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RhoG 和 Cdc42 可以通过与 WAVE 调节复合物结合来促进 Rac 依赖性片状伪足的形成。

RhoG and Cdc42 can contribute to Rac-dependent lamellipodia formation through WAVE regulatory complex-binding.

机构信息

Division of Molecular Cell Biology, Zoological Institute, Technische Universität Braunschweig , Braunschweig, Germany.

Cell Biology, Helmholtz Centre for Infection Research , Braunschweig, Germany.

出版信息

Small GTPases. 2021 Mar;12(2):122-132. doi: 10.1080/21541248.2019.1657755. Epub 2019 Aug 26.

Abstract

Cell migration frequently involves the formation of lamellipodial protrusions, the initiation of which requires Rac GTPases signalling to heteropentameric WAVE regulatory complex (WRC). While Rac-related RhoG and Cdc42 can potently stimulate lamellipodium formation, so far presumed to occur by upstream signalling to Rac activation, we show here that the latter can be bypassed by RhoG and Cdc42 given that WRC has been artificially activated. This evidence arises from generation of B16-F1 cells simultaneously lacking both Rac GTPases and WRC, followed by reconstitution of lamellipodia formation with specific Rho-GTPase and differentially active WRC variant combinations. We conclude that formation of canonical lamellipodia requires WRC activation through Rac, but can possibly be tuned, in addition, by WRC interactions with RhoG and Cdc42.

摘要

细胞迁移通常涉及片状伪足的形成,其起始需要 Rac GTPases 信号转导至异源五聚体 WAVE 调节复合物 (WRC)。虽然 Rac 相关的 RhoG 和 Cdc42 可以强烈刺激片状伪足的形成,但迄今为止,据推测是通过上游信号转导到 Rac 激活,但我们在这里表明,只要 WRC 被人为激活,RhoG 和 Cdc42 就可以绕过 Rac。这一证据来自于同时缺乏 Rac GTPases 和 WRC 的 B16-F1 细胞的生成,然后用特定的 Rho-GTPase 和具有不同活性的 WRC 变体组合来重建片状伪足的形成。我们的结论是,典型的片状伪足的形成需要通过 Rac 激活 WRC,但此外,还可以通过 WRC 与 RhoG 和 Cdc42 的相互作用进行调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b0a/7849749/87714f0dc081/KSGT_A_1657755_F0001_OC.jpg

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