Nitric oxide protects macrophages from hydrogen peroxide-induced apoptosis by inducing the formation of catalase

J Immunol. 2006 Apr 15;176(8):4675-81. doi: 10.4049/jimmunol.176.8.4675.

Abstract

We investigated the cytoprotective effect of NO on H2O2-induced cell death in mouse macrophage-like cell line RAW264. H2O2-treated cells showed apoptotic features, such as activation of caspase-9 and caspase-3, nuclear fragmentation, and DNA fragmentation. These apoptotic features were significantly inhibited by pretreatment for 24 h with NO donors, sodium nitroprusside and 1-hydroxy-2-oxo-3,3-bis-(2-aminoethyl)-1-triazene, at a low nontoxic concentration. The cytoprotective effect of NO was abrogated by the catalase inhibitor 3-amino-1,2,4-triazole but was not affected by a glutathione synthesis inhibitor, L-buthionine-(S,R)-sulfoximine. NO donors increased the level of catalase and its activity in a concentration-dependent manner. Cycloheximide, a protein synthesis inhibitor, inhibited both the NO-induced increase in the catalase level and the cytoprotective effect of NO. These results indicate that NO at a low concentration protects macrophages from H2O2-induced apoptosis by inducing the production of catalase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Catalase / biosynthesis*
  • Cell Line
  • Cyclic GMP / metabolism
  • Hydrogen Peroxide / toxicity*
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / metabolism*
  • Mice
  • Nitric Oxide / metabolism*
  • Nitric Oxide Donors / pharmacology
  • Nitroprusside / pharmacology
  • Nitroso Compounds / pharmacology
  • Signal Transduction

Substances

  • NOC 18
  • Nitric Oxide Donors
  • Nitroso Compounds
  • Nitroprusside
  • Nitric Oxide
  • Hydrogen Peroxide
  • Catalase
  • Cyclic GMP