Proteasome inhibitors prevent oxidative stress-induced nerve cell death by a novel mechanism

被引:21
作者
Maher, Pamela [1 ]
机构
[1] Salk Inst Biol Studies, La Jolla, CA 92037 USA
关键词
reactive oxygen species; NF-kappa B; mitochondria; phosphorylation; glutathione;
D O I
10.1016/j.bcp.2008.02.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The role of the proteasome in neurodegenerative diseases is controversial. on the one hand, there is evidence that a dysfunction of proteasome activity can lead to neurodegeneration but there is also data showing that proteasome inhibition can protect nerve cells from a variety of insults. In an attempt to clarify this issue, we studied the effects of four different proteasome inhibitors in a well characterized model of oxidative stress-induced nerve cell death. Consistent with the hypothesis that proteasome inhibition can be neuroprotective, we found that low concentrations of proteasome inhibitors were able to protect nerve cells from oxidative stress-induced death. Surprisingly, the neuroprotective effects of the proteasome inhibitors appeared to be at least partially mediated by the induction of NF-kappa B since protection was significantly reduced in cells expressing a specific NF-kappa B repressor. The activation of NF-kB by proteasome inhibitors was mediated by I kappa B alpha and IKK and was blocked by antioxidants and inhibitors of mitochondrial reactive oxygen species production. These data suggest that low concentrations of proteasome inhibitors induce a moderate level of mitochondrial oxidative stress which results in the activation of neuroprotective pathways. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1994 / 2006
页数:13
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