共 115 条
Regulation of autophagy by the Rab GTPase network
被引:373
作者:
Ao, X.
[1
]
Zou, L.
[2
]
Wu, Y.
[2
]
机构:
[1] Third Mil Med Univ, PLA, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, PLA, Inst Immunol, Chongqing 400038, Peoples R China
基金:
中国国家自然科学基金;
美国国家科学基金会;
关键词:
autophagy;
autophagosome;
Rab GTPase;
HEPATITIS-C VIRUS;
GROUP-A STREPTOCOCCUS;
ENDOPLASMIC-RETICULUM;
SELECTIVE AUTOPHAGY;
PROMOTES AUTOPHAGY;
TRAPP COMPLEXES;
ALPHA-SYNUCLEIN;
PREAUTOPHAGOSOMAL STRUCTURE;
SACCHAROMYCES-CEREVISIAE;
MULTIVESICULAR BODIES;
D O I:
10.1038/cdd.2013.187
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 (macroautophagy) is a highly conserved intracellular and lysosome-dependent degradation process in which autophagic substrates are enclosed and degraded by a double-membrane vesicular structure in a continuous and dynamic vesicle transport process. The Rab protein is a small GTPase that belongs to the Ras-like GTPase superfamily and regulates the vesicle traffic process. Numerous Rab proteins have been shown to be involved in various stages of autophagy. Rab1, Rab5, Rab7, Rab9A, Rab11, Rab23, Rab32, and Rab33B participate in autophagosome formation, whereas Rab9 is required in non-canonical autophagy. Rab7, Rab8B, and Rab24 have a key role in autophagosome maturation. Rab8A and Rab25 are also involved in autophagy, but their role is unknown. Here, we summarize new findings regarding the involvement of Rabs in autophagy and provide insights regarding future research on the mechanisms of autophagy regulation.
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页码:348 / 358
页数:11
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