Soluble Aß oligomer production and toxicity

被引:337
作者
Larson, Megan E. [2 ,3 ]
Lesne, Sylvain E. [1 ,2 ,3 ]
机构
[1] Univ Minnesota, Dept Neurosci, Inst Translat Neurosci Scholar, Minneapolis, MN 55414 USA
[2] Univ Minnesota, N Bud Grossman Ctr Memory Res & Care, Minneapolis, MN 55414 USA
[3] Univ Minnesota, Inst Translat Neurosci, Minneapolis, MN 55414 USA
关键词
Alzheimer's disease; amyloid-beta; oligomer; transgenic mouse; AMYLOID-BETA-PROTEIN; CELLULAR PRION PROTEIN; LONG-TERM POTENTIATION; TRANSGENIC MOUSE MODEL; ALZHEIMERS-DISEASE; SYNAPTIC PLASTICITY; IN-VIVO; LIPID RAFTS; COGNITIVE IMPAIRMENTS; TAU PHOSPHORYLATION;
D O I
10.1111/j.1471-4159.2011.07478.x
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
For nearly 100 years following the first description of this neurological disorder by Dr Alois Alzheimer, amyloid plaques and neurofibrillary tangles have been hypothesized to cause neuronal loss. With evidence that the extent of insoluble, deposited amyloid poorly correlated with cognitive impairment, research efforts focused on soluble forms of A beta, also referred as A beta oligomers. Following a decade of studies, soluble oligomeric forms of A beta are now believed to induce the deleterious cascade(s) involved in the pathophysiology of Alzheimers disease. In this review, we will discuss our current understanding about endogenous oligomeric A beta production, their relative toxicity in vivo and in vitro, and explore the potential future directions needed for the field.
引用
收藏
页码:125 / 139
页数:15
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