共 28 条
Analysis of tauopathies with transgenic mice
被引:71
作者:

Hutton, M
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机构:
Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA

Lewis, J
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机构:
Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA

Dickson, D
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机构:
Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA

Yen, SH
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机构:
Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA

McGowan, E
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机构:
Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA
机构:
[1] Mayo Clin Jacksonville, Dept Neurosci, Jacksonville, FL 32224 USA
关键词:
D O I:
10.1016/S1471-4914(01)02123-2
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:
Intraneuronal filamentous inclusions composed of the microtubule-associated protein tau are a feature of several neurodegenerative diseases (including Alzheimer's disease) known as tauopathies. A pivotal finding was the identification in 1998 of mutations in tau associated with frontotemporal dementia with parkinsonism linked to chromosome 17. This demonstrated that tau dysfunction is sufficient to cause neurodegeneration, and indicated that tau is likely to play a crucial role in the pathogenesis of other tauopathies. However, the mechanism by which tau filamentous lesions form and their role in neurodegeneration remains uncertain. Recent progress in the development of transgenic mouse models of human tauopathy is allowing these questions to be addressed.
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页码:467 / 470
页数:4
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