. PHA-4/Foxa mediates diet-restriction-induced longevity of C. elegans. Nature. 2007;447(7144):550–5.View ArticlePubMedGoogle Scholar
  44. Zhong M, Niu W, Lu ZJ, Sarov M, Murray JI, Janette J, et al. Genome-wide identification of binding sites defines distinct functions for Caenorhabditis elegans PHA-4/FOXA in development and environmental response. PLoS Genet. 2010;6(2):e1000848.View ArticlePubMed CentralPubMedGoogle Scholar
  45. Kim SG, Buel GR, Blenis J. Nutrient regulation of the mTOR complex 1 signaling pathway. Mol Cells. 2013;35(6):463–73.View ArticlePubMed CentralPubMedGoogle Scholar
  46. Robida-Stubbs S, Glover-Cutter K, Lamming DW, Mizunuma M, Narasimhan SD, Neumann-Haefelin E, et al. TOR signaling and rapamycin influence longevity by regulating SKN-1/Nrf and DAF-16/FoxO. Cell Metab. 2012;15(5):713–24.View ArticlePubMed CentralPubMedGoogle Scholar
  47. Vellai T, Takacs-Vellai K, Zhang Y, Kovacs AL, Orosz L, Muller F. Genetics: influence of TOR kinase on lifespan in C. elegans. Nature. 2003;426(6967):620.View ArticlePubMedGoogle Scholar
  48. Chin RM, Fu X, Pai MY, Vergnes L, Hwang H, Deng G et al.. The metabolite alpha-ketoglutarate extends lifespan by inhibiting ATP synthase and TOR. Nature 2014.Google Scholar
  49. Hansen M, Taubert S, Crawford D, Libina N, Lee SJ, Kenyon C. Lifespan extension by conditions that inhibit translation in Caenorhabditis elegans. Aging Cell. 2007;6(1):95–110.View ArticlePubMedGoogle Scholar
  50. Syntichaki P, Troulinaki K, Tavernarakis N. eIF4E function in somatic cells modulates ageing in Caenorhabditis elegans. Nature. 2007;445(7130):922–6.View ArticlePubMedGoogle Scholar
  51. Mouchiroud L, Molin L, Kasturi P, Triba MN, Dumas ME, Wilson MC, et al. Pyruvate imbalance mediates metabolic reprogramming and mimics lifespan extension by dietary restriction in Caenorhabditis elegans. Aging Cell. 2011;10(1):39–54.View ArticlePubMedGoogle Scholar
  52. Chuang M-H, Chiou S-H, Huang C-H, Yang W-B, Wong C-H. The lifespan-promoting effect of acetic acid and Reishi polysaccharide. Bioorg Med Chem. 2009;17(22):7831–40.View ArticlePubMedGoogle Scholar
  53. Edwards CB, Copes N, Brito AG, Canfield J, Bradshaw PC. Malate and fumarate extend lifespan in Caenorhabditis elegans. PLoS One. 2013;8(3):e58345.View ArticlePubMed CentralPubMedGoogle Scholar
  54. Williams DS, Cash A, Hamadani L, Diemer T. Oxaloacetate supplementation increases lifespan in Caenorhabditis elegans through an AMPK/FOXO-dependent pathway. Aging Cell. 2009;8(6):765–8.View ArticlePubMed CentralPubMedGoogle Scholar
  55. Yamaguchi T, Onodera A, Yasuda K, Nishio Y, Arai M, Tsuda M, et al. A low cost and quick assay system using the free-living nematode Caenorhabditis elegans to determine the effects of Kampo medicines on life span. AATEX. 2008;13:1–10.Google Scholar
  56. Hajdu-Cronin YM, Chen WJ, Sternberg PW. The L-type cyclin CYL-1 and the heat-shock-factor HSF-1 are required for heat-shock-induced protein expression in Caenorhabditis elegans. Genetics. 2004;168(4):1937–49.View ArticlePubMed CentralPubMedGoogle Scholar
