Autophagy-related gene Atg5 is essential for astrocyte differentiation in the developing mouse cortex

被引:63
|
作者
Wang, Shukun [1 ,2 ]
Li, Baoguo [1 ,2 ]
Qiao, Huimin [1 ,2 ]
Lv, Xiaohui [1 ]
Liang, Qingli [1 ,2 ]
Shi, Zixiao [1 ,2 ]
Xia, Wenlong [1 ]
Ji, Fen [1 ]
Jiao, Jianwei [1 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Reprod Biol, Beijing, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
基金
美国国家科学基金会;
关键词
astrocyte differentiation; autophagy; cortical development; CENTRAL-NERVOUS-SYSTEM; MOLECULAR-MECHANISMS; DNA METHYLATION; NEURONS; CELLS; SPECIFICATION; GLIOGENESIS; INVOLVEMENT; ONSET; SOCS;
D O I
10.15252/embr.201338343
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Astrocyte differentiation is essential for late embryonic brain development, and autophagy is active during this process. However, it is unknown whether and how autophagy regulates astrocyte differentiation. Here, we show that Atg5, which is necessary for autophagosome formation, regulates astrocyte differentiation. Atg5 deficiency represses the generation of astrocytes in vitro and in vivo. Conversely, Atg5 overexpression increases the number of astrocytes substantially. We show that Atg5 activates the JAK2-STAT3 pathway by degrading the inhibitory protein SOCS2. The astrocyte differentiation defect caused by Atg5 loss can be rescued by human Atg5 overexpression, STAT3 overexpression, and SOCS2 knockdown. Together, these data demonstrate that Atg5 regulates astrocyte differentiation, with potential implications for brain disorders with autophagy deficiency.
引用
收藏
页码:1053 / 1061
页数:9
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