Doherty Gary J, McMahon Harvey T
MRC Laboratory of Molecular Biology, Cambridge, United Kingdom.
Annu Rev Biochem. 2009;78:857-902. doi: 10.1146/annurev.biochem.78.081307.110540.
Endocytic mechanisms control the lipid and protein composition of the plasma membrane, thereby regulating how cells interact with their environments. Here, we review what is known about mammalian endocytic mechanisms, with focus on the cellular proteins that control these events. We discuss the well-studied clathrin-mediated endocytic mechanisms and dissect endocytic pathways that proceed independently of clathrin. These clathrin-independent pathways include the CLIC/GEEC endocytic pathway, arf6-dependent endocytosis, flotillin-dependent endocytosis, macropinocytosis, circular doral ruffles, phagocytosis, and trans-endocytosis. We also critically review the role of caveolae and caveolin1 in endocytosis. We highlight the roles of lipids, membrane curvature-modulating proteins, small G proteins, actin, and dynamin in endocytic pathways. We discuss the functional relevance of distinct endocytic pathways and emphasize the importance of studying these pathways to understand human disease processes.
内吞机制控制着质膜的脂质和蛋白质组成,从而调节细胞与周围环境的相互作用方式。在此,我们综述了目前已知的哺乳动物内吞机制,重点关注控制这些过程的细胞蛋白。我们讨论了研究充分的网格蛋白介导的内吞机制,并剖析了独立于网格蛋白的内吞途径。这些不依赖网格蛋白的途径包括CLIC/GEEC内吞途径、arf6依赖性内吞作用、flotillin依赖性内吞作用、巨胞饮作用、环形背侧褶皱、吞噬作用和转胞吞作用。我们还严格审视了小窝和小窝蛋白1在内吞作用中的作用。我们强调了脂质、膜曲率调节蛋白、小G蛋白、肌动蛋白和发动蛋白在内吞途径中的作用。我们讨论了不同内吞途径的功能相关性,并强调研究这些途径对于理解人类疾病过程的重要性。