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通过Rap1信号传导控制细胞粘附动力学。

Control of cell adhesion dynamics by Rap1 signaling.

作者信息

Boettner Benjamin, Van Aelst Linda

机构信息

Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.

出版信息

Curr Opin Cell Biol. 2009 Oct;21(5):684-93. doi: 10.1016/j.ceb.2009.06.004. Epub 2009 Jul 16.

Abstract

Individual cells in their particular environments adhere to the extracellular matrix (ECM) and their neighbours via integrin-containing and cadherin-containing complexes, respectively. The dynamics of these interactions regulate the formation and maintenance of complex tissues. An expanding body of evidence accentuates the role of the small Rap1 GTPase and its associated signaling network in many of these processes. In this review we will discuss more recently revealed roles of Rap1 signaling by primarily focusing on functions of the Rap1 effectors RIAM, KRIT-1/CCM1 and AF-6/Afadin in junctional regulation of the vascular system and in epithelial cells. Furthermore, we will describe novel findings on the Rap activator PDZ-GEF in the regulation of cell-cell adhesion between epithelial cells and within a stem cell niche.

摘要

单个细胞在其特定环境中,分别通过含整合素的复合物和含钙黏蛋白的复合物与细胞外基质(ECM)及其相邻细胞黏附。这些相互作用的动态过程调节着复杂组织的形成和维持。越来越多的证据凸显了小Rap1 GTP酶及其相关信号网络在许多此类过程中的作用。在本综述中,我们将主要聚焦于Rap1效应子RIAM、KRIT-1/CCM1和AF-6/Afadin在血管系统和上皮细胞连接调节中的功能,来讨论Rap1信号最近揭示的作用。此外,我们将描述Rap激活剂PDZ-GEF在上皮细胞间以及干细胞龛内细胞-细胞黏附调节方面的新发现。

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