  57. Kapulkin WJ, Hiester BG, Link CD. Compensatory regulation among ER chaperones in C. elegans. FEBS Lett. 2005;579(14):3063–8.View ArticlePubMedGoogle Scholar
  58. Bennett CF, Kaeberlein M. The mitochondrial unfolded protein response and increased longevity: cause, consequence, or correlation? Exp Gerontol. 2014;56:142–6.View ArticlePubMedGoogle Scholar
  59. Grant RS, Coggan SE, Smythe GA. The physiological action of picolinic acid in the human brain. Int J Tryptophan Res. 2009;2:71–9.PubMed CentralPubMedGoogle Scholar
  60. Lugo-Huitron R, Ugalde Muniz P, Pineda B, Pedraza-Chaverri J, Rios C, Perez-de la Cruz V. Quinolinic acid: an endogenous neurotoxin with multiple targets. Oxid Med Cell Longev. 2013;2013:104024.PubMed CentralPubMedGoogle Scholar
  61. Mouchiroud L, Houtkooper RH, Moullan N, Katsyuba E, Ryu D, Canto C, et al. The NAD(+)/Sirtuin Pathway Modulates Longevity through Activation of Mitochondrial UPR and FOXO Signaling. Cell. 2013;154(2):430–41.View ArticlePubMed CentralPubMedGoogle Scholar
  62. Hayat S, Hayat Q, Alyemeni MN, Wani AS, Pichtel J, Ahmad A. Role of proline under changing environments: a review. Plant Signal Behav. 2012;7(11):1456–66.View ArticlePubMed CentralPubMedGoogle Scholar
  63. Dostal V, Link CD. Assaying beta-amyloid toxicity using a transgenic C. elegans model. J Vis Exp. 2010;44:e2252.Google Scholar
  64. Morley JF, Brignull HR, Weyers JJ, Morimoto RI. The threshold for polyglutamine-expansion protein aggregation and cellular toxicity is dynamic and influenced by aging in Caenorhabditis elegans. Proc Natl Acad Sci U S A. 2002;99(16):10417–22.View ArticlePubMed CentralPubMedGoogle Scholar
  65. Ari C, Poff AM, Held HE, Landon CS, Goldhagen CR, Mavromates N, et al. Metabolic therapy with Deanna Protocol supplementation delays disease progression and extends survival in amyotrophic lateral sclerosis (ALS) mouse model. PLoS One. 2014;9(7):e103526.View ArticlePubMed CentralPubMedGoogle Scholar
  66. Lee S-J, Murphy CT, Kenyon C. Glucose Shortens the Life Span of C. elegans by Downregulating DAF-16/FOXO Activity and Aquaporin Gene Expression. Cell Metab. 2009;10(5):379–91.View ArticlePubMed CentralPubMedGoogle Scholar
  67. Schulz TJ, Zarse K, Voigt A, Urban N, Birringer M, Ristow M. Glucose restriction extends Caenorhabditis elegans life span by inducing mitochondrial respiration and increasing oxidative stress. Cell Metab. 2007;6(4):280–93.View ArticlePubMedGoogle Scholar
  68. Plaisance EP, Greenway FL, Boudreau A, Hill KL, Johnson WD, Krajcik RA, et al. Dietary methionine restriction increases fat oxidation in obese adults with metabolic syndrome. J Clin Endocrinol Metab. 2011;96(5):E836–40.View ArticlePubMed CentralPubMedGoogle Scholar
  69. Massie HR, Aiello VR. The effect of dietary methionine on the copper content of tissues and survival of young and old mice. Exp Gerontol. 1984;19(6):393–9.View ArticlePubMedGoogle Scholar
  70. Depuydt G, Xie F, Petyuk VA, Shanmugam N, Smolders A, Dhondt I, et al. Reduced insulin/insulin-like growth factor-1 signaling and dietary restriction inhibit translation but preserve muscle mass in Caenorhabditis elegans. Mol Cell Proteomics. 2013;12(12):3624–39.View ArticlePubMed CentralPubMedGoogle Scholar
