- Research article
- Open Access
The "Goldilocks Effect" in Cystic Fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse
© Craig Cohen et al; licensee BioMed Central Ltd. 2004
- Received: 18 May 2004
- Accepted: 27 July 2004
- Published: 27 July 2004
Cystic Fibrosis is a pleiotropic disease in humans with primary morbidity and mortality associated with a lung disease phenotype. However, knockout in the mouse of cftr, the gene whose mutant alleles are responsible for cystic fibrosis, has previously failed to produce a readily, quantifiable lung phenotype.
Using measurements of pulmonary mechanics, a definitive lung phenotype was demonstrated in the cftr-/- mouse. Lungs showed decreased compliance and increased airway resistance in young animals as compared to cftr+/+ littermates. These changes were noted in animals less than 60 days old, prior to any long term inflammatory effects that might occur, and are consistent with structural differences in the cftr-/- lungs. Surprisingly, the cftr+/- animals exhibited a lung phenotype distinct from either the homozygous normal or knockout genotypes. The heterozygous mice showed increased lung compliance and decreased airway resistance when compared to either homozygous phenotype, suggesting a heterozygous advantage that might explain the high frequency of this mutation in certain populations.
In the mouse the gene dosage of cftr results in distinct differences in pulmonary mechanics of the adult. Distinct phenotypes were demonstrated in each genotype, cftr-/-, cftr +/-, and cftr+/+. These results are consistent with a developmental role for CFTR in the lung.
- Cystic Fibrosis
- Cystic Fibrosis Transmembrane Conductance Regulator
- Functional Residual Capacity
- Lung Weight
- Peep Level
Cystic fibrosis (CF) is a progressive disease primarily affecting the intestines, lungs, and pancreas. The gene responsible for CF was identified in 1989  as coding for the cystic fibrosis transmembrane conductance regulator (cftr), a membrane chloride channel. CF is one of the most common autosomal recessive diseases in Caucasians with a carrier rate of 3–4% , and is characterized by recurrent infection and chronic inflammation. Recently it was found that infants with CF demonstrate changes in forced expiratory volume in 1 second (FEV1), functional residual capacity (FRC), and other parameters of lung function prior to the onset of recurrent infection [3–5].
Soon after the CF gene was discovered, a knockout mouse was developed. This mouse demonstrates subtle changes in epithelial cell phenotype, including alterations in secretory glycoconjugates and changes in secretory vesicles . Monocytic infiltrates and altered lung mechanics have also been found . Unfortunately, the cftr knockout mouse does not develop overt lung disease, which has severely limited its usefulness. However, the availability of new methods for pulmonary testing in rodents [8, 9] now presents the opportunity to re-examine the cftr knockout mouse for functional lung changes. In the present study, therefore, we examined pulmonary function in young adult cftr -/-, cftr +/-, and cftr+/+ S489x mice in an effort to establish a lung phenotype.
Effect of cftr gene dosage on pressure-volume (PV) curves
The static compliance (Cst) of the lungs, which reflects elastic recoil at a given pressure, was calculated from the slopes of the PV curves. As shown in Figure 1B, the static compliance of the homozygous knockout lung was significantly decreased compared to the homozygous normal lung (p < 0.01)). Furthermore, Cst was significantly reduced in both cftr+/+ (p < 0.001) and cftr-/- (p < 0.001) as compared to age-matched cftr+/- mice. Hysteresis was altered among the 3 genotypes (Figure 1C). A statistically significant increase in hysteresis was observed in both cftr+/- (P < 0.0001) and cftr+/+ mice (p < 0.05) compared to cftr-/- mice. These data suggest the presence of a gene dosage effect in which an altered lung structure in the heterozygous animals leads to an elevated compliance relative to the two homozygous animals. Lung weights were measured and no statistically significant differences were observed among the three genotypes (Figure 1D).
Airway mechanics of cftr deficient lungs
Relative effect of genotype on lung function compared to that observed in the cftr+/+ mouse.
PV curve position
A particularly intriguing further observation was that Cst and hysteresis in cftr+/- mice was significantly higher than in cftr+/+ animals while G and H were decreased. As this was not associated with any pathology such as emphysema, we conclude that it represents a functionally different lung from that of the cftr+/+. Our data thus reveal a remarkable inverse correlation between the effect of one and two non-functional copies of the cftr gene.
