| Literature DB >> 25227738 |
Shukun Wang1, Baoguo Li1, Huimin Qiao1, Xiaohui Lv2, Qingli Liang1, Zixiao Shi1, Wenlong Xia2, Fen Ji2, Jianwei Jiao3.
Abstract
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.Entities:
Keywords: astrocyte differentiation; autophagy; cortical development
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Year: 2014 PMID: 25227738 PMCID: PMC4253845 DOI: 10.15252/embr.201338343
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807