Hippocampal neurons of mice deficient in DNA-dependent protein kinase exhibit increased vulnerability to DNA damage, oxidative stress and excitotoxicity

被引:66
作者
Culmsee, C
Bondada, S
Mattson, MP
机构
[1] NIA, Gerontol Res Ctr, Neurosci Lab, Baltimore, MD 21224 USA
[2] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40536 USA
[3] Univ Marburg, Inst Pharmakol & Toxikol, D-35037 Marburg, Germany
[4] Univ Kentucky, Dept Microbiol & Immunol, Lexington, KY 40536 USA
[5] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
来源
MOLECULAR BRAIN RESEARCH | 2001年 / 87卷 / 02期
关键词
Alzheimer's disease; amyloid beta-peptide; DNA repair; epileptic seizure; glutamate; topoisomerase inhibitor;
D O I
10.1016/S0169-328X(01)00008-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
DNA damage has been documented in neurodegenerative conditions ranging from Alzheimer's disease to stroke. DNA-dependent protein kinase (DNA-PK) is involved in V(D)J recombination and DNA double strand break repair, and may play a role in cell death induced by DNA damage. We now report that cultured hippocampal neurons from severe combined immunodeficient (scid) mice which lack DNA-PK activity are hypersensitive to apoptosis induced by exposure to topoisomerase inhibitors, amyloid beta peptide (AP) and glutamate. A similar increased vulnerability of hippocampal CAI and CA3 neurons was observed in adult scid mice after kainate-induced seizures. Our results suggest that DNA-PK activity is important for neuron survival under conditions that may occur in neurological disorders. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:257 / 262
页数:6
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