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PMID: 11093933 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Molecular physiology and pathophysiology of tight junctions V. assault of the tight junction by enteric pathogens.

American journal of physiology. Gastrointestinal and liver physiology ·Vol. 279 ·No. 6 ·2000-12-00 ·Pages G1129-34

Sears CL

Abstract

Studies of the impact of enteric pathogens and their virulence factors on the proteins comprising the tight junction and zonula adherens offer a novel approach to dissection of tight junctional complex regulation. Most studies to date provide only tantalizing clues that select pathogens may indeed assault the tight junctional complex. Information on critical human pathogens such as Campylobacter jejuni and Shigella and Salmonella subspecies is lacking. Mechanistic studies are currently sparse, but available results on pathogenic Escherichia coli and specific virulence factors such as the Rho-modifying and protease bacterial toxins indicate four major mechanisms by which these pathogens may act: 1) direct cleavage of tight junctional structural proteins; 2) modification of the actin cytoskeleton; 3) activation of cellular signal transduction; and 4) triggering transmigration of polymorphonuclear cells across the epithelial cell barrier. New therapeutics may evolve from detailed studies of these pathogens and the cellular processes and proteins they disrupt.

MeSH Terms
Animals Campylobacter Infections/physiopathology Campylobacter jejuni Enteritis/physiopathology Enterobacteriaceae Infections/physiopathology Humans Intestines/microbiology Tight Junctions/physiology
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Sears C L
Divisions of Infectious Diseases and Gastroenterology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2196, USA. csears@jhmi.edu
Article Info
Journal
American journal of physiology. Gastrointestinal and liver physiology
Abbr.
Am J Physiol Gastrointest Liver Physiol
ISSN
0193-1857
Published
2000-12-00
Pages
G1129-34
Language
English
Region
United States
NLM ID
100901227
Subset
IM
Grants
NIDDK NIH HHS · DK-45496 · United States
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