Inhibition of glycogen synthase kinase 3β is involved in the resistance to oxidative stress in neuronal HT22 cells

被引:79
作者
Schäfer, M
Goodenough, S
Moosmann, B
Behl, C
机构
[1] Max Planck Inst Psychiat, Independent Res Grp Neurodengenerat, Munich, Germany
[2] Univ Mainz, Sch Med, Dept Pathobiochem, Mainz, Germany
关键词
oxidative stress; oxidation-resistant cell; glycogen synthase kinase 3 beta;
D O I
10.1016/j.brainres.2004.01.037
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oxidative stress is involved in several neurodegenerative diseases including Alzheimer's disease, Parkinson's disease and ischemic reperfusion injury (stroke). We have established clones of the murine hippocampal neuronal cell line HT22, which are resistant to the oxidative stress-causing agents glutamate and hydrogen peroxide, respectively. These cell clones show a mutual cross-resistance to other oxidative stressors, but not to essentially non-oxidative neurotoxins. We have discovered that the amount of phosphorylated, inactive glycogen synthase kinase (GSK) 3beta is elevated in both resistant clones. Pharmacological inhibition of GSK-3beta with lithium chloride in the sensitive parental neuronal cells results in an increased tolerance to glutamate and hydrogen peroxide, suggesting that GSK-3beta is involved in the control of oxidative stress resistance in these cells. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 89
页数:6
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