Rapid disruption of intestinal barrier function by gliadin involves altered expression of apical junctional proteins.

Abstract:

:Coeliac disease is a chronic enteropathy caused by the ingestion of wheat gliadin and other cereal prolamines derived from rye and barley. In the present work, we investigated the mechanisms underlying altered barrier function properties exerted by gliadin-derived peptides in human Caco-2 intestinal epithelial cells. We demonstrate that gliadin alters barrier function almost immediately by decreasing transepithelial resistance and increasing permeability to small molecules (4 kDa). Gliadin caused a reorganisation of actin filaments and altered expression of the tight junction proteins occludin, claudin-3 and claudin-4, the TJ-associated protein ZO-1 and the adherens junction protein E-cadherin.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Sander GR,Cummins AG,Henshall T,Powell BC

doi

10.1016/j.febslet.2005.07.066

keywords:

subject

Has Abstract

pub_date

2005-08-29 00:00:00

pages

4851-5

issue

21

eissn

0014-5793

issn

1873-3468

pii

S0014-5793(05)00929-4

journal_volume

579

pub_type

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