Format

Send to

Choose Destination
See comment in PubMed Commons below
J Clin Invest. 2010 Sep;120(9):3093-6. doi: 10.1172/JCI44235. Epub 2010 Aug 25.

Transgenic animals may help resolve a sticky situation in cystic fibrosis.

Author information

1
Department of Physiology and Membrane Biology, University of California Davis, Davis, California 95616-8664, USA. jhwiddicombe@ucdavis.edu

Abstract

Cystic fibrosis (CF) is caused by defects in the CFTR, a cAMP-activated Cl- channel of epithelia. The resulting reduction in epithelial fluid transport creates abnormally viscous secretions from airway mucous glands that may be a major factor in CF pathology. Mouse airways have few mucous glands, and the mouse model of CF exhibits no significant airway disease. Pigs and ferrets, however, have approximately the same number of airway mucous glands as humans. In this issue of the JCI, three independent research groups conclude that changes in airway mucous gland function in CFTR-deficient animals of these species resemble the changes seen in human CF. It is expected, therefore, that these animals will develop lung disease similar to human CF and prove to be valuable models on which to test potential therapies.

PMID:
20739746
PMCID:
PMC2929743
DOI:
10.1172/JCI44235
[Indexed for MEDLINE]
Free PMC Article
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for American Society for Clinical Investigation Icon for PubMed Central
    Loading ...
    Support Center