Manganese superoxide dismutase protects from TNF-alpha-induced apoptosis by increasing the steady-state production of H2O2

Antioxid Redox Signal. Jul-Aug 2006;8(7-8):1295-305. doi: 10.1089/ars.2006.8.1295.


Manganese superoxide dismutase (SOD2) has been well established to be essential for protection from a variety of apoptotic stimuli. Here we demonstrate that the antiapoptotic effects of SOD2 are attributed to its ability to generate H(2)O(2) and that its efficient removal resensitizes cells to tumor necrosis factor (TNF)-alpha-induced apoptosis. SOD2 overexpression in HT-1080 cells leads to a decrease in the fluorescence of the superoxidesensitive fluorophore, dihydroethidium, and a concomitant increase in oxidation of the H2O2-sensitive dye, dichlorodihydrofluorescein diacetate (DCFDA). The rate of aminotriazole-inhibited catalase activity also was increased when SOD2 is overexpressed and reflects a 1.6-fold increase in the steady-state production of H(2)O(2). The increase in H(2)O(2) was associated with decreased sensitivity to TNF-alpha-mediated apoptosis, as measured by monitoring the loss of mitochondrial membrane potential (MMP), caspase activation, poly-ADP ribose polymerase (PARP) cleavage, and accumulation of hypodiploid DNA content. Both the increase in H2O2 and resistance to TNF-mediated apoptosis were reversed by coexpression of catalase. The lipid hydroperoxide scavengers, beta-hydroxytoluene and trolox, and the iron chelator, desferroxamine, showed partial recovery of TNF-induced apoptosis. These findings indicate that increases in the intracellular steady-state production of H(2)O(2) by SOD2 can block the activation of key processes fundamental to the process of programmed cell death.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Amitrole / pharmacology
  • Apoptosis / drug effects*
  • Caspases / metabolism
  • Catalase / analysis
  • Catalase / metabolism
  • Cell Line, Tumor
  • Cycloheximide / pharmacology
  • Cytoprotection / physiology*
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Hydrogen Peroxide / metabolism*
  • Membrane Potentials / drug effects
  • Mitochondria / physiology
  • Oxygen / metabolism
  • Poly(ADP-ribose) Polymerases / metabolism
  • Protein Synthesis Inhibitors / pharmacology
  • Recombinant Proteins / metabolism
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism*
  • Time Factors
  • Transfection
  • Tumor Necrosis Factor-alpha / pharmacology*


  • Enzyme Inhibitors
  • Protein Synthesis Inhibitors
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Cycloheximide
  • Hydrogen Peroxide
  • Catalase
  • Superoxide Dismutase
  • Poly(ADP-ribose) Polymerases
  • Caspases
  • Oxygen
  • Amitrole