Impairment of Na(+),K(+)-ATPase in CD95(APO-1)-induced human T-cell leukemia cell apoptosis mediated by glutathione depletion and generation of hydrogen peroxide

Leukemia. 2007 Aug;21(8):1669-78. doi: 10.1038/sj.leu.2404791. Epub 2007 Jun 7.

Abstract

Human T-cell leukemia is a malignant disease that needs various regimens of cytotoxic chemotherapy to overcome drug resistance. Recently, Na(+),K(+)-ATPase has emerged as a potential target for cancer therapy. However, its exact signaling pathway in human T-cell leukemia cell death has not been well defined. In the current study, we found CD95(APO-1) was able to trigger the internalization of plasma membrane Na(+),K(+)-ATPase in Jurkat cells or primary T cells as a mechanism to suppress its activity. This internalization was closely relevant to intracellular glutathione (GSH) depletion in Jurkat cells downstream of Fas-associated death domain protein (FADD) and caspase 8. GSH depletion in Fas L-treated Jurkat cells induced the generation of hydrogen peroxide (H(2)O(2)), which subsequently increased the serine phosphorylation of Na(+),K(+)-ATPase alpha1 subunit. Exogenous H(2)O(2) even mimicked the effect of Fas L to upregulate the serine phosphorylation of Na(+),K(+)-ATPase alpha1 subunit and suppress Na(+),K(+)-ATPase activity. Overall, our results indicate that CD95(APO-1) induces the FADD- and caspase 8-dependent internalization of Na(+),K(+)-ATPase through intracellular GSH loss, and the subsequent generation of H(2)O(2)-mediated serine phosphorylation of Na(+),K(+)-ATPase alpha1 subunit. Taken together, this study presents a novel regulatory mechanism of Na(+),K(+)-ATPase in CD95(APO-1)-mediated human T-leukemia cell apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • Caspase 8 / metabolism
  • Catalase / pharmacology
  • Cell Membrane / metabolism
  • Fas Ligand Protein / metabolism
  • Fas-Associated Death Domain Protein / metabolism
  • Fluorescent Antibody Technique, Indirect
  • Glutathione / metabolism*
  • Humans
  • Hydrogen Peroxide / pharmacology*
  • Immunoblotting
  • Immunoprecipitation
  • Jurkat Cells / drug effects
  • Jurkat Cells / metabolism
  • Leukemia, T-Cell / metabolism
  • Leukemia, T-Cell / pathology*
  • Male
  • Membrane Potentials / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Ouabain / metabolism
  • Oxidants / pharmacology
  • Phosphorylation
  • Receptor-Interacting Protein Serine-Threonine Kinases / metabolism
  • Sodium-Potassium-Exchanging ATPase / antagonists & inhibitors*
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Superoxide Dismutase / metabolism
  • fas Receptor / pharmacology*

Substances

  • Fas Ligand Protein
  • Fas-Associated Death Domain Protein
  • Oxidants
  • fas Receptor
  • Ouabain
  • Hydrogen Peroxide
  • Catalase
  • Superoxide Dismutase
  • RIPK1 protein, human
  • Receptor-Interacting Protein Serine-Threonine Kinases
  • Caspase 8
  • Sodium-Potassium-Exchanging ATPase
  • Glutathione