Higuchi Makoto, Lee Virginia M Y, Trojanowski John Q
Neuromolecular Med. 2002;2(2):131-50. doi: 10.1385/NMM:2:2:131.
The microtubule (MT)-associated protein (MAP) tau in neurons has been implicated as a significant factor in the axonal growth, development of neuronal polarity, and the maintenance of MT dynamics. Tau is localized to the axon, and is known to promote MT assembly and to stabilize axonal MTs. These functions of tau are primarily regulated by the activities of protein kinases and phosphatases. In Alzheimer's disease and other neurodegenerative disorders, abundant filamentous tau inclusions are found to be major neuropathological characteristics of these diseases. Both somato-dendritic and axonal tau lesions appear to be closely associated with axonal disruption. Furthermore, recent discoveries of pathogenic mutations on the tau gene suggest that abnormalities of tau alone are causative of neurodegeneration. Finally, analyses of transgenic mice that express human tau proteins have enabled in vivo quantitative assessments of axonal functions and have provided information about mechanistic relationships between pathological alteration of tau and axonal degeneration.
神经元中的微管(MT)相关蛋白(MAP)tau被认为是轴突生长、神经元极性发育以及微管动力学维持的重要因素。Tau定位于轴突,已知其能促进微管组装并稳定轴突微管。Tau的这些功能主要受蛋白激酶和磷酸酶活性的调节。在阿尔茨海默病和其他神经退行性疾病中,大量丝状tau包涵体是这些疾病的主要神经病理学特征。体细胞-树突状和轴突tau病变似乎都与轴突破坏密切相关。此外,最近在tau基因上发现的致病突变表明,仅tau异常就可导致神经退行性变。最后,对表达人类tau蛋白的转基因小鼠的分析实现了对轴突功能的体内定量评估,并提供了有关tau病理改变与轴突变性之间机制关系信息。