缺氧与肌动蛋白细胞骨架的调节——新兴的相互关系

A. Zieseniss
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引用次数: 45

摘要

最近对缺氧对细胞功能影响的研究进展揭示了肌动蛋白细胞骨架与缺氧之间相互关系的新信息;不过,细节仍不明朗。缺氧时肌动蛋白细胞骨架的动态调控是复杂的,在不同的细胞和组织中是不同的,也取决于缺氧的方式。一些分子参与者和途径正在出现,有助于调节肌动蛋白细胞骨架,并影响缺氧时肌动蛋白结合蛋白的大量曲目。本文介绍并讨论了在缺氧条件下肌动蛋白细胞骨架动力学方面积累的知识,特别强调了Rho家族的小鸟苷三磷酸酶(Rho GTPases)。鉴于RhoA, Rac和Cdc42已经被很好地表征,本文将重点关注这些Rho GTPases家族成员。值得注意的是,在一些细胞类型和组织中,缺氧可能通过Rho GTPase信号传导,诱导肌动蛋白重排和肌动蛋白应激纤维组装,这是缺氧时肌动蛋白细胞骨架的普遍调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypoxia and the modulation of the actin cytoskeleton – emerging interrelations
Recent progress in understanding the influence of hypoxia on cell function has revealed new information about the interrelationship between the actin cytoskeleton and hypoxia; nevertheless, details remain cloudy. The dynamic regulation of the actin cytoskeleton during hypoxia is complex, varies in different cells and tissues, and also depends on the mode of hypoxia. Several molecular players and pathways are emerging that contribute to the modulation of the actin cytoskeleton and that affect the large repertoire of actin-binding proteins in hypoxia. This review describes and discusses the accumulated knowledge about actin cytoskeleton dynamics in hypoxia, placing special emphasis on the Rho family of small guanosine triphosphatases (Rho GTPases). Given that RhoA, Rac and Cdc42 are very well characterized, the review is focused on these family members of Rho GTPases. Notably, in several cell types and tissues, hypoxia, presumably via Rho GTPase signaling, induces actin rearrangement and actin stress fiber assembly, which is a prevalent modulation of the actin cytoskeleton in hypoxia.
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