Alkaline stress-induced autophagy is mediated by mTORC1 inactivation

J Cell Biochem. 2011 Sep;112(9):2566-73. doi: 10.1002/jcb.23181.

Abstract

The activation of autophagic pathway by alkaline stress was investigated. Various types of mammalian cells were subjected to alkaline stress by incubation in bicarbonate buffered media in humidified air containing atmospheric 0.04% CO(2) . The induction of autophagy following alkaline stress was evaluated by assessing the conversion of cytosolic LC3-I into lipidated LC3-II, the accumulation of autophagosomes, and the formation of autolysosomes. Colocalization of GFP-LC3 with endolysosomal marker in HeLa GFP-LC3 cells undergoing autophagic process by alkaline stress further demonstrates that autophagosomes triggered by alkaline stress matures into autolysosomes for the lysosome dependent degradation. We found that the inactivation of mTORC1 is important for the pathway leading to the induction of autophagy by alkaline stress since the expression of RhebQ64L, a constitutive activator of mTORC1, downregulates the induction of autophagy after alkaline stress in transfected human 293T cells. These results imply that activation of autophagic pathway following the inactivation of mTORC1 is important cellular events governing alkaline stress-induced cytotoxicity and clinical symptoms associated with alkalosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkalosis / metabolism
  • Alkalosis / physiopathology*
  • Autophagy*
  • Cell Size
  • Down-Regulation
  • Enzyme Activation
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Lysosomes / metabolism
  • Mechanistic Target of Rapamycin Complex 1
  • Microtubule-Associated Proteins / metabolism
  • Monomeric GTP-Binding Proteins / genetics
  • Monomeric GTP-Binding Proteins / metabolism
  • Multiprotein Complexes
  • Mutation, Missense
  • Neuropeptides / genetics
  • Neuropeptides / metabolism
  • Phagosomes / metabolism
  • Proteins / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Ras Homolog Enriched in Brain Protein
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction
  • Stress, Physiological*
  • TOR Serine-Threonine Kinases

Substances

  • MAP1LC3A protein, human
  • Microtubule-Associated Proteins
  • Multiprotein Complexes
  • Neuropeptides
  • Proteins
  • RHEB protein, human
  • Ras Homolog Enriched in Brain Protein
  • Recombinant Fusion Proteins
  • Mechanistic Target of Rapamycin Complex 1
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • Monomeric GTP-Binding Proteins