Non-CFTR chloride channels likely contribute to secretion in the murine small intestine View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2001-11

AUTHORS

Katalin Gyömörey, Elizabeth Garami, Kevin Galley, Johanna M. Rommens, Christine E. Bear

ABSTRACT

While most cystic fibrosis (CF) transmembrane conductance regulator (CFTR)-knockout animals die due to intestinal obstruction before or at the time of weaning, a subpopulation of these animals are long living and exhibit a milder phenotype. The decreased severity of intestinal disease in these mildly affected CF mice is related to the expression of non-CFTR genetic modifiers. The identity of these genetic modifiers is not known, but we hypothesize that they may complement CFTR function as a chloride channel in this tissue. To assess the contribution of non-CFTR chloride channels to chloride secretion across the small intestine of CF mice with mild disease, we measured the basal transepithelial potential difference across this tissue as well as the secretory response to agonists of the cAMP and the calcium-mediated signaling pathways. Chloride secretion across the small intestine of mildly affected CF mice was not stimulated by forskolin or by carbachol. The absence of CFTR is thus not compensated by the activity of a distinct, cAMP- or calcium-activated chloride channel at the apical surface of the intestinal epithelium. On the other hand, a basal chloride secretion across the intestinal epithelium was present in these animals, and we hypothesize that this activity may be linked to improved survival of these animals. More... »

PAGES

s103-s106

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s004240100654

DOI

http://dx.doi.org/10.1007/s004240100654

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1025313350

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/11845313


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