Knock-out and transgenic mouse models of tauopathies

被引:87
|
作者
Denk, Franziska [1 ]
Wade-Martins, Richard [1 ]
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
基金
英国惠康基金;
关键词
MAPT; Tau; Tauopathies; Transgenic mouse models; Knock-out mouse model; Alzheimer's disease; Progressive supranuclear palsy; PROGRESSIVE SUPRANUCLEAR PALSY; NEUROFIBRILLARY TANGLE FORMATION; GLYCOGEN-SYNTHASE KINASE-3; PAIRED HELICAL FILAMENTS; MESSENGER-RNA ISOFORMS; TAU-DEFICIENT MICE; R406W HUMAN TAU; V337M HUMAN TAU; P301L HUMAN-TAU; ALZHEIMERS-DISEASE;
D O I
10.1016/j.neurobiolaging.2007.05.010
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Tauopathies, characterized by the dysfunction and aggregation of the microtubule-associated protein tau (MAPT), represent some of the most devastating neurodegenerative disorders afflicting the elderly, including Alzheimers disease and progressive supranuclear palsy. Here we review the range of Mapt knock-out and MAPT transgenic mouse models which have proven successful at providing insights into the molecular mechanisms of neurodegenerative disease. In this overview we highlight several themes, including the insights such models provide into the cellular and molecular mechanisms of tauopathy, the direct relationship between neuropathology and behaviour, and the use of mouse models to help provide a platform for testing novel therapies. Mouse models have helped clarify the relationship between pathological forms of tau, cell death, and the emergence of disease, as well as the interaction between tau and other disease-associated molecules, such as the A beta peptide. Finally, we discuss potential future MAPT genomic DNA models to investigate the importance of alternative splicing of the MAPT locus and its role in sporadic tauopathies. (C) 2007 Elsevier Inc. All rights reserved.
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页码:1 / 13
页数:13
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