mTORC1型
自噬
细胞生物学
生物
溶酶体
磷脂酰肌醇
液泡
PI3K/AKT/mTOR通路
生物化学
信号转导
酶
细胞质
细胞凋亡
作者
Peng Huang,Rose Yang Dong,Pingping Wang,Mengnan Xu,Xue Sun,Xian‐Ping Dong
出处
期刊:Autophagy
[Informa]
日期:2024-01-05
卷期号:20 (5): 1203-1204
被引量:2
标识
DOI:10.1080/15548627.2023.2300922
摘要
MCOLN1 and MCOLN3 are two Ca2+ release channels residing in the endolysosomal membrane. They are activated by phosphatidylinositol (PtdIns)-3-phosphate (PtdIns3P) and/or PtdIns(3,5)P2. Their activities are also regulated by lumenal pH, with low pH enhancing that of MCOLN1 and high pH increasing that of MCOLN3. Recent studies further suggest that upon starvation, both MCOLN1 and MCOLN3 are activated by a reduction in MTORC1 activity; their activation in turn regulates MTORC1 activity to facilitate macroautophagic/autophagic flux. On the one hand, MCOLN3 appears to be recruited to phagophores where it is activated by PtdIns3P and high pH to inhibit MTORC1 activity using a positive feedback mechanism, thereby increasing autophagy induction. On the other hand, MCOLN1 is activated by PtdIns(3,5)P2 and low pH in (auto)lysosomes to increase MTORC1 activity using a negative feedback mechanism, promoting autophagic lysosome reformation. The cell uses the two feedback mechanisms to ensure efficient autophagic flux to survive adverse conditions such as nutrient deprivation and bacterial infection.
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