Suarez Cristian, Kovar David R
Department of Molecular Genetics and Cell Biology, The University of Chicago.
Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, Illinois 60637, USA.
Nat Rev Mol Cell Biol. 2016 Dec;17(12):799-810. doi: 10.1038/nrm.2016.106. Epub 2016 Sep 14.
Cells precisely control the formation of dynamic actin cytoskeleton networks to coordinate fundamental processes, including motility, division, endocytosis and polarization. To support these functions, actin filament networks must be assembled, maintained and disassembled at the correct time and place, and with proper filament organization and dynamics. Regulation of the extent of filament network assembly and of filament network organization has been largely attributed to the coordinated activation of actin assembly factors through signalling cascades. Here, we discuss an intriguing model in which actin monomer availability is limiting and competition between homeostatic actin cytoskeletal networks for actin monomers is an additional crucial regulatory mechanism that influences the density and size of different actin networks, thereby contributing to the organization of the cellular actin cytoskeleton.
细胞精确控制动态肌动蛋白细胞骨架网络的形成,以协调包括运动、分裂、内吞作用和极化在内的基本过程。为支持这些功能,肌动蛋白丝网络必须在正确的时间和地点进行组装、维持和解聚,并具有适当的丝组织和动力学。丝状网络组装程度和丝状网络组织的调节在很大程度上归因于通过信号级联对肌动蛋白组装因子的协同激活。在这里,我们讨论一个有趣的模型,其中肌动蛋白单体的可用性是有限的,稳态肌动蛋白细胞骨架网络之间对肌动蛋白单体的竞争是另一种关键的调节机制,它影响不同肌动蛋白网络的密度和大小,从而有助于细胞肌动蛋白细胞骨架的组织。