Autophagic lysosomal reformation depends on mTOR reactivation in H2O2-induced autophagy

Int J Biochem Cell Biol. 2016 Jan:70:76-81. doi: 10.1016/j.biocel.2015.11.009. Epub 2015 Nov 14.

Abstract

Autophagic lysosomal reformation, a key cellular process for maintaining lysosome homeostasis in elevated autophagy, so far has only been reported for cells under certain forms of starvation. For this reason, it is controversial that whether this phenomenon is starvation-specific and its importance in lysosomal regeneration at the late stage of autophagy is often challenged. Here we show that exogenous hydrogen peroxide (H2O2) induced lysosome depletion and recovery characteristic of autophagic lysosomal reformation, and we confirmed the occurrence of autophagic lysosomal reformation after H2O2 treatment by demonstrating Rab7 dissociation from autolysosomes, recruitment of Phosphatidylinositol 4-phosphate (PI4P) and clathrin to the surface of autolysosomes, and the existence of tubular "pro-lysosome" structures extending from autolysosomes. Similar to starvation, H2O2 caused an initial deactivation and a subsequent reactivation for mTOR, and mTOR reactivation was essential for ALR. Our results provided a first non-starvation example of autophagic lysosomal reformation and provide evidence for its importance for some autophagic processes other than that of starvation.

Keywords: Autophagic lysosomal reformation; Autophagy; Hydrogen peroxide; Starvation; mTOR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagy / drug effects*
  • Autophagy / genetics
  • Clathrin / genetics
  • Clathrin / metabolism
  • Culture Media / chemistry
  • Culture Media / pharmacology
  • Gene Expression Regulation
  • Genes, Reporter
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • HeLa Cells
  • Homeostasis / genetics
  • Humans
  • Hydrogen Peroxide / pharmacology*
  • Lysosomes / drug effects*
  • Lysosomes / metabolism
  • Lysosomes / ultrastructure
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Phagosomes / drug effects*
  • Phagosomes / metabolism
  • Phagosomes / ultrastructure
  • Phosphatidylinositol Phosphates / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism*
  • rab GTP-Binding Proteins / genetics
  • rab GTP-Binding Proteins / metabolism
  • rab7 GTP-Binding Proteins

Substances

  • Clathrin
  • Culture Media
  • MAP1LC3A protein, human
  • Microtubule-Associated Proteins
  • Phosphatidylinositol Phosphates
  • Recombinant Fusion Proteins
  • phosphatidylinositol 4-phosphate
  • rab7 GTP-Binding Proteins
  • rab7 GTP-binding proteins, human
  • Green Fluorescent Proteins
  • Hydrogen Peroxide
  • MTOR protein, human
  • TOR Serine-Threonine Kinases
  • rab GTP-Binding Proteins