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MCOLN/TRPML channels in the regulation of MTORC1 and autophagy.
Huang, Peng; Dong, Rose Yang; Wang, Pingping; Xu, Mengnan; Sun, Xue; Dong, Xian-Ping.
Afiliação
  • Huang P; Chongming Hospital, Shanghai University of Medicine and Health Sciences, Shanghai, China.
  • Dong RY; Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Wang P; Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Xu M; Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Sun X; Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Dong XP; Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia, Canada.
Autophagy ; 20(5): 1203-1204, 2024 05.
Article em En | MEDLINE | ID: mdl-38180017
ABSTRACT
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Autofagia / Alvo Mecanístico do Complexo 1 de Rapamicina Limite: Animals / Humans Idioma: En Revista: Autophagy Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Autofagia / Alvo Mecanístico do Complexo 1 de Rapamicina Limite: Animals / Humans Idioma: En Revista: Autophagy Ano de publicação: 2024 Tipo de documento: Article