Merrifield Christien J
MRC Laboratory of Molecular Biology, Division of Cell Biology, Cambridge CB2 2QH, UK.
Trends Cell Biol. 2004 Jul;14(7):352-8. doi: 10.1016/j.tcb.2004.05.008.
Endocytosis is characterized by movement and precisely controlled changes in membrane geometry during vesicle formation. Recent developments in live-cell imaging have enabled such movements to be monitored in vivo and correlated with the recruitment and dismissal of fluorescently labeled proteins. This experimental strategy has revealed the sequential recruitment of proteins that are involved in actin polymerization, and actin to single sites of endocytosis in both yeast and mammalian cells. Actin polymerization is correlated with the inward movements of endocytic organelles, which suggests that actin polymerization has a conserved role in this process. In this article, I will discuss three models for the role of actin polymerization in endocytosis.
内吞作用的特点是在囊泡形成过程中膜几何形状的移动和精确控制的变化。活细胞成像技术的最新进展使得能够在体内监测这种移动,并将其与荧光标记蛋白的募集和解离相关联。这种实验策略揭示了参与肌动蛋白聚合的蛋白以及肌动蛋白在酵母和哺乳动物细胞中内吞作用的单个位点上的顺序募集。肌动蛋白聚合与内吞细胞器的向内移动相关,这表明肌动蛋白聚合在这一过程中具有保守作用。在本文中,我将讨论肌动蛋白聚合在内吞作用中作用的三种模型。