Hydrogen peroxide (H2O2) is known to both induce and inhibit apoptosis, however the mechanisms are unclear. We found that H2O2 inhibited the activity of recombinant caspase-3 and caspase-8, half-inhibition occurring at about 17 muM H2O2, This inhibition was both prevented and reversed by dithiothreitol while glutathione had little protective effect, 100-200 muM H2O2 added to macrophages after induction of caspase activation by nitric oxide or serum withdrawal substantially inhibited caspase activity. Activation of H2O2-producing NADPH oxidase in macrophages also caused catalase-sensitive inactivation of cellular caspases. The data suggest that the activity of caspases in cells can be directly but reversibly inhibited by H2O2. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
机构:
Univ Rochester, Sch Med & Dent, Cardiol Unit, Cardiovasc Res Ctr, Rochester, NY 14642 USAUniv Rochester, Sch Med & Dent, Cardiol Unit, Cardiovasc Res Ctr, Rochester, NY 14642 USA
Abe, J
;
Berk, BC
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机构:
Univ Rochester, Sch Med & Dent, Cardiol Unit, Cardiovasc Res Ctr, Rochester, NY 14642 USAUniv Rochester, Sch Med & Dent, Cardiol Unit, Cardiovasc Res Ctr, Rochester, NY 14642 USA
机构:
Univ Rochester, Sch Med & Dent, Cardiol Unit, Cardiovasc Res Ctr, Rochester, NY 14642 USAUniv Rochester, Sch Med & Dent, Cardiol Unit, Cardiovasc Res Ctr, Rochester, NY 14642 USA
Abe, J
;
Berk, BC
论文数: 0引用数: 0
h-index: 0
机构:
Univ Rochester, Sch Med & Dent, Cardiol Unit, Cardiovasc Res Ctr, Rochester, NY 14642 USAUniv Rochester, Sch Med & Dent, Cardiol Unit, Cardiovasc Res Ctr, Rochester, NY 14642 USA