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伤口诱导收缩环:一种胞质分裂模型。

Wound-induced contractile ring: a model for cytokinesis.

作者信息

Darenfed Hassina, Mandato Craig A

机构信息

Department of Anatomy and Cell Biology, Mc Gill University, Montreal, QC, Canada.

出版信息

Biochem Cell Biol. 2005 Dec;83(6):711-20. doi: 10.1139/o05-164.

Abstract

The actomyosin-based contractile ring is required for several biological processes, such as wound healing and cytokinesis of animal cells. Despite progress in defining the roles of this structure in both wound closure and cell division, we still do not fully understand how an actomyosin ring is spatially and temporally assembled, nor do we understand the molecular mechanism of its contraction. Recent results have demonstrated that microtubule-dependent local assembly of F-actin and myosin-II is present in wound closure and is similar to that in cytokinesis in animal cells. Furthermore, signalling factors such as small Rho GTPases have been shown to be involved in the regulation of actin dynamics during both processes. In this review we address recent findings in an attempt to better understand the dynamics of actomyosin contractile rings during wound healing as compared with the final step of animal cell division.

摘要

基于肌动球蛋白的收缩环参与多种生物学过程,如动物细胞的伤口愈合和胞质分裂。尽管在确定该结构在伤口闭合和细胞分裂中的作用方面取得了进展,但我们仍不完全了解肌动球蛋白环是如何在空间和时间上组装的,也不了解其收缩的分子机制。最近的研究结果表明,依赖微管的F-肌动蛋白和肌球蛋白-II局部组装存在于伤口闭合过程中,并且与动物细胞胞质分裂中的情况相似。此外,诸如小Rho GTP酶等信号因子已被证明在这两个过程中参与肌动蛋白动力学的调节。在这篇综述中,我们阐述了最近的研究发现,以期更好地理解伤口愈合过程中肌动球蛋白收缩环的动态变化,并与动物细胞分裂的最后阶段进行比较。

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