Zhang Li, Mao Yuntao S, Janmey Paul A, Yin Helen L
Department of Physiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, 75390-9040, Dallas, TX, USA.
Subcell Biochem. 2012;59:177-215. doi: 10.1007/978-94-007-3015-1_6.
Dynamic changes in PM PIP(2) have been implicated in the regulation of many processes that are dependent on actin polymerization and remodeling. PIP(2) is synthesized primarily by the type I phosphatidylinositol 4 phosphate 5 kinases (PIP5Ks), and there are three major isoforms, called a, b and g. There is emerging evidence that these PIP5Ks have unique as well as overlapping functions. This review will focus on the isoform-specific roles of individual PIP5K as they relate to the regulation of the actin cytoskeleton. We will review recent advances that establish PIP(2) as a critical regulator of actin polymerization and cytoskeleton/membrane linkages, and show how binding of cytoskeletal proteins to membrane PIP(2) might alter lateral or transverse movement of lipids to affect raft formation or lipid asymmetry. The mechanisms for specifying localized increase in PIP(2) to regulate dynamic actin remodeling will also be discussed.
质膜磷脂酰肌醇-4,5-二磷酸(PM PIP(2))的动态变化与许多依赖于肌动蛋白聚合和重塑的过程的调节有关。PIP(2)主要由I型磷脂酰肌醇-4-磷酸-5-激酶(PIP5Ks)合成,有三种主要的亚型,分别称为α、β和γ。越来越多的证据表明,这些PIP5Ks具有独特以及重叠的功能。本综述将聚焦于各个PIP5K亚型特异性的作用,因为它们与肌动蛋白细胞骨架的调节相关。我们将回顾近期的进展,这些进展确立了PIP(2)作为肌动蛋白聚合以及细胞骨架/膜连接的关键调节因子,并展示细胞骨架蛋白与膜PIP(2)的结合如何可能改变脂质的侧向或横向运动,从而影响脂筏形成或脂质不对称性。还将讨论使PIP(2)局部增加以调节动态肌动蛋白重塑的机制。