期刊
BRAIN
卷 135, 期 -, 页码 2865-2874出版社
OXFORD UNIV PRESS
DOI: 10.1093/brain/aws208
关键词
amyotrophic lateral sclerosis; calcium; cyclophilin D; oestrogen; mitochondria; SOD1; transgenic mice
资金
- Robert Packard Center for ALS Research
- Muscular Dystrophy Association
- National Institutes of Health [RO1-NS051419, RO1-NS062055]
Amyotrophic lateral sclerosis is a devastating neurodegenerative disorder that is more prevalent in males than in females. A similar gender difference has been reported in some strains of transgenic mouse models of familial amyotrophic lateral sclerosis harbouring the G93A mutation in CuZn superoxide dismutase. Mitochondrial damage caused by pathological alterations in Ca2+ accumulation is frequently involved in neurodegenerative diseases, including CuZn superoxide dismutase-related amyotrophic lateral sclerosis, but its association with gender is not firmly established. In this study, we examined the effects of genetic ablation of cyclophilin D on gender differences in mice expressing G93A mutant CuZn superoxide dismutase. Cyclophilin D is a mitochondrial protein that promotes mitochondrial damage from accumulated Ca2+. As anticipated, we found that cyclophilin D ablation markedly increased Ca2+ retention in brain mitochondria of both males and females. Surprisingly, cyclophilin D ablation completely abolished the phenotypic advantage of G93A females, with no effect on disease in males. We also found that the 17 beta-oestradiol decreased Ca2+ retention in brain mitochondria, and that cyclophilin D ablation abolished this effect. Furthermore, 17 beta-oestradiol protected G93A cortical neurons and spinal cord motor neurons against glutamate toxicity, but the protection was lost in neurons lacking cyclophilin D. Taken together, these results identify a novel mechanism of oestrogen-mediated neuroprotection in CuZn superoxide dismutase-related amyotrophic lateral sclerosis, whereby Ca2+ overload and mitochondrial damage are prevented in a cyclophilin D-dependent manner. Such a protective mechanism may contribute to the lower incidence and later onset of amyotrophic lateral sclerosis, and perhaps other chronic neurodegenerative diseases, in females.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据