Coupling between clathrin-coated-pit invagination, cortactin recruitment, and membrane scission observed in live cells

被引:360
作者
Merrifield, CJ
Perrais, D
Zenisek, D
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[2] CNRS, UMR 5091, Lab Physiol Cellulaire Synapse, F-33077 Bordeaux, France
[3] Univ Bordeaux 2, Inst Francois Magendie, F-33077 Bordeaux, France
[4] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06520 USA
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.cell.2005.03.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During clathrin-mediated endocytosis, membrane scission marks the isolation of a cargo-laden clathrin-coated pit (CCP) from the cell exterior. Here we used live-cell imaging of a pH-sensitive cargo to visualize the formation of clathrin-coated vesicles (CCVs) at single CCPs with a time resolution of seconds. We show that CCPs are highly dynamic and can produce multiple vesicles in succession. Using alternating evanescent field and epifluorescence illumination, we show that CCP invagination and scission are tightly coupled, with scission coinciding with maximal displacement of CCPs from the plasma membrane and with peak recruitment of cortactin-DsRed, a dynamin and F-actin binding protein. Finally, perturbing actin polymerization with latrunculin-B drastically reduces the efficiency of membrane scission and affects many aspects of CCP dynamics. We propose that CCP invagination, actin polymerization, and CCV formation are highly coordinated for efficient endocytosis.
引用
收藏
页码:593 / 606
页数:14
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