High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

被引:1164
作者
Bender, A
Krishnan, KJ
Morris, CM
Taylor, GA
Reeve, AK
Perry, RH
Jaros, E
Hersheson, JS
Betts, J
Klopstock, T
Taylor, RW
Turnbull, DM [1 ]
机构
[1] Univ Newcastle Upon Tyne, Sch Med, Mitochondrial Res Grp, Sch Neurol Neurobiol & Psychiat, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Newcastle Gen Hosp, Inst Ageing & Hlth, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[3] Newcastle Gen Hosp, Dept Neuropathol, Inst Hlth Elderly, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[4] Univ Munich, Klinikum Grosshadern, Dept Neurol, D-81377 Munich, Germany
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1038/ng1769
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Here we show that in substantia nigra neurons from both aged controls and individuals with Parkinson disease, there is a high level of deleted mitochondrial DNA (mtDNA) (controls, 43.3% +/- 9.3%; individuals with Parkinson disease, 52.3% +/- 9.3%). These mtDNA mutations are somatic, with different clonally expanded deletions in individual cells, and high levels of these mutations are associated with respiratory chain deficiency. Our studies suggest that somatic mtDNA deletions are important in the selective neuronal loss observed in brain aging and in Parkinson disease.
引用
收藏
页码:515 / 517
页数:3
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