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Wound-induced contractile ring: a model for cytokinesis.

机译:伤口引起的收缩环:胞质分裂的模型。

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摘要

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.
机译:基于肌动蛋白的收缩环是多种生物学过程所必需的,例如伤口愈合和动物细胞的胞质分裂。尽管在定义这种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放线菌素环是如何在空间和时间上组装的,我们也不了解其收缩的分子机制。最近的结果表明F-肌动蛋白和肌球蛋白-II的微管依赖局部组装存在于伤口闭合中,并且与动物细胞的胞质分裂相似。此外,在两个过程中,信号因子(例如小的Rho GTPases)均已显示出对肌动蛋白动力学的调节。在这篇综述中,我们着眼于最近的发现,试图更好地了解与动物细胞分裂的最终步骤相比,在伤口愈合过程中肌动球蛋白收缩环的动力学。

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