自噬
细胞生物学
自噬体
生物发生
PI3K/AKT/mTOR通路
袋3
神经退行性变
化学
调节器
生物
磷脂酰肌醇
激酶
ULK1
信号转导
蛋白激酶A
生物化学
细胞凋亡
基因
医学
疾病
病理
安普克
作者
Sandra Malmgren Hill,Lidia Wróbel,Avraham Ashkenazi,Marian Fernandez-Estévez,Keith Tan,Roland W. Bürli,David C. Rubinsztein
标识
DOI:10.1038/s41589-020-00726-x
摘要
Autophagy is an essential cellular process that removes harmful protein species, and autophagy upregulation may be able to protect against neurodegeneration and various pathogens. Here, we have identified the essential protein VCP/p97 (VCP, valosin-containing protein) as a novel regulator of autophagosome biogenesis, where VCP regulates autophagy induction in two ways, both dependent on Beclin-1. Utilizing small-molecule inhibitors of VCP ATPase activity, we show that VCP stabilizes Beclin-1 levels by promoting the deubiquitinase activity of ataxin-3 towards Beclin-1. VCP also regulates the assembly and activity of the Beclin-1-containing phosphatidylinositol-3-kinase (PI3K) complex I, thus regulating the production of PI(3)P, a key signaling lipid responsible for the recruitment of downstream autophagy factors. A decreased level of VCP, or inhibition of its ATPase activity, impairs starvation-induced production of PI(3)P and limits downstream recruitment of WIPI2, ATG16L and LC3, thereby decreasing autophagosome formation, illustrating an important role for VCP in early autophagy initiation.
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