The University of Queensland, The Institute for Molecular Bioscience, Brisbane, Queensland 4072, Australia.
Curr Opin Cell Biol. 2010 Aug;22(4):519-27. doi: 10.1016/j.ceb.2010.04.001. Epub 2010 May 1.
Eukaryotic cells deftly coordinate an array of endocytic pathways beyond the classical clathrin-mediated endocytic route. Although the existence of clathrin-independent endocytic pathways has been accepted for some time, only recently have tools been developed that specifically delineate their fine details, including molecular composition and ultrastructural morphology. Identification of the salient features of distinct pathways has concomitantly attributed them with specific roles during important cellular processes. Insight from model organisms confirms these roles and suggests maintenance of crucially adapted functions across species. Among other roles, clathrin-independent endocytosis has now been linked to plasma membrane repair, cellular spreading, cellular polarization, and modulation of intercellular signaling. The field is now primed to identify how these pathways function within physiologically relevant environments.
真核细胞巧妙地协调了一系列胞吞途径,超越了经典的网格蛋白介导的胞吞途径。尽管无网格蛋白依赖的胞吞途径的存在已经被接受了一段时间,但直到最近才开发出了专门描述其精细细节的工具,包括分子组成和超微结构形态。对不同途径显著特征的鉴定,同时赋予了它们在重要细胞过程中的特定作用。来自模式生物的研究结果证实了这些作用,并表明这些功能在不同物种中得以维持。除其他作用外,无网格蛋白内吞作用现在与质膜修复、细胞扩展、细胞极化和细胞间信号转导的调节有关。该领域现在已经准备好确定这些途径在生理相关环境中的功能。