The autophagic roles of Rab small GTPases and their upstream regulators A review

被引:118
作者
Szatmari, Zsuzsanna [1 ]
Sass, Miklos [1 ]
机构
[1] Eotvos Lorand Univ, Dept Anat Cell & Dev Biol, Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
autophagy; GAP; GEF; RAB; small GTPases; HUNTINGTONS-DISEASE; ENDOPLASMIC-RETICULUM; PREAUTOPHAGOSOMAL STRUCTURE; SELECTIVE AUTOPHAGY; PARKINSONS-DISEASE; MULTIVESICULAR BODIES; ENDOSOME MATURATION; RECYCLING ENDOSOME; PROMOTES AUTOPHAGY; SECRETORY PATHWAY;
D O I
10.4161/auto.29395
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Macroautophagy is an evolutionarily conserved degradative process of eukaryotic cells. Double-membrane vesicles called autophagosomes sequester portions of cytoplasm and undergo fusion with the endolysosomal pathway in order to degrade their content. There is growing evidence that members of the small GTPase RAB protein family-the well-known regulators of membrane trafficking and fusion events-play key roles in the regulation of the autophagic process. Despite numerous studies focusing on the functions of RAB proteins in autophagy, the importance of their upstream regulators in this process emerged only in the past few years. In this review, we summarize recent advances on the effects of RABs and their upstream modulators in the regulation of autophagy. Moreover, we discuss how impairment of these proteins alters the autophagic process leading to several generally known human diseases.
引用
收藏
页码:1154 / 1166
页数:13
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