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利用转基因小鼠分析tau蛋白病

Analysis of tauopathies with transgenic mice.

作者信息

Hutton M, Lewis J, Dickson D, Yen S H, McGowan E

机构信息

Department of Neuroscience, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, USA.

出版信息

Trends Mol Med. 2001 Oct;7(10):467-70. doi: 10.1016/s1471-4914(01)02123-2.

Abstract

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.

摘要

由微管相关蛋白tau组成的神经元内丝状内含物是几种神经退行性疾病(包括阿尔茨海默病)的特征,这些疾病被称为tau蛋白病。一个关键发现是在1998年鉴定出与17号染色体连锁的额颞叶痴呆伴帕金森综合征相关的tau基因突变。这表明tau功能障碍足以导致神经退行性变,并表明tau可能在其他tau蛋白病的发病机制中起关键作用。然而,tau丝状病变形成的机制及其在神经退行性变中的作用仍不确定。人类tau蛋白病转基因小鼠模型开发的最新进展使这些问题得以解决。

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