Amyloid-β oligomers:: their production, toxicity and therapeutic inhibition

被引:426
作者
Walsh, DM [1 ]
Klyubin, I
Fadeeva, JV
Rowan, MJ
Selkoe, DJ
机构
[1] Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Ctr Neurol Dis, Boston, MA 02115 USA
[3] Univ Dublin Trinity Coll, Dept Pharmacol & Therapeut, Dublin 2, Ireland
关键词
Alzheimer's disease; amyloid beta-protein; long-term protentiation; neurotoxicity; oligomerization;
D O I
10.1042/BST0300552
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
Despite extensive genetic and animal modelling data that support a central role for the amyloid beta-protein (Abeta) in the genesis of Alzheimer's disease, the specific form(s) of Abeta which causes injury to neurons in vivo has not been identified. In the present study, we examine the importance of soluble, pre-fibrillar assemblies of Abeta as mediators of neurotoxicity. Specifically, we review the role of cell-derived SDS-stable oligomers, their blocking of hippocampal long-term potentiation in vivo and the finding that this blocking can be prevented by prior treatment of oligomer-producing cells with gamma-secretase inhibitors.
引用
收藏
页码:552 / 557
页数:6
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