Mitochondria and Cell Bioenergetics: Increasingly Recognized Components and a Possible Etiologic Cause of Alzheimer's Disease

被引:160
作者
Swerdlow, Russell H. [1 ,2 ,3 ]
机构
[1] Univ Kansas, Med Ctr, Sch Med, Landon Ctr Aging,Dept Neurol, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Dept Mol & Integrat Physiol, Kansas City, KS 66160 USA
[3] Univ Kansas, Med Ctr, Dept Biochem & Mol Biol, Kansas City, KS 66160 USA
关键词
CYTOCHROME-C-OXIDASE; AMYLOID PRECURSOR PROTEIN; NF-KAPPA-B; CULTURED SKIN FIBROBLASTS; GENOME-WIDE ASSOCIATION; FACTOR-A TFAM; SYNONYMOUS CODON SUBSTITUTIONS; DEFICIENT HIPPOCAMPAL-NEURONS; MILD COGNITIVE IMPAIRMENT; ELECTRON-TRANSPORT CHAIN;
D O I
10.1089/ars.2011.4149
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
Significance: Mitochondria and brain bioenergetics are increasingly thought to play an important role in Alzheimer's disease (AD). Recent Advances: Data that support this view are discussed from the perspective of the amyloid cascade hypothesis, which assumes beta-amyloid perturbs mitochondrial function, and from an opposite perspective that assumes mitochondrial dysfunction promotes brain amyloidosis. A detailed review of cytoplasmic hybrid (cybrid) studies, which argue mitochondrial DNA (mtDNA) contributes to sporadic AD, is provided. Recent AD endophenotype data that further suggest an mtDNA contribution are also summarized. Critical Issues and Future Directions: Biochemical, molecular, cybrid, biomarker, and clinical data pertinent to the mitochondria-bioenergetics-AD nexus are synthesized and the mitochondrial cascade hypothesis, which represents a mitochondria-centric attempt to conceptualize sporadic AD, is discussed. Antioxid. Redox Signal. 16, 1434-1455.
引用
收藏
页码:1434 / U163
页数:23
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