The Alzheimer's disease mitochondrial cascade hypothesis: An update

被引:177
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
相关论文
共 136 条
[1]   Frequent Amyloid Deposition Without Significant Cognitive Impairment Among the Elderly [J].
Aizenstein, Howard Jay ;
Nebes, Robert D. ;
Saxton, Judith A. ;
Price, Julie C. ;
Mathis, Chester A. ;
Tsopelas, Nicholas D. ;
Ziolko, Scott K. ;
James, Jeffrey A. ;
Snitz, Beth E. ;
Houck, Patricia R. ;
Bi, Wenzhu ;
Cohen, Ann D. ;
Lopresti, Brian J. ;
DeKosky, Steven T. ;
Halligan, Edythe M. ;
Klunk, William E. .
ARCHIVES OF NEUROLOGY, 2008, 65 (11) :1509-1517
[2]  
Alvarez V, 2008, J ALZHEIMERS DIS, V13, P275
[3]   Amyloid precursor protein and mitochondrial dysfunction in Alzheimer's disease [J].
Anandatheerthavarada, Hindupur K. ;
Devi, Latha .
NEUROSCIENTIST, 2007, 13 (06) :626-638
[4]   Mitochondrial targeting and a novel transmembrane arrest of Alzheimer's amyloid precursor protein impairs mitochondrial function in neuronal cells [J].
Anandatheerthavarada, HK ;
Biswas, G ;
Robin, MA ;
Avadhani, NG .
JOURNAL OF CELL BIOLOGY, 2003, 161 (01) :41-54
[5]  
[Anonymous], 1968, AMYLOIDOSIS
[6]  
Arendt T, 2000, ANN NY ACAD SCI, V920, P249
[7]   Reversible paired helical filament-like phosphorylation of tau is an adaptive process associated with neuronal plasticity in hibernating animals [J].
Arendt, T ;
Stieler, J ;
Strijkstra, AM ;
Hut, RA ;
Rüdiger, J ;
Van der Zee, EA ;
Harkany, T ;
Holzer, M ;
Härtig, W .
JOURNAL OF NEUROSCIENCE, 2003, 23 (18) :6972-6981
[8]   Association of an extended haplotype in the tau gene with progressive supranuclear palsy [J].
Baker, M ;
Litvan, I ;
Houlden, H ;
Adamson, J ;
Dickson, D ;
Perez-Tur, J ;
Hardy, J ;
Lynch, T ;
Bigio, E ;
Hutton, M .
HUMAN MOLECULAR GENETICS, 1999, 8 (04) :711-715
[9]  
Baloyannis SJ, 2006, J ALZHEIMERS DIS, V9, P119
[10]   Reduced steady-state levels of mitochondrial RNA and increased mitochondrial DNA amount in human brain with aging [J].
Barrientos, A ;
Casademont, J ;
Cardellach, F ;
Estivill, X ;
Urbano-Marquez, A ;
Nunes, V .
MOLECULAR BRAIN RESEARCH, 1997, 52 (02) :284-289