Chondrocyte apoptosis induced by hydrogen peroxide requires caspase activation but not mitochondrial pore transition

被引:61
作者
Lo, MY
Kim, HT
机构
[1] Vet Adm Med Ctr, San Francisco, CA 94121 USA
[2] Univ Calif San Francisco, Dept Orthopaed Surg, San Francisco, CA 94143 USA
关键词
cartilage; apoptosis; caspase; mitochondria; peroxide;
D O I
10.1016/j.orthres.2003.12.022
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The primary objective of this study was to test the hypothesis that inhibition of mitochondrial permeability transition and/or inhibition of caspase family enzymes can block chondrocyte apoptosis induced by H2O2. Primary human chondrocytes were isolated from normal cartilage by enzymatic digestion. Apoptosis was induced by exposure to H2O2. Chondrocyte apoptosis was quantified using an ELISA for nucleosome formation. Independent confirmation of apoptosis was obtained by TUNEL analysis. H2O2 induced apoptosis in primary human chondrocytes in a time and dose dependent manner. The effects of candidate apoptosis inhibitors were then tested. Chondrocytes were pre-treated with inhibitors of mitochondrial permeability transition, or one of three different caspase inhibitors, and then incubated with H2O2. Apoptosis was then measured after 16 h of exposure to H2O2. Pre-treatment with inhibitors of mitochondrial permeability transition did not block apoptosis induced by H2O2. A non-selective caspase inhibitor, a caspase 3-selective inhibitor, and a caspase 1-selective inhibitor, all blocked chondrocyte apoptosis induced by H2O2. These results show that H2O2 triggers chondrocyte apoptosis through caspase activation, independent of mitochondrial membrane permeability transition. (C) 2004 Orthopaedic Research Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1120 / 1125
页数:6
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