What do these data mean in terms of lung structure? The knockout animal has cystic fibrosis by definition, and our data now show it to also have lung disease manifest as a reduced compliance and increased resistance. These changes could reflect changes in the intrinsic mechanical properties of the parenchyma, or simply a reduction in lung volume. The former effect could include alterations in the biophysical properties of the air-liquid interface in the lungs, and would be expected to result in a change in η. Indeed, because cftr is a chloride channel and is thought to be involved in water balance, a change in surface tension in the lung, and consequently in η, might be expected. However, as shown in Figure 2 and Table 1, although G and H both increase, they do so in the same proportion so there is no significant change in η between the three cftr genotypes. On the other hand, lung weights were not different among the different groups of mice, so the decreased compliance and increased resistance of the cftr-/- animals was not simply due to their having smaller lungs than control animals. This suggests that the parenchymal structure in the lungs of the homozygous and heterozygous animals were organized differently, in a manner that affected G and H similarly.
As documented in numerous publications, the mouse strain used in the present study does not develop chronic inflammatory disease up to the age (30–60 days) used in this study (for review see ). On the other hand, Broaches-Carter et al.  have shown that cftr levels are highest in the developing lung and decrease 75-fold at birth. In utero over-expression of cftr has also been shown to affect lung growth and development, and the severity of disease in the knockout mouse has been shown to be influenced by genetic background . These data thus suggest that cftr may affect the early development of the lung in a manner that is affected by the interaction of other genes.
Are there any functional consequences for increased lung compliance in the heterozygous cftr animals? Interestingly, there is no decrement in lung function in human heterozygotes [19–21]. Also, the heterozygote frequency for CF in humans is higher than expected, likely reflecting a selective advantage because there is no evidence for genetic drift [22, 23]. Indeed, selective advantage in CF has been proposed to reflect resistance to tuberculosis, influenza and cholera . When one looks in nature for other examples of heterozygous advantage, the sickle cell trait which confers resistance to malaria  is perhaps the only such recognized genetic trait in humans. In Norway rats, a single Mendelian gene controls resistance to Warfarin, an anticoagulant used to control rat populations; homozygous wild-type rats are killed by Warfarin and homozygous mutant allele animals are highly susceptible to vitamin K deficiency . The results of the present study indicate that a similar selective advantage may pertain to cftr, something we term a "Goldilocks Effect". That is, while two defective copies of the gene are detrimental and two normal copies are satisfactory, one normal and one defective gene may results in an optimal dosage for lung development.
Further studies of pulmonary mechanics in cftr knockout mice should reveal additional genetic loci that modulate the influence of cftr on lung growth and development. Corresponding studies in humans should be useful in evaluating the effect of therapies on reversing altered pulmonary function in the CF patient.
Using sophisticated techniques to a evaluate rodent pulmonary function; a distinct, readily quantifiable lung phenotype was identified in the cftr knockout mouse. In addition, the cftr+/- mouse had a distinguishable pulmonary function phenotype from that observed in either the homozygous normal or mutant genotype mice. These data are consistent with CFTR-dependent, physiologic changes in the structure and function of the lung.
The S489X mouse 5th generation backcross to C57Bl/6 has been maintained by random mating for the past 8 years. This colony has a 100% mortality rate among cftr knockouts by 45 days of age unless the animals are placed on an elemental liquid diet and corncob bedding upon weaning . Mice 30–60 days of age from our S489X mouse colony were genotyped for the normal and mutant cftr alleles. Age and litter matched cftr+/+ and cftr+/- were used for each cftr-/- mouse examined. Six animals were included in each group. All experiments were approved by the animal care and use committee.
Pulmonary function tests
The mice were anesthetized with intra-peritoneal pentobarbital (90 mg/kg) and the trachea was dissected free of surrounding tissue and cannulated with a 20-gauge cannula. The animals were then connected to a small animal ventilator (flexiVent, SCIREQ Inc. Montreal, PQ, Canada) and ventilated with a tidal volume of 10 ml/kg; inspiratory:expiratory ratio of 66.67%, respiratory rate of 150 breaths/minute, and maximum pressure of 30 cmH20. PEEP was controlled by submerging the expiratory limb from the ventilator into a water trap. Each animal was paralyzed with pancuronium bromide (0.5 mg/kg) and allowed to equilibrate on the ventilator until spontaneous breathing ceased (5 minutes).
To measure Zrs, mechanical ventilation was interrupted and the animal was allowed to expire against the set level of PEEP for 1 s. We then applied an 8 s broad-band volume perturbation signal to the lungs with the flexiVent, after which ventilated was resumed. This was repeated at PEEP levels of 0, 3 and 6 cmH2O. The volume perturbation signal consisted of the superposition of 18 sine waves having frequency spaced roughly evenly over the range 0.25 Hz to 19.625 Hz. Zrs was calculated from the displacement of the ventilator's piston and the pressure in its cylinder as described previously [10, 11]. Correction for gas compressibility as well as resistive and accelerative losses in the flexiVent, connecting tubing and the tracheal cannula were performed as described previously  using dynamic calibration data obtained by applying volume perturbations through the tubing and tracheal cannula first when it was completely closed and then when it was open to the atmosphere.
