The GSK3 hypothesis of Alzheimer's disease

被引:1006
作者
Hooper, Claudie [1 ]
Killick, Richard [1 ]
Lovestone, Simon [1 ]
机构
[1] Kings Coll London, MRC Ctr Neurodegenerat Res, Inst Psychiat, London WC2R 2LS, England
关键词
Wnt; insulin; tau; beta-amyloid; memory; inflammation;
D O I
10.1111/j.1471-4159.2007.05194.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Glycogen synthase kinase 3 (GSK3) is a constitutively active, proline-directed serine/threonine kinase that plays a part in a number of physiological processes ranging from glycogen metabolism to gene transcription. GSK3 also plays a pivotal and central role in the pathogenesis of both sporadic and familial forms of Alzheimer's disease (AD), an observation that has led us to coin the 'GSK3 hypothesis of AD'. According to this hypothesis, over-activity of GSK3 accounts for memory impairment, tau hyper-phosphorylation, increased beta-amyloid production and local plaque-associated microglial-mediated inflammatory responses; all of which are hallmark characteristics of AD. If our 'GSK3 hypothesis of AD' is substantiated and GSK3 is indeed a causal mediator of AD then inhibitors of GSK3 would provide a novel avenue for therapeutic intervention in this devastating disorder.
引用
收藏
页码:1433 / 1439
页数:7
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