Wang Jian-Zhi, Liu Fei
Pathophysiology Department, Hubei Provincial Key Laboratory of Neurological Diseases, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, PR China.
Prog Neurobiol. 2008 Jun;85(2):148-75. doi: 10.1016/j.pneurobio.2008.03.002. Epub 2008 Mar 22.
As a principal neuronal microtubule-associated protein, tau has been recognized to play major roles in promoting microtubule assembly and stabilizing the microtubules and to maintain the normal morphology of the neurons. Recent studies suggest that tau, upon alternative mRNA splicing and multiple posttranslational modifications, may participate in the regulations of intracellular signal transduction, development and viability of the neurons. Furthermore, tau gene mutations, aberrant mRNA splicing and abnormal posttranslational modifications, such as hyperphosphorylation, have also been found in a number of neurodegenerative disorders, collectively known as tauopathies. Therefore, changes in expression of the tau gene, alternative splicing of its mRNA and its posttranslational modification can modulate the normal architecture and functions of neurons as well as in a situation of tauopathies, such as Alzheimer's disease. The primary aim of this review is to summarize the latest developments and perspectives in our understanding about the roles of tau, especially hyperphosphorylation, in the development, degeneration and protection of neurons.
作为一种主要的神经元微管相关蛋白,tau蛋白被认为在促进微管组装、稳定微管以及维持神经元的正常形态方面发挥着重要作用。最近的研究表明,tau蛋白在经历可变mRNA剪接和多种翻译后修饰后,可能参与细胞内信号转导、神经元发育和生存能力的调控。此外,在许多神经退行性疾病(统称为tau蛋白病)中也发现了tau基因突变、异常的mRNA剪接和异常的翻译后修饰,如过度磷酸化。因此,tau基因表达的变化、其mRNA的可变剪接及其翻译后修饰,既能调节神经元的正常结构和功能,也能在tau蛋白病(如阿尔茨海默病)的情况下发挥作用。本综述的主要目的是总结我们对tau蛋白,尤其是过度磷酸化在神经元发育、退化和保护中的作用的最新认识进展和观点。