We interpreted the measurement of Zrs in terms of the constant phase model 
where Raw is a frequency independent Newtonian resistance reflecting that of the conducting airways, Iaw is airway gas inertance, G characterizes tissue damping, H characterizes tissue stiffness (elastance), i is the imaginary unit, α links G and H, and f is frequency. We also calculated a quantity known as hysteresivity (η = G/H), which is believed to increase when regional heterogeneities develop in the lung . Raw, G and H were all normalized by multiplication by lung weight.
Starting at the FRC defined by the PEEP, the flexiVent was programmed to deliver seven inspiratory volume steps for a total volume of 0.8 ml followed by seven expiratory steps, pausing at each step for 1 s. Plateau pressure (P) at each step was recorded and related to the total volume (V) delivered to produce a quasi-static PV curve. Cst was calculated from the slope of each curve , and was normalized by division by lung weight.
Zrs measurements at each PEEP level and PV curves were obtained in triplicate. Data were statistically evaluated using paired t-test with p < 0.05 being taken as significant
This work was supported by the Ochsner Clinic Foundation and NIH grants R01 HL-67273 and NCRR COBRE P20 RR-15557. The authors thank Dr. Conrad Hornick for his assistance.
- Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, Zielenski J, Lok S, Plavsic N, Chou JL, et al.: Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989, 245: 1066-1073.View ArticlePubMedGoogle Scholar
- Raman V, Clary R, Siegrist KL, Zehnbauer B, Chatila TA: Increased prevalence of mutations in the cystic fibrosis transmembrane conductance regulator in children with chronic rhinosinusitis. Pediatrics. 2002, 109: E13-View ArticlePubMedGoogle Scholar
- Hart N, Polkey MI, Clement A, Boule M, Moxham J, Lofaso F, Fauroux B: Changes in pulmonary mechanics with increasing disease severity in children and young adults with cystic fibrosis. Am J Respir Crit Care Med. 2002, 166: 61-66. 10.1164/rccm.2112059.View ArticlePubMedGoogle Scholar
- Sharp JK: Monitoring early inflammation in CF. Infant pulmonary function testing. Clin Rev Allergy Immunol. 2002, 23: 59-76. 10.1385/CRIAI:23:1:059.View ArticlePubMedGoogle Scholar
- Tepper RS, Zander JE, Eigen H: Chronic respiratory problems in infancy. Curr Probl Pediatr. 1986, 16: 305-359.PubMedGoogle Scholar
- Cohen JC, Morrow SL, Cork RJ, Delcarpio JB, Larson JE: Molecular pathophysiology of cystic fibrosis based on the rescued knockout mouse model. Mol Genet Metab. 1998, 64: 108-118. 10.1006/mgme.1998.2683.View ArticlePubMedGoogle Scholar
- Kent G, Oliver M, Foskett JK, Frndova H, Durie P, Forstner J, Forstner GG, Riordan JR, Percy D, Buchwald M: Phenotypic abnormalities in long-term surviving cystic fibrosis mice. Pediatr Res. 1996, 40: 233-241.View ArticlePubMedGoogle Scholar
- Allen JT, Spiteri MA: Growth factors in idiopathic pulmonary fibrosis: relative roles. Respir Res. 2002, 3: 13-10.1186/rr162.PubMed CentralView ArticlePubMedGoogle Scholar
- Pillow JJ, Wilkinson MH, Neil HL, Ramsden CA: In vitro performance characteristics of high-frequency oscillatory ventilators. Am J Respir Crit Care Med. 2001, 164: 1019-1024.View ArticlePubMedGoogle Scholar
- Gomes RF, Shen X, Ramchandani R, Tepper RS, Bates JH: Comparative respiratory system mechanics in rodents. J Appl Physiol. 2000, 89: 908-916.PubMedGoogle Scholar
- Hirai T, McKeown KA, Gomes RF, Bates JH: Effects of lung volume on lung and chest wall mechanics in rats. J Appl Physiol. 1999, 86: 16-21.PubMedGoogle Scholar
- Hantos Z, Daroczy B, Suki B, Nagy S, Fredberg JJ: Input impedance and peripheral inhomogeneity of dog lungs. J Appl Physiol. 1992, 72: 168-178. 10.1063/1.352153.View ArticlePubMedGoogle Scholar
