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Rho A and Rac1: Antagonists moving forward

机译:rho a和rac1:敌人前进

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Cells detect external stimuli through cell-surface receptors. In cases where the stimulus is a cytokine or a growth factor, the cell responds by inducing modifications in the actin cytoskeleton. These changes are mediated through the Rho family of GTPases. Among these GTPases, RhoA, Rac1 and Cdc42 have been extensively studied. The activity of these proteins is closely monitored and tightly regulated through Guanine-nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs) that turn the "switch" on and off respectively. Crosstalk between Rho GTPases has been long studied; yet many questions are raised regarding the spatio-temporal regulation of these GTPases, particularly RhoA and Rac1. This review sheds a light on the antagonistic relationship between both GTPases and puts emphasis on the importance of cycling of RhoA activation at the focal adhesions for optimal cell migration.
机译:细胞通过细胞表面受体检测外部刺激。 在刺激是细胞因子或生长因子的情况下,细胞通过在肌动蛋白细胞骨架中诱导修饰来响应。 这些变化通过GTP酶的Rho系列介导。 在这些GTP酶中,RHOA,RAC1和CDC42已被广泛研究。 这些蛋白质的活性受到通过鸟嘌呤 - 核苷酸交换因子(GEF)和GTP酶活化蛋白(间隙)分别切开和关闭的GTP酶活性蛋白质(GTP酶活化蛋白质(间隙)紧密调节。 rho gtpases之间的串扰已经长期研究; 还提出了许多问题,关于这些GTP酶的时空调节,特别是RHOA和RAC1。 这篇评论阐明了GTP酶之间的拮抗关系,并强调循环激活在局灶性粘连中的循环激活的重要性,以实现最佳细胞迁移。

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