Intestinal barrier dysfunction triggered by invasive bacteria

被引:85
作者
Barreau, F. [1 ,2 ,3 ,4 ]
Hugot, J. P. [1 ,2 ,3 ,5 ]
机构
[1] Univ Paris Diderot, Sorbonne Paris Cite, UMR 843, F-75018 Paris, France
[2] INSERM, UMR 843, F-75018 Paris, France
[3] Labex Inflamex, F-75018 Paris, France
[4] Univ Toulouse, INSERM, Ctr Physiopathol Toulouse, UMR 1043, Toulouse, France
[5] Hop Robert Debre, AP HP, F-75019 Paris, France
关键词
LIGHT-CHAIN KINASE; EPITHELIAL TIGHT JUNCTIONS; ADHESION PROTEIN LAP; DIFFICILE TOXIN-A; ESCHERICHIA-COLI; LISTERIA-MONOCYTOGENES; PARACELLULAR TRANSLOCATION; SALMONELLA-ENTERICA; SHIGELLA-FLEXNERI; INTERFERON-GAMMA;
D O I
10.1016/j.mib.2013.12.003
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
The ability to control uptake across the mucosa and to protect the gut from harmful substances present in the lumen is defined as intestinal barrier function. Two routes are usually distinguished for transepithelial transport. The paracellular route allows the passage of ions and small molecules and is mainly regulated by tight junctions (TJ). The transcellular route concerns large molecules or small particles (including bacteria) and is mediated by cell endocytosis and intracellular vesicular traffic. Enteropathogenic bacteria increase the transcellular permeability, especially in the follicle-associated epithelium. They also modulate TJ opening via the redistribution of TJ proteins and the activation of the myosin light chain kinase (MLCK). This review focuses on the molecular mechanisms involved in the bacteria-induced barrier defect and briefly discusses their consequences in human diseases.
引用
收藏
页码:91 / 98
页数:8
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