Das Mitali, Ithychanda Sujay, Qin Jun, Plow Edward F
Department of Molecular Cardiology, Joseph J. Jacobs Center for Thrombosis and Vascular Biology, Lerner Research Institute, Cleveland Clinic.
Biochim Biophys Acta. 2014 Feb;1838(2):579-88. doi: 10.1016/j.bbamem.2013.07.017. Epub 2013 Jul 24.
Cells undergo dynamic remodeling of the cytoskeleton during adhesion and migration on various extracellular matrix (ECM) substrates in response to physiological and pathological cues. The major mediators of such cellular responses are the heterodimeric adhesion receptors, the integrins. Extracellular or intracellular signals emanating from different signaling cascades cause inside-out signaling of integrins via talin, a cystokeletal protein that links integrins to the actin cytoskeleton. Various integrin subfamilies communicate with each other and growth factor receptors under diverse cellular contexts to facilitate or inhibit various integrin-mediated functions. Since talin is an essential mediator of integrin activation, much of the integrin crosstalk would therefore be influenced by talin. However, despite the existence of an extensive body of knowledge on the role of talin in integrin activation and as a stabilizer of ECM-actin linkage, information on its role in regulating inter-integrin communication is limited. This review will focus on the structure of talin, its regulation of integrin activation and discuss its potential role in integrin crosstalk. This article is part of a Special Issue entitled: Reciprocal influences between cell cytoskeleton and membrane channels, receptors and transporters. Guest Editor: Jean Claude Hervé.
细胞在响应生理和病理信号时,于各种细胞外基质(ECM)底物上进行黏附与迁移的过程中会经历细胞骨架的动态重塑。此类细胞反应的主要介导物是异二聚体黏附受体——整合素。源自不同信号级联反应的细胞外或细胞内信号,通过踝蛋白(一种将整合素与肌动蛋白细胞骨架相连的细胞骨架蛋白)引发整合素的外向内信号传导。在不同的细胞环境下,各种整合素亚家族相互沟通并与生长因子受体相互作用,以促进或抑制各种整合素介导的功能。由于踝蛋白是整合素激活的关键介导物,因此许多整合素间的相互作用会受到踝蛋白的影响。然而,尽管关于踝蛋白在整合素激活以及作为ECM - 肌动蛋白连接稳定剂方面的作用已有大量知识,但关于其在调节整合素间通讯中的作用信息却很有限。本综述将聚焦于踝蛋白的结构、其对整合素激活的调节,并探讨其在整合素相互作用中的潜在作用。本文是名为:细胞骨架与膜通道、受体及转运体之间的相互影响的特刊的一部分。客座编辑:让·克洛德·埃尔韦。