O'Connor Kathleen, Chen Min
University of Kentucky; Lexington, KY.
Small GTPases. 2013 Jul-Sep;4(3):141-7. doi: 10.4161/sgtp.25131. Epub 2013 Jun 10.
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 migration has 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 stress fiber generation to permit RhoA-mediated lamellae formation.
RhoA是小GTP酶Rho家族中研究较为广泛的成员之一,它最显著的作用是对肌动蛋白-肌球蛋白收缩性和应力纤维形成的贡献。因此,RhoA在细胞迁移过程中的功能被认为主要在细胞后部,介导后缘的回缩。然而,RhoA也能介导膜褶皱、片状伪足形成和膜泡形成,这表明它在前沿膜突出中发挥积极作用。随着基于荧光共振能量转移(FRET)的Rho活性报告基因的出现,研究表明RhoA在迁移细胞的前沿具有活性,且早于Rac和Cdc42的激活。这些观察结果证明了RhoA信号传导具有显著的多功能性,但RhoA功能如何在收缩和突出之间切换仍是一个谜。本综述重点介绍了关于Rho效应蛋白Rhotekin和S100A4的合作如何抑制应力纤维生成以允许RhoA介导片状伪足形成的最新进展。