Welch Matthew D, Mullins R Dyche
Department of Molecular and Cell Biology, 301 LSA, University of California, Berkeley 94720-3200, USA.
Annu Rev Cell Dev Biol. 2002;18:247-88. doi: 10.1146/annurev.cellbio.18.040202.112133. Epub 2002 Apr 2.
Eukaryotic cells use actin polymerization to change shape, move, and internalize extracellular materials by phagocytosis and endocytosis, and to form contractile structures. In addition, several pathogens have evolved to use host cell actin assembly for attachment, internalization, and cell-to-cell spread. Although cells possess multiple mechanisms for initiating actin polymerization, attention in the past five years has focused on the regulation of actin nucleation-the formation of new actin filaments from actin monomers. The Arp2/3 complex and the multiple nucleation-promoting factors (NPFs) that regulate its activity comprise the only known cellular actin-nucleating factors and may represent a universal machine, conserved across eukaryotic phyla, that nucleates new actin filaments for various cellular structures with numerous functions. This review focuses on our current understanding of the mechanism of actin nucleation by the Arp2/3 complex and NPFs and how these factors work with other cytoskeletal proteins to generate structurally and functionally diverse actin arrays in cells.
真核细胞利用肌动蛋白聚合作用来改变形状、移动以及通过吞噬作用和胞吞作用内化细胞外物质,并形成收缩结构。此外,一些病原体已经进化出利用宿主细胞肌动蛋白组装来进行附着、内化以及细胞间传播的能力。尽管细胞拥有多种启动肌动蛋白聚合的机制,但在过去五年中,注意力集中在肌动蛋白成核的调控上,即从肌动蛋白单体形成新的肌动蛋白丝。Arp2/3复合物以及调节其活性的多种成核促进因子(NPF)构成了唯一已知的细胞肌动蛋白成核因子,并且可能代表一种在真核生物各门类中保守的通用机制,该机制为具有多种功能的各种细胞结构产生新的肌动蛋白丝。本综述重点关注我们目前对Arp2/3复合物和NPF介导的肌动蛋白成核机制的理解,以及这些因子如何与其他细胞骨架蛋白协同作用,在细胞中生成结构和功能多样的肌动蛋白阵列。