Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA; email:
Lyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.
Annu Rev Biochem. 2018 Jun 20;87:871-896. doi: 10.1146/annurev-biochem-062917-012644. Epub 2018 Apr 16.
Clathrin-mediated endocytosis (CME) is the major endocytic pathway in mammalian cells. It is responsible for the uptake of transmembrane receptors and transporters, for remodeling plasma membrane composition in response to environmental changes, and for regulating cell surface signaling. CME occurs via the assembly and maturation of clathrin-coated pits that concentrate cargo as they invaginate and pinch off to form clathrin-coated vesicles. In addition to the major coat proteins, clathrin triskelia and adaptor protein complexes, CME requires a myriad of endocytic accessory proteins and phosphatidylinositol lipids. CME is regulated at multiple steps-initiation, cargo selection, maturation, and fission-and is monitored by an endocytic checkpoint that induces disassembly of defective pits. Regulation occurs via posttranslational modifications, allosteric conformational changes, and isoform and splice-variant differences among components of the CME machinery, including the GTPase dynamin. This review summarizes recent findings on the regulation of CME and the evolution of this complex process.
网格蛋白介导的内吞作用(CME)是哺乳动物细胞中的主要内吞途径。它负责摄取跨膜受体和转运蛋白,响应环境变化重塑质膜组成,并调节细胞表面信号转导。CME 通过网格蛋白包被陷窝的组装和成熟来发生,陷窝浓缩货物,同时向内凹陷并脱落形成网格蛋白包被囊泡。除了主要的衣壳蛋白、网格蛋白三聚体和衔接蛋白复合物外,CME 还需要大量的内吞辅助蛋白和磷脂酰肌醇脂质。CME 在多个步骤(起始、货物选择、成熟和分裂)受到调节,并通过内吞检查点监测,该检查点诱导有缺陷的陷窝解组装。调节通过翻译后修饰、变构构象变化以及网格蛋白内吞机制组件(包括 GTPase 动力蛋白)的同工型和剪接变体差异发生。本综述总结了 CME 调节和这个复杂过程进化的最新发现。