GSK3: A possible link between beta amyloid peptide and tau protein

被引:241
作者
Hernandez, Felix
Gomez de Barreda, Elena
Fuster-Matanzo, Almudena
Lucas, Jose J. [2 ]
Avila, Jesus [1 ,2 ]
机构
[1] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa, CSIC, E-28049 Madrid, Spain
[2] CIBERNED, Madrid, Spain
关键词
Alzheimer disease; Beta-amyloid peptide; ApoE4; GSK3; Presenilin; Tau; PAIRED HELICAL FILAMENTS; GLYCOGEN-SYNTHASE KINASE-3; ALZHEIMERS-DISEASE; TRANSGENIC MICE; ABNORMAL PHOSPHORYLATION; SIGNAL-TRANSDUCTION; FIBRILLAR POLYMERS; APOLIPOPROTEIN-E; MOUSE MODEL; A-BETA;
D O I
10.1016/j.expneurol.2009.09.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tau is a neuronal microtubule-associated phosphoprotein that is highly phosphorylated by glycogen synthase kinase 3 (GSK3). Tau phosphorylation by GSK3 regulates tau binding to microtubules, tau degradation and tau aggregation. Tau phosphorylation is important in Alzheimer disease pathology and in other tauopathies. In Alzheimer disease, it has been proposed that the peptide beta amyloid promotes GSK3 activation, resulting in tau phosphorylation. In this work, we review the links between beta amyloid peptide, tau protein and GSK3 that occur in familial Alzheimer disease. We also discuss the possible links between GSK3 and sporadic Alzheimer disease. Finally, we include a brief review of the pathology of animal models overexpressing GSK3. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:322 / 325
页数:4
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