Regulation of Vps4 During MVB Sorting and Cytokinesis

被引:44
作者
Babst, Markus [1 ]
Davies, Brian A. [2 ]
Katzmann, David J. [2 ]
机构
[1] Univ Utah, Dept Biol, Salt Lake City, UT 84112 USA
[2] Mayo Clin, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
关键词
cytokinesis; endocytosis; ESCRT; MVB pathway; protein trafficking; AAA-ATPASE VPS4; MULTIVESICULAR BODY PATHWAY; ESCRT-III RECOGNITION; STRUCTURAL BASIS; PROTEIN INTERACTIONS; MEMBRANE SCISSION; COMPLEX; ENDOSOME; AUTOINHIBITION; FILAMENTS;
D O I
10.1111/j.1600-0854.2011.01230.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multivesicular body (MVB) formation is the result of invagination and budding of the endosomal limiting membrane into its intralumenal space. These intralumenal vesicles (ILVs) contain a subset of endosomal transmembrane cargoes destined for degradation within the lysosome, the result of active selection during MVB sorting. Membrane bending and scission during ILV formation is topologically similar to cytokinesis in that both events require the abscission of a membrane neck that is oriented away from the cytoplasm. The endosomal sorting complexes required for transport (ESCRTs) represent cellular machinery whose function makes essential contributions to both of these processes. In particular, the AAA-ATPase Vps4 and its substrate ESCRT-III are key components that seem to execute the membrane abscission reaction. This review summarizes current knowledge about the Vps4-ESCRT-III system and discusses a model for how the recruitment of Vps4 to the different sites of function might be regulated.
引用
收藏
页码:1298 / 1305
页数:8
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