Oxidative damage to mitochondrial DNA in spinal motoneurons of transgenic ALS mice

被引:96
作者
Warita, H [1 ]
Hayashi, T [1 ]
Murakami, T [1 ]
Manabe, Y [1 ]
Abe, K [1 ]
机构
[1] Okayama Univ, Sch Med, Dept Neurol, Okayama 700, Japan
来源
MOLECULAR BRAIN RESEARCH | 2001年 / 89卷 / 1-2期
关键词
oxidative stress; mitochondria; SOD1; transgenic mouse; amyotropic lateral sclerosis;
D O I
10.1016/S0169-328X(01)00029-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In order to clarify a possible role of oxidative stress in motoneuron death in amyotrophic lateral sclerosis (ALS), we examined a presence of 8-hydroxy-2-deoxyguanosine (8-OHdG), one of the best markers of the oxidative DNA damage, in the spinal cord of transgenic mice harboring a mutant Cu/Zn superoxide dismutase (SOD1) gene. Immunocytochemistry showed a progressive accumulation of 8-OHdG in ventral horn neurons from early and presymptomatic stage (25 weeks) before significant loss of ventral horn neurons, while no detectable 8-OHdG in non-transgenic control mice. At the late and symptomatic stage (35 weeks), the 8-OHdG-like immunoreactivity spread over the posterior horn of spinal cord in Tg mice. Thr immunoreactivity for 8-OHdG was not localized in the nucleus but in cytoplasm with small granular pattern. These data suggest that an oxidative damage to mitochondrial DNA is happening in spinal motoneurons of the Tg mice from very early stage of the disease, and may be involved in the mechanism of the subsequent motoneuron death in this model. (C) 2001 Elsevier Science B.V. All rights: reserved.
引用
收藏
页码:147 / 152
页数:6
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