Autophagy machinery in the context of mammalian mitophagy

被引:139
作者
Yoshii, Saori R. [1 ]
Mizushima, Noboru [2 ,3 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Physiol & Cell Biol, Bunkyo Ku, Tokyo 1138519, Japan
[2] Univ Tokyo, Grad Sch, Dept Biochem & Mol Biol, Bunkyo Ku, Tokyo 1130033, Japan
[3] Univ Tokyo, Fac Med, Bunkyo Ku, Tokyo 1130033, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2015年 / 1853卷 / 10期
基金
日本学术振兴会;
关键词
Two-step model; Mitophagy; Parkin; Selective autophagy; PARKIN-MEDIATED MITOPHAGY; ENDOPLASMIC-RETICULUM; SELECTIVE AUTOPHAGY; SYNTAXIN; 17; MITOCHONDRIAL TRANSLOCATION; DEPOLARIZED MITOCHONDRIA; DAMAGED MITOCHONDRIA; REGULATES MITOPHAGY; ACTIVATE PARKIN; FORMATION SITE;
D O I
10.1016/j.bbamcr.2015.01.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Autophagy is an intracellular catabolic system that degrades cytoplasmic proteins and organelles. Damaged mitochondria can be degraded by a selective type of autophagy, which is termed mitophagy. PINK1-Parkin-dependent mitophagy has been extensively studied in the mammalian system. PINK1 accumulates on damaged mitochondria to recruit Parkin, which subsequently ubiquitinates a broad range of outer mitochondrial membrane proteins. Ubiquitinated mitochondria associate with the autophagosome formation site, and are selectively incorporated into autophagosomes. During this process, damaged mitochondria first associate with the autophagosome formation site together with upstream autophagy factors, then are efficiently incorporated into autophagosomes through binding with autophagosome adaptors. This "two-step model" may be applied to other selective types of autophagy. This article is part of a Special Issue entitled: Mitophagy. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:2797 / 2801
页数:5
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