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RhoA和ROCK通过限制膜突出促进迁移。

RhoA and ROCK promote migration by limiting membrane protrusions.

作者信息

Worthylake Rebecca A, Burridge Keith

机构信息

Department of Cell and Developmental Biology, Lineberger Comprehensive Cancer Center and Comprehensive Center for Inflammatory Disorders, University of North Carolina, Chapel Hill, North Carolina 27599, USA.

出版信息

J Biol Chem. 2003 Apr 11;278(15):13578-84. doi: 10.1074/jbc.M211584200. Epub 2003 Feb 6.

Abstract

Previously, we and others have shown that RhoA and ROCK signaling are required for negatively regulating integrin-mediated adhesion and for tail retraction of migrating leukocytes. This study continues our investigation into the molecular mechanisms underlying RhoA/ROCK-regulated integrin adhesion. We show that inhibition of ROCK up-regulates integrin-mediated adhesion, which is accompanied by both increased phosphotyrosine signaling through Pyk-2 and paxillin and inappropriate membrane protrusions. We provide evidence that inhibition of ROCK induces integrin adhesion by promoting remodeling of the actin cytoskeleton. Furthermore, we find that ROCK regulates membrane activity through a pathway involving cofilin. Inhibition of RhoA signaling allows the formation of multiple competing lamellipodia that disrupt productive migration of monocytes. Together, our results show that RhoA/ROCK signaling promotes migration by restricting integrin activity and membrane protrusions to the leading edge.

摘要

此前,我们和其他研究人员已表明,RhoA和ROCK信号传导对于负向调节整合素介导的黏附以及迁移白细胞的尾部回缩是必需的。本研究继续探讨RhoA/ROCK调节整合素黏附的分子机制。我们发现,抑制ROCK会上调整合素介导的黏附,这伴随着通过Pyk-2和桩蛋白增加的磷酸酪氨酸信号传导以及不适当的膜突出。我们提供的证据表明,抑制ROCK通过促进肌动蛋白细胞骨架的重塑来诱导整合素黏附。此外,我们发现ROCK通过涉及丝切蛋白的途径调节膜活性。抑制RhoA信号传导会导致形成多个相互竞争的片状伪足,从而破坏单核细胞的有效迁移。总之,我们的结果表明,RhoA/ROCK信号传导通过将整合素活性和膜突出限制在前缘来促进迁移。

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