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Regulation of RhoA Activity by Adhesion Molecules and Mechanotransduction

机译:黏附分子和机械转导调节RhoA活性

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摘要

The low molecular weight GTP-binding protein RhoA regulates many cellular events, including cell migration, organization of the cytoskeleton, cell adhesion, progress through the cell cycle and gene expression. Physical forces influence these cellular processes in part by regulating RhoA activity through mechanotransduction of cell adhesion molecules (e.g. integrins, cadherins, Ig superfamily molecules). RhoA activity is regulated by guanine nucleotide exchange factors (GEFs) and GTPase activating proteins (GAPs) that are themselves regulated by many different signaling pathways. Significantly, the engagement of many cell adhesion molecules can affect RhoA activity in both positive and negative ways. In this brief review, we consider how RhoA activity is regulated downstream from cell adhesion molecules and mechanical force. Finally, we highlight the importance of mechanotransduction signaling to RhoA in normal cell biology as well as in certain pathological states.
机译:低分子量GTP结合蛋白RhoA调节许多细胞事件,包括细胞迁移,细胞骨架组织,细胞粘附,细胞周期进展和基因表达。物理力通过调节细胞粘附分子(例如整联蛋白,钙黏着蛋白,Ig超家族分子)的RhoA活性来部分影响这些细胞过程。 RhoA活性受鸟嘌呤核苷酸交换因子(GEFs)和GTPase活化蛋白(GAPs)调节,而鸟嘌呤核苷酸交换因子和GTPase活化蛋白(GAPs)本身也受许多不同的信号传导途径调节。重要的是,许多细胞粘附分子的参与可以正向和负向两种方式影响RhoA活性。在这篇简短的综述中,我们考虑了如何在细胞粘附分子和机械力下游调节RhoA活性。最后,我们强调了在正常细胞生物学以及某些病理状态下机械转导RhoA信号的重要性。

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