Microtubule-associated protein tau in development, degeneration and protection of neurons

被引:335
作者
Wang, Jian-Zhi [1 ]
Liu, Fei [2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Hubei Prov Key Lab Neurol Dis, Dept Pathophysiol, Wuhan 430030, Peoples R China
[2] Nantong Univ, Jiangsu Key Lab Neuroregenerat, Jiangsu 226001, Peoples R China
基金
中国国家自然科学基金;
关键词
microtubule-associated protein; tau; phosphorylation; neurodegeneration;
D O I
10.1016/j.pneurobio.2008.03.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:148 / 175
页数:28
相关论文
共 406 条
[1]   Nonsaturable binding indicates clustering of Tau on the microtubule surface in a paired helical filament-like conformation [J].
Ackmann, M ;
Wiech, H ;
Mandelkow, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (39) :30335-30343
[2]   MAP2 and tau bind longitudinally along the outer ridges of microtubule protofilaments [J].
Al-Bassam, J ;
Ozer, RS ;
Safer, D ;
Halpain, S ;
Milligan, RA .
JOURNAL OF CELL BIOLOGY, 2002, 157 (07) :1187-1196
[3]   HISTOPATHOLOGICAL CRITERIA FOR PROGRESSIVE DEMENTIA DISORDERS - CLINICAL-PATHOLOGICAL CORRELATION AND CLASSIFICATION BY MULTIVARIATE DATA-ANALYSIS [J].
ALAFUZOFF, I ;
IQBAL, K ;
FRIDEN, H ;
ADOLFSSON, R ;
WINBLAD, B .
ACTA NEUROPATHOLOGICA, 1987, 74 (03) :209-225
[4]  
Allen B, 2002, J NEUROSCI, V22, P9340
[5]   Abnormal phosphorylation of tan and the mechanism of Alzheimer neurofibrillary degeneration: Sequestration of microtubule-associated proteins 1 and 2 and the disassembly of microtubules by the abnormal tau [J].
Alonso, AD ;
GrundkeIqbal, I ;
Barra, HS ;
Iqbal, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (01) :298-303
[6]   Alzheimer's disease hyperphosphorylated tau sequesters normal tau into tangles of filaments and disassembles microtubules [J].
Alonso, AD ;
GrundkeIqbal, I ;
Iqbal, K .
NATURE MEDICINE, 1996, 2 (07) :783-787
[7]  
Alonso AD, 2001, J BIOL CHEM, V276, P37967
[8]   ROLE OF ABNORMALLY PHOSPHORYLATED TAN IN THE BREAKDOWN OF MICROTUBULES IN ALZHEIMER-DISEASE [J].
ALONSO, AD ;
ZAIDI, T ;
GRUNDKEIQBAL, I ;
IQBAL, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (12) :5562-5566
[9]   Promotion of hyperphosphorylation by frontotemporal dementia tau mutations [J].
Alonso, AD ;
Mederlyova, A ;
Novak, M ;
Grundke-Iqbal, I ;
Iqbal, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (33) :34873-34881
[10]   Hyperphosphorylation induces self-assembly of τ into tangles of paired helical filaments/straight filaments [J].
Alonso, AD ;
Zaidi, T ;
Novak, M ;
Grundke-Iqbal, I ;
Iqbal, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (12) :6923-6928