Tau and neurodegenerative disease: the story so far

被引:559
作者
Iqbal, Khalid [1 ]
Liu, Fei [1 ]
Gong, Cheng-Xin [1 ]
机构
[1] New York State Inst Basic Res Dev Disabil, Dept Neurochem, Staten Isl, NY 10314 USA
关键词
MICROTUBULE-ASSOCIATED-PROTEIN; PAIRED HELICAL FILAMENTS; ALZHEIMER NEUROFIBRILLARY TANGLES; ABNORMALLY PHOSPHORYLATED-TAU; PHOSPHOPROTEIN PHOSPHATASE 2A; CYCLIN-DEPENDENT KINASE-5; GLYCOGEN-SYNTHASE KINASE-3; MULTIPLE SYSTEM TAUOPATHY; BRAIN GLUCOSE-METABOLISM; IN-VITRO PHOSPHORYLATION;
D O I
10.1038/nrneurol.2015.225
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In 1975, tau protein was isolated as a microtubule-associated factor from the porcine brain. In the previous year, a paired helical filament (PHF) protein had been identified in neurofibrillary tangles in the brains of individuals with Alzheimer disease (AD), but it was not until 1986 that the PHF protein and tau were discovered to be one and the same. In the AD brain, tau was found to be abnormally hyperphosphorylated, and it inhibited rather than promoted in vitro microtubule assembly. Almost 80 disease-causing exonic missense and intronic silent mutations in the tau gene have been found in familial cases of frontotemporal dementia but, to date, no such mutation has been found in AD. The first phase I clinical trial of an active tau immunization vaccine in patients with AD was recently completed. Assays for tau levels in cerebrospinal fluid and plasma are now available, and tau radiotracers for PET are under development. In this article, we provide an overview of the pivotal discoveries in the tau research field over the past 40 years. We also review the current status of the field, including disease mechanisms and therapeutic approaches.
引用
收藏
页码:15 / 27
页数:13
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