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Rho激酶调节紧密连接功能,并且对于极化肠道上皮细胞中紧密连接的组装是必需的。

Rho kinase regulates tight junction function and is necessary for tight junction assembly in polarized intestinal epithelia.

作者信息

Walsh S V, Hopkins A M, Chen J, Narumiya S, Parkos C A, Nusrat A

机构信息

Epithelial Pathobiology Research Unit, Department of Pathology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

出版信息

Gastroenterology. 2001 Sep;121(3):566-79. doi: 10.1053/gast.2001.27060.

Abstract

BACKGROUND & AIMS: Tight junctions are crucial determinants of barrier function in polarized intestinal epithelia and are regulated by Rho guanosine triphosphatase. Rho kinase (ROCK) is a downstream effector of Rho.

METHODS

A specific inhibitor of ROCK, Y-27632, was used to examine the role of ROCK in the regulation of tight junctions in model intestinal (T84) cells by electrophysiologic, biochemical, morphologic, and molecular biologic approaches.

RESULTS

ROCK inhibition induced reorganization of apical F-actin structures and enhanced paracellular permeability but did not alter the distribution or detergent solubility of tight junction proteins. Confocal microscopy showed colocalization of a subpool of ROCK with the tight junction protein zonula occludens 1. Inhibition of ROCK function by a dominant negative mutant of ROCK also produced reorganization of apical F-actin structures without disruption of tight junctions. ROCK inhibition in calcium switch assays showed that ROCK is necessary for the assembly of tight and adherens junctions. Upon calcium repletion, occludin, zonula occludens 1, and E-cadherin failed to redistribute to the intercellular junctions; assembly of the apical F-actin cytoskeleton was prevented; and barrier function failed to recover.

CONCLUSIONS

We suggest that ROCK regulates intact tight junctions via its effects on the F-actin cytoskeleton. ROCK is also critical for assembly of the apical junctional proteins and the F-actin cytoskeleton organization during junctional formation.

摘要

背景与目的

紧密连接是极化肠上皮细胞屏障功能的关键决定因素,受 Rho 鸟苷三磷酸酶调控。Rho 激酶(ROCK)是 Rho 的下游效应器。

方法

使用 ROCK 的特异性抑制剂 Y-27632,通过电生理、生化、形态学和分子生物学方法,研究 ROCK 在模型肠(T84)细胞紧密连接调控中的作用。

结果

ROCK 抑制诱导顶端 F-肌动蛋白结构重组并增强细胞旁通透性,但未改变紧密连接蛋白的分布或去污剂溶解性。共聚焦显微镜显示 ROCK 的一个亚群与紧密连接蛋白闭合蛋白 1 共定位。用 ROCK 的显性负性突变体抑制 ROCK 功能也会导致顶端 F-肌动蛋白结构重组,而不破坏紧密连接。在钙转换实验中抑制 ROCK 表明,ROCK 是紧密连接和黏附连接组装所必需的。钙补充后,闭合蛋白、闭合蛋白 1 和 E-钙黏蛋白未能重新分布到细胞间连接;顶端 F-肌动蛋白细胞骨架的组装被阻止;屏障功能未能恢复。

结论

我们认为,ROCK 通过对 F-肌动蛋白细胞骨架的作用来调节完整的紧密连接。ROCK 在连接形成过程中对顶端连接蛋白的组装和 F-肌动蛋白细胞骨架组织也至关重要。

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