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Dynamic functions of RhoA in tumor cell migration and invasion

机译:RhoA在肿瘤细胞迁移和侵袭中的动态功能

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摘要

RhoA is one of the more extensively studied members of the Rho family of small GTPase where it is most readily recognized for its contributions to actin-myosin contractility and stress fiber formation. Accordingly, RhoA function during cell migrationhas been relegated to the rear of the cell where it mediates retraction of the trailing edge. However, RhoA can also mediate membrane ruffling, lamellae formation and membrane blebbing, thus suggesting an active role in membrane protrusions at the leading edge. With the advent of fluorescence resonance energy transfer (FRET)-based Rho activity reporters, RhoA has been shown to be active at the leading edge of migrating cells where it precedes Rac and Cdc42 activation. These observations demonstrate a remarkable versatility to RhoA signaling, but how RhoA function can switch between contraction and protrusion has remained an enigma. This review highlights recent advances regarding how the cooperation of Rho effector Rhotekin and S100A4 suppresses stressfiber generation to permit RhoA-mediated lamellae formation.
机译:RhoA是Rho家族小GTPase家族中研究最广泛的成员之一,在Rho家族中,它对肌动蛋白-肌球蛋白的收缩性和应激纤维形成的贡献最为明显。因此,在细胞迁移过程中,RhoA功能已降级到细胞的后部,在其中它介导后缘的收缩。但是,RhoA也可以介导膜起皱,薄片形成和膜起泡,因此表明在前缘膜突起中起积极作用。随着基于荧光共振能量转移(FRET)的Rho活性报道基因的出现,RhoA已被证明在迁移细胞的前沿具有活性,在Rac和Cdc42激活之前。这些观察结果表明,RhoA信号具有广泛的用途,但是RhoA功能如何在收缩和突出之间转换仍然是一个谜。这篇综述突出了有关Rho效应器Rhotekin和S100A4的合作如何抑制应激纤维生成以允许RhoA介导的薄片形成的最新进展。

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