MTOR, PIK3C3, and autophagy: Signaling the beginning from the end

被引:239
作者
Munson, Michael J. [1 ]
Ganley, Ian G. [1 ]
机构
[1] Univ Dundee, Coll Life Sci, MRC Prot Phosphorylat & Ubiquitylat Unit, Dundee, Scotland
基金
英国医学研究理事会;
关键词
autophagic lysosome reformation; lysosome; MTOR; phosphatidylinositol; 3-phosphate; tubulation; UVRAG; VPS34;
D O I
10.1080/15548627.2015.1106668
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
A key point in starvation-induced autophagy occurs at the end of the process, where lysosomes are regenerated from autolysosomes through a pathway termed autophagic lysosome reformation (ALR). ALR occurs when autolysosomal MTOR becomes reactivated by amino acids derived from the autophagic delivery of protein cargo. This activation not only turns off autophagosome formation but also leads to reformation of lysosomes, ready for the next round of autophagy, through a series of events involving autolysosomal tubulation. We have now found that MTOR regulates multiple steps of ALR including direct activation of the PIK3C3-UVRAG lipid kinase complex to enable autolysosomal tubules to break away and regenerate lysosomes.
引用
收藏
页码:2375 / 2376
页数:2
相关论文
empty
未找到相关数据