Mitochondrial Mutations: Newly Discovered Players in Neuronal Degeneration

被引:47
作者
Lax, Nichola Z. [2 ]
Turnbull, Doug M. [2 ]
Reeve, Amy K. [1 ,2 ]
机构
[1] Newcastle Univ, Mitochondrial Res Grp, Sch Med, Inst Ageing & Hlth, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Newcastle Univ, Ctr Brain Ageing & Vital, Inst Ageing & Hlth, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
英国惠康基金; 英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
mitochondria; mitochondrial DNA; neurodegeneration; neuropathology; cell death; COMPLEX I DEFICIENCY; ALPHA-SYNUCLEIN; DNA MUTATIONS; AMYLOID-BETA; MYOCLONIC EPILEPSY; POINT MUTATIONS; POLG MUTATIONS; CYTOCHROME-C; DISEASE; ALZHEIMERS;
D O I
10.1177/1073858411385469
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Mutations in mitochondria! DNA cause a number of neurological diseases with defined neuropathology; however, mutations in this genome have also been found to be important in a number of more common neurodegenerative diseases. In this review, the authors discuss the importance of mitochondrial DNA mutations in a number of different diseases and speculate how such mutations could lead to cell loss. Increasing our understanding of how mitochondrial DNA mutations affect mitochondrial metabolism and subsequently result in neurodegenerative disease will prove vital to the development of targeted therapies and treatments.
引用
收藏
页码:645 / 658
页数:14
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