The Alzheimer's disease mitochondrial cascade hypothesis: An update

被引:170
|
作者
Swerdlow, Russell H. [1 ,2 ]
Khan, Shaharyar M. [3 ]
机构
[1] Univ Kansas, Landon Ctr Aging, Dept Neurol, Sch Med, Kansas City, KS 66160 USA
[2] Univ Kansas, Dept Mol & Integrat Physiol, Sch Med, Kansas City, KS 66160 USA
[3] Gencia Corp, Charlottesville, VA USA
关键词
Alzheimer's disease; Mitochondria; Mitochondrial cascade hypothesis; Cybrids; AMYLOID PRECURSOR PROTEIN; CYTOCHROME-C-OXIDASE; FACTOR-A TFAM; OXIDATIVE DAMAGE; CELL-CYCLE; NEURODEGENERATIVE DISORDERS; TRANSCRIPTION-FACTOR; PARKINSONS-DISEASE; APOLIPOPROTEIN-E; DNA MUTATIONS;
D O I
10.1016/j.expneurol.2009.01.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In 2004 we proposed the mitochondrial cascade hypothesis of sporadic Alzheimer's disease (AD) Our. hypothesis assumed sporadic and autosomal dominant AD are not etiologically homogeneous considered, evidence that AD pathology is not brain-limited, and incorporated aging theory. The mitochondrial cascade hypothesis asserted: (1) inheritance determines mitochondrial baseline function and durability; (2) mitochondrial durability influences how mitochondria change with age; and (3) when mitochondrial change reaches a threshold, AD histopathology and symptoms ensue. We now review the reasoning used to formulate the hypothesis, discuss pertinent interim data, and update its tenants. Readers are invited to consider the conceptual strengths and weaknesses of this hypothesis. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:308 / 315
页数:8
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