共 136 条
Cytoskeletal Regulation of Epithelial Barrier Function During Inflammation
被引:309
作者:
Ivanov, Andrei I.
[1
]
Parkos, Charles A.
[2
]
Nusrat, Asma
[2
]
机构:
[1] Univ Rochester, Dept Med, Div Gastroenterol & Hepatol, Med Ctr, Rochester, NY 14642 USA
[2] Emory Univ, Dept Pathol & Lab Med, Epithelial Pathobiol Res Unit, Atlanta, GA 30322 USA
基金:
美国国家卫生研究院;
关键词:
LIGHT-CHAIN KINASE;
APICAL JUNCTIONAL COMPLEX;
DISRUPTS TIGHT JUNCTIONS;
ACTIN-FILAMENT TURNOVER;
NONMUSCLE MYOSIN-II;
CELL-CELL CONTACTS;
BOWEL-DISEASE;
INTESTINAL PERMEABILITY;
CROHNS-DISEASE;
IN-VITRO;
D O I:
10.2353/ajpath.2010.100168
中图分类号:
R36 [病理学];
学科分类号:
100104 ;
摘要:
Increased epithelial permeability is a common and important consequence of mucosal inflammation that results in perturbed body homeostasis and enhanced exposure to external pathogens. The integrity and barrier properties of epithelial layers are regulated by specialized adhesive plasma membrane structures known as intercellular junctions. It is generally believed that inflammatory stimuli increase transepithelial permeability by inducing junctional disassembly. This review highlights molecular events that lead to disruption of epithelial junctions during inflammation. We specifically focus on key mechanisms of junctional regulation that are dependent on reorganization of the perijunctional F-actin cytoskeleton. We discuss critical roles of myosin-II-dependent contractility and actin filament turnover in remodeling of the F-actin cytoskeleton that drive disruption of epithelial barriers under different inflammatory conditions. Finally, we highlight signaling pathways induced by inflammatory mediators that regulate reorganization of actin filaments and junctional disassembly in mucosal epithelia. (Am J Pathol 2010, 177:512-524; DOI: 10.2353/ajpath.2010.100168)
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页码:512 / 524
页数:13
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