Tau phosphorylation: the therapeutic challenge for neurodegenerative disease

被引:687
|
作者
Hanger, Diane P. [1 ]
Anderton, Brian H. [1 ]
Noble, Wendy [1 ]
机构
[1] Kings Coll London, Inst Psychiat, Ctr Neurodegenerat Res, MRC, London SE5 8AF, England
基金
英国医学研究理事会;
关键词
CYCLIN-DEPENDENT KINASE-5; HELICAL FILAMENT-TAU; N-TERMINAL KINASE; ALZHEIMERS-DISEASE; PROTEIN-TAU; FETAL-TAU; TYROSINE PHOSPHORYLATION; RECOMBINANT TAU; CELL MODELS; C-ABL;
D O I
10.1016/j.molmed.2009.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The microtubule-associated protein tau is integral to the pathogenesis of Alzheimer's disease (AD), as well as several related disorders, termed tauopathies, in which tau is deposited in affected brain regions. In the tauopathies, pathological tau is in an elevated state of phosphorylation and is alberrantly cleaved. It also exhibits abnormal conformations and becomes aggregated, resulting in neurofibrillary tau pathology. Recent evidence suggests that relatively early disease-associated changes in soluble tau proteins, including phosphorylation, are involved in the induction of neuronal death. Here, we summarize recent developments that suggest new therapeutic strategies to prevent or reduce the progression of pathology in the tauopathies. A list of tau phosphorylation sites identified in the tauopathies and in controls accompanies this review.
引用
收藏
页码:112 / 119
页数:8
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