MCOLN/TRPML channels in the regulation of MTORC1 and autophagy

被引:4
|
作者
Huang, Peng [1 ,2 ]
Dong, Rose Yang [1 ]
Wang, Pingping [1 ]
Xu, Mengnan [1 ]
Sun, Xue [1 ,3 ]
Dong, Xian-Ping [1 ,4 ]
机构
[1] Dalhousie Univ, Dept Physiol & Biophys, Halifax, NS, Canada
[2] Shanghai Univ Med & Hlth Sci, Chongming Hosp, Shanghai, Peoples R China
[3] China Med Univ, Dept Dev Cell Biol, Shenyang, Liaoning, Peoples R China
[4] Dalhousie Univ, Dept Physiol & Biophys, Sir Charles Tupper Med Bldg,5850 Coll St, Halifax, NS B3H 4R2, Canada
基金
加拿大健康研究院;
关键词
Autophagy; MCOLN1; MCOLN3; MTORC1; TRPML1; TRPML3;
D O I
10.1080/15548627.2023.2300922
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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)P-2. 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)P-2 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.
引用
收藏
页码:1203 / 1204
页数:2
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