  71. Houtkooper RH, Mouchiroud L, Ryu D, Moullan N, Katsyuba E, Knott G, et al. Mitonuclear protein imbalance as a conserved longevity mechanism. Nature. 2013;497(7450):451–7.View ArticlePubMedGoogle Scholar
  72. Wijeyesekera A, Selman C, Barton RH, Holmes E, Nicholson JK, Withers DJ. Metabotyping of long-lived mice using 1H NMR spectroscopy. J Proteome Res. 2012;11(4):2224–35.View ArticlePubMedGoogle Scholar
  73. Gomes AP, Price NL, Ling AJ, Moslehi JJ, Montgomery MK, Rajman L, et al. Declining NAD(+) induces a pseudohypoxic state disrupting nuclear-mitochondrial communication during aging. Cell. 2013;155(7):1624–38.View ArticlePubMed CentralPubMedGoogle Scholar
  74. Golubnitschaja O, Yeghiazaryan K. Opinion controversy to chromium picolinate therapy’s safety and efficacy: ignoring ‘anecdotes’ of case reports or recognising individual risks and new guidelines urgency to introduce innovation by predictive diagnostics? Epma J. 2012;3(1):11.View ArticlePubMed CentralPubMedGoogle Scholar
  75. Tullet JM, Hertweck M, An JH, Baker J, Hwang JY, Liu S, et al. Direct inhibition of the longevity-promoting factor SKN-1 by insulin-like signaling in C. elegans. Cell. 2008;132(6):1025–38.View ArticlePubMed CentralPubMedGoogle Scholar
  76. Han S, Brunet A. Histone methylation makes its mark on longevity. Trends Cell Biol. 2012;22(1):42–9.View ArticlePubMed CentralPubMedGoogle Scholar
  77. Hamilton B, Dong Y, Shindo M, Liu W, Odell I, Ruvkun G, et al. A systematic RNAi screen for longevity genes in C. elegans. Genes Dev. 2005;19(13):1544–55.View ArticlePubMed CentralPubMedGoogle Scholar
  78. Hashimoto T, Horikawa M, Nomura T, Sakamoto K. Nicotinamide adenine dinucleotide extends the lifespan of Caenorhabditis elegans mediated by sir-2.1 and daf-16. Biogerontology. 2010;11(1):31–43.View ArticlePubMedGoogle Scholar
  79. Marino G, Pietrocola F, Eisenberg T, Kong Y, Malik SA, Andryushkova A, et al. Regulation of autophagy by cytosolic acetyl-coenzyme a. Mol Cell. 2014;53(5):710–25.View ArticlePubMedGoogle Scholar
  80. Mullen AR, Wheaton WW, Jin ES, Chen PH, Sullivan LB, Cheng T, et al. Reductive carboxylation supports growth in tumour cells with defective mitochondria. Nature. 2012;481(7381):385–8.Google Scholar
  81. Stiernagle T. Maintenance of C. elegans. WormBook. 2006;11:1–11.Google Scholar
  82. Fitzgerald VK, Mensack MM, Wolfe P, Thompson HJ. A transfer-less, multi-well liquid culture feeding system for screening small molecules that affect the longevity of Caenorhabditis elegans. Biotechniques. 2009;47(4 Suppl):ix–xv.View ArticlePubMedGoogle Scholar
  83. Shukla V, Phulara SC, Yadav D, Tiwari S, Kaur S, Gupta MM, et al. Iridoid compound 10-O-trans-p-coumaroylcatalpol extends longevity and reduces alpha synuclein aggregation in Caenorhabditis elegans. CNS Neurol Disord Drug Targets. 2012;11(8):984–92.View ArticlePubMedGoogle Scholar

Copyright

© Edwards et al.; licensee BioMed Central. 2015

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Advertisement