Tau as a therapeutic target in neurodegenerative disease

被引:100
作者
Himmelstein, Diana S. [1 ]
Ward, Sarah M. [1 ]
Lancia, Jody K. [1 ]
Patterson, Kristina R. [1 ]
Binder, Lester I. [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Cell & Mol Biol, Chicago, IL 60611 USA
关键词
Alzheimer's disease; Tauopathy; Phosphorylation effectors; Immunotherapy; Aggregation inhibitors; Microtubule stabilization; PAIRED HELICAL FILAMENTS; MICROTUBULE-ASSOCIATED PROTEIN; GLYCOGEN-SYNTHASE KINASE-3-BETA; DEPENDENT AXONAL-TRANSPORT; PROLYL ISOMERASE PIN1; 3RD REPEAT FRAGMENTS; ALZHEIMERS-DISEASE; IN-VITRO; MOUSE MODEL; NEUROFIBRILLARY TANGLES;
D O I
10.1016/j.pharmthera.2012.07.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tau is a microtubule-associated protein thought to help modulate the stability of neuronal microtubules. In tauopathies, including Alzheimer's disease and several frontotemporal dementias, tau is abnormally modified and misfolded resulting in its disassociation from microtubules and the generation of pathological lesions characteristic for each disease. A recent surge in the population of people with neurodegenerative tauopathies has highlighted the immense need for disease-modifying therapies for these conditions, and new attention has focused on tau as a potential target for intervention. In the current work we summarize evidence linking tau to disease pathogenesis and review recent therapeutic approaches aimed at ameliorating tau dysfunction. The primary therapeutic tactics considered include kinase inhibitors and phosphatase activators, immunotherapies, small molecule inhibitors of protein aggregation, and microtubule-stabilizing agents. Although the evidence for tau-based treatments is encouraging, additional work is undoubtedly needed to optimize each treatment strategy for the successful development of safe and effective therapeutics. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:8 / 22
页数:15
相关论文
共 161 条
[1]  
Abraha A, 2000, J CELL SCI, V113, P3737
[2]  
Allen B, 2002, J NEUROSCI, V22, P9340
[3]   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
[4]   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
[5]   Cell-cycle reentry and cell death in transgenic mice expressing nonmutant human tau isoforms [J].
Andorfer, C ;
Acker, CM ;
Kress, Y ;
Hof, PR ;
Duff, K ;
Davies, P .
JOURNAL OF NEUROSCIENCE, 2005, 25 (22) :5446-5454
[6]   Hyperphosphorylation and aggregation of tau in mice expressing normal human tau isoforms [J].
Andorfer, C ;
Kress, Y ;
Espinoza, M ;
de Silva, R ;
Tucker, KL ;
Barde, YA ;
Duff, K ;
Davies, P .
JOURNAL OF NEUROCHEMISTRY, 2003, 86 (03) :582-590
[7]   NEUROFIBRILLARY TANGLES BUT NOT SENILE PLAQUES PARALLEL DURATION AND SEVERITY OF ALZHEIMERS-DISEASE [J].
ARRIAGADA, PV ;
GROWDON, JH ;
HEDLEYWHYTE, ET ;
HYMAN, BT .
NEUROLOGY, 1992, 42 (03) :631-639
[8]   TAU, THE NEURONAL HEAT-STABLE MICROTUBULE-ASSOCIATED PROTEIN, IS ALSO PRESENT IN THE CROSS-LINKED MICROTUBULE NETWORK OF THE TESTICULAR SPERMATID MANCHETTE [J].
ASHMAN, JB ;
HALL, ES ;
EVELETH, J ;
BOEKELHEIDE, K .
BIOLOGY OF REPRODUCTION, 1992, 46 (01) :120-129
[9]   Immunotherapy targeting pathological tau conformers in a tangle mouse model reduces brain pathology with associated functional improvements [J].
Asuni, Ayodeji A. ;
Boutajangout, Allal ;
Quartermain, David ;
Sigurdsson, Einar M. .
JOURNAL OF NEUROSCIENCE, 2007, 27 (34) :9115-9129
[10]   Pin1 inhibition activates cyclin D and produces neurodegenerative pathology [J].
Atabay, Kutay Deniz ;
Karabay, Arzu .
JOURNAL OF NEUROCHEMISTRY, 2012, 120 (03) :430-439