- Geiser M, Zimmermann B, Baumann M, Cruz-Orive LM: Does lack of Cftr gene lead to developmental abnormalities in the lung?. Exp Lung Res. 2000, 26: 551-564. 10.1080/019021400750048090.View ArticlePubMedGoogle Scholar
- Fredberg JJ, Stamenovic D: On the imperfect elasticity of lung tissue. J Appl Physiol. 1989, 67: 2408-2419.PubMedGoogle Scholar
- Stotland PK, Radzioch D, Stevenson MM: Mouse models of chronic lung infection with Pseudomonas aeruginosa: models for the study of cystic fibrosis. Pediatr Pulmonol. 2000, 30: 413-424. 10.1002/1099-0496(200011)30:5<413::AID-PPUL8>3.3.CO;2-0.View ArticlePubMedGoogle Scholar
- Broackes-Carter FC, Mouchel N, Gill D, Hyde S, Bassett J, Harris A: Temporal regulation of CFTR expression during ovine lung development: implications for CF gene therapy. Hum Mol Genet. 2002, 11: 125-131. 10.1093/hmg/11.2.125.View ArticlePubMedGoogle Scholar
- Larson JE, Delcarpio JB, Farberman MM, Morrow SL, Cohen JC: CFTR modulates lung secretory cell proliferation and differentiation. Am J Physiol Lung Cell Mol Physiol. 2000, 279: L333-41.PubMedGoogle Scholar
- Haston CK, McKerlie C, Newbigging S, Corey M, Rozmahel R, Tsui LC: Detection of modifier loci influencing the lung phenotype of cystic fibrosis knockout mice. Mamm Genome. 2002, 13: 605-613. 10.1007/s00335-002-2190-7.View ArticlePubMedGoogle Scholar
- Hallett WY, Knudson A. G., Jr., Massey F. J., Jr.: Absence of detrimental effect of the carrier state for the cystic fibrosis gene. Am Rev Respir Dis. 1965, 92: 714-724.PubMedGoogle Scholar
- Byard PJ, Davis PB: Pulmonary function in obligate heterozygotes for cystic fibrosis. Am Rev Respir Dis. 1988, 138: 312-316.View ArticlePubMedGoogle Scholar
- Davis PB, Byard PJ: Heterozygotes for cystic fibrosis: models for study of airway and autonomic reactivity. J Appl Physiol. 1989, 66: 2124-2128.PubMedGoogle Scholar
- Pritchard DJ: Cystic fibrosis allele frequency, sex ratio anomalies and fertility: a new theory for the dissemination of mutant alleles. Hum Genet. 1991, 87: 671-676.View ArticlePubMedGoogle Scholar
- Romeo G, Devoto M, Galietta LJ: Why is the cystic fibrosis gene so frequent?. Hum Genet. 1989, 84: 1-5.View ArticlePubMedGoogle Scholar
- Gabriel SE, Brigman KN, Koller BH, Boucher RC, Stutts MJ: Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model. Science. 1994, 266: 107-109.View ArticlePubMedGoogle Scholar
- Bayoumi RA: The sickle-cell trait modifies the intensity and specificity of the immune response against P. falciparum malaria and leads to acquired protective immunity. Med Hypotheses. 1987, 22: 287-298. 10.1016/0306-9877(87)90193-9.View ArticlePubMedGoogle Scholar
- Greaves JH, Ayres PB: Multiple allelism at the locus controlling warfarin resistance in the Norway rat. Genet Res. 1982, 40: 59-64.View ArticlePubMedGoogle Scholar
- Larson JE, Morrow SL, Happel L, Sharp JF, Cohen JC: Reversal of cystic fibrosis phenotype in mice by gene therapy in utero. Lancet. 1997, 349: 619-620.View ArticlePubMedGoogle Scholar
- Bates JH, Schuessler TF, Dolman C, Eidelman DH: Temporal dynamics of acute isovolume bronchoconstriction in the rat. J Appl Physiol. 1997, 82: 55-62.PubMedGoogle Scholar
- Tomioka S, Bates JH, Irvin CG: Airway and tissue mechanics in a murine model of asthma: alveolar capsule vs. forced oscillations. J Appl Physiol. 2002, 93: 263-270.View ArticlePubMedGoogle Scholar
- Lutchen KR, Hantos Z, Petak F, Adamicza A, Suki B: Airway inhomogeneities contribute to apparent lung tissue mechanics during constriction. J Appl Physiol. 1996, 80: 1841-1849.PubMedGoogle Scholar
- Salazar E, Knowles JH: An Analysis of Pressure-Volume Characteristics of the Lungs. J Appl Physiol. 1964, 19: 97-104.PubMedGoogle Scholar
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