Ladwein Markus, Rottner Klemens
Cytoskeleton Dynamics Group, Helmholtz Centre for Infection Research (HZI), Inhoffen Strasse 7, D-38124 Braunschweig, Germany.
FEBS Lett. 2008 Jun 18;582(14):2066-74. doi: 10.1016/j.febslet.2008.04.033. Epub 2008 Apr 28.
Cell migration entails the formation of cellular protrusions such as lamellipodia or filopodia, the growth of which is powered by the polymerisation of actin filaments abutting the plasma membrane. Specific Rho-GTPase subfamilies are able to drive different types of protrusions. However, significant crosstalk between Rho-family members and the interplay of distinct Rho-effectors regulating or modulating actin reorganization in protrusions complicate the picture of how precisely they are initiated and maintained. Here, we briefly sketch our current knowledge on structure and dynamics of different protrusions as well as their regulation by Rho-GTPases. We also comment on topical, unresolved controversies in the field, with special emphasis on the interrelation of different protrusion types, and on the composition of the nanomachineries driving them.
细胞迁移需要形成诸如片状伪足或丝状伪足等细胞突起,其生长由紧邻质膜的肌动蛋白丝聚合提供动力。特定的Rho-GTPase亚家族能够驱动不同类型的突起。然而,Rho家族成员之间存在显著的相互作用,以及不同的Rho效应器在突起中调节或调控肌动蛋白重组的相互作用,使得它们如何精确启动和维持的情况变得复杂。在这里,我们简要概述了我们目前对不同突起的结构和动力学及其由Rho-GTPases调控的了解。我们还评论了该领域当前未解决的争议话题,特别强调了不同突起类型之间的相互关系以及驱动它们的纳米机器的组成。