| First Author | Kent G | Year | 1996 |
| Journal | Pediatr Res | Volume | 40 |
| Issue | 2 | Pages | 233-41 |
| PubMed ID | 8827771 | Mgi Jnum | J:35002 |
| Mgi Id | MGI:82454 | Doi | 10.1203/00006450-199608000-00008 |
| Citation | Kent G, et al. (1996) Phenotypic abnormalities in long-term surviving cystic fibrosis mice. Pediatr Res 40(2):233-41 |
| abstractText | Mouse models for cystic fibrosis (CF) with no CFTR function (Cftr-/-) have the disadvantage that most animals die of intestinal obstruction shortly after weaning. The objective of this research was to extend the lifespan of CF mice and characterize their phenotype. Weanlings were placed on a nutrient liquid diet, and histologic and functional aspects of organs implicated in the disease were subsequently examined. Approximately 90% of Cftr-/- mice survived to 60 d, the majority beyond 100 d. Cftr-/- mice were underweight and had markedly abnormal intestinal histology. The intestinal epithelia did not respond to challenges with agents that raised intracellular cAMP, consistent with the absence of functional CFTR. No lesions or functional abnormalities were evident in the lungs. Liquid-fed Cftr-/- mice were infertile, although some males weaned to a solid diet were fertile before they died. Thus, we have succeeded in using dietary means to prolong the lives of Cftr-/- mice. |
