How do ESCRT proteins control autophagy?

被引:147
作者
Rusten, Tor Erik [1 ,2 ]
Stenmark, Harald [1 ,2 ]
机构
[1] Univ Oslo, Fac Med, Ctr Canc Biomed, N-0310 Oslo, Norway
[2] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Biochem, Inst Canc Res, N-0310 Oslo, Norway
关键词
Autophagy; Endosome; ESCRT; Lysosome; Multivesicular body; Ubiquitin; MULTIVESICULAR BODY; SACCHAROMYCES-CEREVISIAE; MOLECULAR MACHINERY; MAMMALIAN-CELLS; COMPLEX; TRAFFICKING; TRANSPORT; ENDOSOME; HRS; LYSOSOMES;
D O I
10.1242/jcs.050021
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Autophagy, a conserved mechanism for lysosomal degradation of cytoplasmic components, has received much attention recently owing to its importance in tissue remodelling and innate immunity, and because it has been proposed that autophagy protects against cancer and neurodegenerative diseases. Although much of the molecular machinery that mediates autophagy has been identified, there are still aspects of this pathway that remain enigmatic. One open issue is the involvement of endosomal sorting complex required for transport (ESCRT) proteins, which were originally identified for their role in sorting ubiquitylated membrane proteins into multivesicular bodies. In this Opinion article, we discuss four possible models that could explain the observation that autophagosomes accumulate in ESCRT-depleted cells. We propose that the involvement of ESCRT proteins in the fusion of autophagosomes with the endolysosomal system is the most plausible model.
引用
收藏
页码:2179 / 2183
页数:5
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