Literature DB >> 7535272

A unique subset of rat and human intestinal villus cells express the cystic fibrosis transmembrane conductance regulator.

N A Ameen1, T Ardito, M Kashgarian, C R Marino.   

Abstract

BACKGROUND/AIMS: In the intestine, the cystic fibrosis transmembrane conductance regulator (CFTR) has been localized to the apical pole of crypt epithelial cells. Recent data indicate that some villus cells may also express CFTR, although the identity of these cells has not been established. The aim of the current study was to characterize the distribution, morphology, and surface marker expression of CFTR-expressing villus cells.
METHODS: Immunofluorescence and immunoelectron microscopy was performed using anti-CFTR and enzyme marker antibodies.
RESULTS: In the rat and human proximal small intestine, a subpopulation of scattered villus and superficial crypt epithelial cells label brightly with anti-CFTR antibodies. The fluorescent signal is detected throughout the cells with its greatest concentration apically. At the ultrastructural level, labeling involves the brush border and a prominent subapical vesicular compartment. The cells resemble adjacent villus enterocytes in their abundance of mitochondria and expression of basolateral Na(+)-K(+)-adenosine triphosphatase yet differ in their absence of brush-border sucrase and lactase expression.
CONCLUSIONS: A previously uncharacterized subpopulation of villus cells with high levels of intracellular CFTR expression exists in the proximal small intestine. Morphological and cytochemical studies suggest that this subset of villus cells has a unique transport function.

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Year:  1995        PMID: 7535272     DOI: 10.1016/0016-5085(95)90198-1

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  29 in total

Review 1.  Intestinal ion transport and the pathophysiology of diarrhea.

Authors:  Michael Field
Journal:  J Clin Invest       Date:  2003-04       Impact factor: 14.808

2.  Functional Cftr in crypt epithelium of organotypic enteroid cultures from murine small intestine.

Authors:  Jinghua Liu; Nancy M Walker; Matthew T Cook; Akifumi Ootani; Lane L Clarke
Journal:  Am J Physiol Cell Physiol       Date:  2012-03-07       Impact factor: 4.249

3.  Abnormal passive chloride absorption in cystic fibrosis jejunum functionally opposes the classic chloride secretory defect.

Authors:  Michael A Russo; Christoph Hogenauer; Stephen W Coates; Carol A Santa Ana; Jack L Porter; Randall L Rosenblatt; Michael Emmett; John S Fordtran
Journal:  J Clin Invest       Date:  2003-07       Impact factor: 14.808

4.  Physiological relevance of cell-specific distribution patterns of CFTR, NKCC1, NBCe1, and NHE3 along the crypt-villus axis in the intestine.

Authors:  Robert L Jakab; Anne M Collaco; Nadia A Ameen
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2010-10-28       Impact factor: 4.052

5.  Loss of MYO5B Leads to Reductions in Na+ Absorption With Maintenance of CFTR-Dependent Cl- Secretion in Enterocytes.

Authors:  Amy C Engevik; Izumi Kaji; Melinda A Engevik; Anne R Meyer; Victoria G Weis; Anna Goldstein; Michael W Hess; Thomas Müller; Hermann Koepsell; Pradeep K Dudeja; Matthew Tyska; Lukas A Huber; Mitchell D Shub; Nadia Ameen; James R Goldenring
Journal:  Gastroenterology       Date:  2018-08-23       Impact factor: 22.682

6.  A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.

Authors:  P J French; J H van Doorninck; R H Peters; E Verbeek; N A Ameen; C R Marino; H R de Jonge; J Bijman; B J Scholte
Journal:  J Clin Invest       Date:  1996-09-15       Impact factor: 14.808

7.  Vimentin-positive cells in the epithelium of rabbit ileal villi represent cup cells but not M-cells.

Authors:  Carolina Ramirez; Andreas Gebert
Journal:  J Histochem Cytochem       Date:  2003-11       Impact factor: 2.479

8.  Characterization of CFTR High Expresser cells in the intestine.

Authors:  Robert L Jakab; Anne M Collaco; Nadia A Ameen
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2013-07-18       Impact factor: 4.052

9.  Assessment of cystic fibrosis transmembrane conductance regulator (CFTR) activity in CFTR-null mice after bone marrow transplantation.

Authors:  Emanuela M Bruscia; Joanna E Price; Ee-Chun Cheng; Scott Weiner; Christina Caputo; Elisa C Ferreira; Marie E Egan; Diane S Krause
Journal:  Proc Natl Acad Sci U S A       Date:  2006-02-15       Impact factor: 11.205

10.  Polarization of specific tropomyosin isoforms in gastrointestinal epithelial cells and their impact on CFTR at the apical surface.

Authors:  Jacqueline Rae Dalby-Payne; Edward Vincent O'Loughlin; Peter Gunning
Journal:  Mol Biol Cell       Date:  2003-09-05       Impact factor: 4.138

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