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Down-regulated reactive oxygen species by HSP90 in 3HK-induced SKN-SH cell death
Affiliation:1. Department of Neurology, Seoul National University, College of Medicine, Seoul, Korea;2. Department of Critical Care Medicine, Seoul National University Hospital, Seoul, South Korea;3. Department of Neurology, Inha University Hospital, Incheon, South Korea
Abstract:In this present study, we show that 3HK induced reactive oxygen species (ROS) accumulation and after caspase activation lead to apoptotic cell death. Pretreatment with N-acetylcysteine (NAC), an effective antioxidant, significantly attenuated 3HK-induced apoptosis by way of a reduction of ROS accumulation and caspase activity. SKN-SN cells were protected from 3HK-induced cytotoxicity by heat shock protein (HSP). HSP effectively attenuated 3HK-mediated ROS accumulation and apoptosis. In addition, the protective effect of HSP90 was abolished by pretreatment with HSP90 anti-sense oligonucleotides, but not when pretreated with anti-senses for other HSPs. These results suggest that HSP90 protects SKN-SH cells from 3HK-induced cytotoxicity by reducing ROS levels and caspase activity.
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