Annexin A2-Dependent Polymerization of Actin Mediates Endosome Biogenesis

被引:139
作者
Morel, Etienne [1 ]
Parton, Robert G. [2 ,3 ]
Gruenberg, Jean [1 ]
机构
[1] Univ Geneva, Dept Biochem, CH-1211 Geneva 4, Switzerland
[2] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[3] Univ Queensland, Ctr Microscopy & Microanal, Brisbane, Qld 4072, Australia
关键词
MULTIVESICULAR ENDOSOMES; TRANSPORT; VESICLES; BINDING; ENDOCYTOSIS; PATHWAY; LOCALIZATION; DROSOPHILA; PROTEINS; DYNAMICS;
D O I
10.1016/j.devcel.2009.01.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Early endosomes give rise to multivesicular intermediates during transport toward late endosomes. Much progress has been made in understanding the sorting of receptors into these intermediates, but the mechanisms responsible for their biogenesis remain unclear. Here, we report that F-actin is necessary for transport beyond early endosomes and endosome formation. We found that endosomes captured by actin cables were essentially stationary, but early endosomes also exhibited patches of F-actin and facilitated selective F-actin nucleation and polymerization. Our data show that nucleation of actin patches by early endosomes is strictly dependent on annexin A2, a protein involved in early-to-late endosome transport. It also requires the actin nucleation factor Spirel and involves Arp2/3, which is needed for filament branching. We conclude that actin patches are nucleated on early endosomes via annexin A2 and Spirel, and that these patches control endosome biogenesis, presumably by driving the membrane remodeling process.
引用
收藏
页码:445 / 457
页数:13
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