Hall A
MRC Laboratory for Molecular Cell Biology and Department of Biochemistry and Molecular Biology, Cancer Research UK Oncogene and Signal Transduction Group, University College London, London WC1E 6BT, UK.
Biochem Soc Trans. 2005 Nov;33(Pt 5):891-5. doi: 10.1042/BST20050891.
Rho, Rac and Cdc42, three members of the Rho family of small GTPases, each control a signal transduction pathway linking membrane receptors to the assembly and disassembly of the actin cytoskeleton and of associated integrin adhesion complexes. Rho regulates stress fibre and focal adhesion assembly, Rac regulates the formation of lamellipodia protrusions and membrane ruffles, and Cdc42 triggers filopodial extensions at the cell periphery. These observations have led to the suggestion that wherever filamentous actin is used to drive a cellular process, Rho GTPases are likely to play an important regulatory role. Rho GTPases have also been reported to control other cellular activities, such as the JNK (c-Jun N-terminal kinase) and p38 MAPK (mitogen-activated protein kinase) cascades, an NADPH oxidase enzyme complex, the transcription factors NF-kappaB (nuclear factor kappaB) and SRF (serum-response factor), and progression through G1 of the cell cycle. Thus Rho, Rac and Cdc42 can regulate the actin cytoskeleton and gene transcription to promote co-ordinated changes in cell behaviour. We have been analysing the biochemical contributions of Rho GTPases in cell movement and have found that Rac controls cell protrusion, while Cdc42 controls cell polarity.
Rho、Rac和Cdc42是小GTP酶Rho家族的三个成员,它们各自控制一条信号转导途径,该途径将膜受体与肌动蛋白细胞骨架及相关整联蛋白黏附复合物的组装和拆卸联系起来。Rho调节应力纤维和黏着斑的组装,Rac调节片状伪足突起和膜皱褶的形成,而Cdc42触发细胞周边丝状伪足的延伸。这些观察结果表明,无论在何处使用丝状肌动蛋白来驱动细胞过程,Rho GTP酶都可能发挥重要的调节作用。据报道,Rho GTP酶还控制其他细胞活动,如JNK(c-Jun氨基末端激酶)和p38 MAPK(丝裂原活化蛋白激酶)级联反应、一种NADPH氧化酶复合物、转录因子NF-κB(核因子κB)和SRF(血清反应因子),以及细胞周期G1期的进程。因此,Rho、Rac和Cdc42可以调节肌动蛋白细胞骨架和基因转录,以促进细胞行为的协调变化。我们一直在分析Rho GTP酶在细胞运动中的生化作用,发现Rac控制细胞突起,而Cdc42控制细胞极性。