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Regulation of actin dynamics by PI(4,5)P-2 in cell migration and endocytosis

机译:细胞迁移和内吞作用中Pi(4,5)P-2对肌动蛋白动力学的调节

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摘要

The actin cytoskeleton is indispensable for several cellular processes, including migration, morphogenesis, polarized growth, endocytosis, and phagocytosis. The organization and dynamics of the actin cytoskeleton in these processes are regulated by Rho family small GTPases and kinase-phosphatase pathways. Moreover, membrane phospholipids, especially the phosphatidylinositol phosphates have emerged as important regulators of actin dynamics. From these, PI(4,5)P-2 is the most abundant at the plasma membrane, and directly regulates the activities and subcellular localizations of numerous actin-binding proteins. Here, we discuss recent studies demonstrating that actin-binding proteins interact with PI(4,5)P-2-rich membranes through drastically different affinities and dynamics correlating with their roles in cytoskeletal dynamics. Moreover, by using mesenchymal cell migration and clathrin-mediated endocytosis as examples, we present a model for how interplay between PI(4,5)P-2 and actin-binding proteins control the actin cytoskeleton in cells.
机译:肌动蛋白细胞骨架对于几种细胞方法是必不可少的,包括迁移,形态发生,偏振生长,内吞作用和吞噬作用。这些方法中肌动蛋白细胞骨架的组织和动态由RHO家族小GTP酶和激酶 - 磷酸酶途径调节。此外,膜磷脂,尤其是磷脂酰肌醇磷酸盐作为肌动蛋白动态的重要调节剂。由此,PI(4,5)P-2位于血浆膜中最丰富,直接调节众多肌动蛋白结合蛋白的活性和亚细胞局部。在这里,我们讨论最近的研究表明,肌动蛋白结合蛋白通过巨大不同的不同亲和力和动力学与其在细胞骨骼动态中的作用相关性和动态。此外,通过使用间充质细胞迁移和克拉林介导的内吞作用作为实施例,我们介绍了PI(4,5)P-2和肌动蛋白结合蛋白之间的相互作用的模型控制细胞中的肌动蛋白细胞骨架。

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