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微管相关tau蛋白异常磷酸化及磷酸化靶向抑制的研究进展

[Research progress of abnormal phosphorylation of microtubule-associated tau protein and of the targeted inhibition of the phosphorylation].

作者信息

Zhou Futao, Chen Shuangrong, Sun Xuechuan

机构信息

School of Physical Education, Nanchang Hangkong University, Nanchang 330063, China.

出版信息

Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2012 Aug;29(4):788-92.

Abstract

Progressive dementia is described as the first and most prominent symptom of Alzheimer's disease (AD), and hyperphosphorylation of microtubule associated Tau protein (MAPT) plays a key role in neurodegeneration and neuronal dysfunction in AD and other neurodegenerative diseases. This paper reviews several protein kinases and phosphatases which can phosphorylate/dephosphorylate Tau protein, and evaluates a therapeutic strategy based on targeted inhibition of Tau kinases and activation of Tau phosphatases.

摘要

进行性痴呆被描述为阿尔茨海默病(AD)的首要且最突出的症状,微管相关Tau蛋白(MAPT)的过度磷酸化在AD及其他神经退行性疾病的神经变性和神经元功能障碍中起关键作用。本文综述了几种可使Tau蛋白磷酸化/去磷酸化的蛋白激酶和磷酸酶,并评估了基于靶向抑制Tau激酶和激活Tau磷酸酶的治疗策略。

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