Mitochondrial involvement in Alzheimer's disease

被引:126
作者
Bonilla, E
Tanji, K
Hirano, M
Vu, TH
DiMauro, S
Schon, EA
机构
[1] Columbia Univ, Dept Neurol, Coll Phys & Surg, New York, NY 10032 USA
[2] Columbia Univ, Dept Genet & Dev, Coll Phys & Surg, New York, NY 10032 USA
[3] Columbia Univ, Dept Pathol, Coll Phys & Surg, New York, NY 10032 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 1999年 / 1410卷 / 02期
基金
美国国家卫生研究院;
关键词
aging; Alzheimer; deletion; hippocampus; mitochondrion; mitochondrial encephalomyopathy; mtDNA; neuritic plaque; neurofibrillary tangle; neuropathology; oxidative phosphorylation; oxidative stress; point mutation; reactive oxygen species; respiratory chain;
D O I
10.1016/S0005-2728(98)00165-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The causes of most neurodegenerative diseases, including sporadic Alzheimer's disease (AD), remain enigmatic. There is, however, increasing evidence implicating mitochondrial dysfunction resulting from deafferentiation of disconnected neural circuits in the pathogenesis of energy deficit in AD. The patterns of reduced expression of both mitochondrial DNA (mtDNA) and nuclear DNA (nDNA) encoded genes is consistent with a physiological down-regulation of the mitochondrial respiratory chain in response to reduced neuronal activity. On the other hand, the role(s) of somatic cell or maternally inherited mtDNA mutations in the pathogenesis of mitochondrial dysfunction in AD are still controversial. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:171 / 182
页数:12
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