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环状背翅形成的调控机制研究进展。

Mechanistic insights into the regulation of circular dorsal ruffle formation.

机构信息

Division of Membrane Biology, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Kobe 650-0017, Japan.

出版信息

J Biochem. 2013 Jan;153(1):21-9. doi: 10.1093/jb/mvs138. Epub 2012 Nov 21.

Abstract

Growth factor stimulations induce dynamic changes in the cytoskeleton beneath the plasma membrane. Among them is the formation of membrane ruffles organized in a circular array, called 'circular dorsal ruffles' (CDRs). Physiological functions of CDRs include downregulation of cell growth by desensitizing the signalling from growth factor receptors as well as rearrangement of adhesion sites at the onset of cell migration. For the formation of CDRs, not only the activators of actin polymerization, such as N-WASP and the Arp2/3-complex, but also membrane deforming proteins with BAR/F-BAR domains are necessary. Small GTPases are also involved in the formation of CDRs by controlling intracellular trafficking through endosomes. Moreover, recent analyses of another circular cytoskeletal structure, podosome rosettes, have revealed common molecular features shared with CDRs. Among them, the roles of PI3-kinase and phosphoinositide 5-phosphatase may hold the key to the induction of these circular structures.

摘要

生长因子刺激会引起质膜下细胞骨架的动态变化。其中包括以环形方式排列的膜皱襞的形成,称为“环形背侧皱襞”(CDR)。CDR 的生理功能包括通过使生长因子受体信号脱敏来下调细胞生长,以及在细胞迁移开始时重新排列粘附位点。对于 CDR 的形成,不仅需要肌动蛋白聚合的激活剂,如 N-WASP 和 Arp2/3 复合物,还需要具有 BAR/F-BAR 结构域的膜变形蛋白。小 GTPases 也通过控制通过内体的细胞内运输参与 CDR 的形成。此外,对另一种环形细胞骨架结构——微绒毛玫瑰花环的最近分析揭示了与 CDR 共享的共同分子特征。其中,PI3-激酶和磷酸肌醇 5-磷酸酶的作用可能是诱导这些环形结构的关键。

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