Role of GSK-3β in Alzheimer's disease pathology

被引:72
作者
Planel, E [1 ]
Sun, XY [1 ]
Takashima, A [1 ]
机构
[1] Brain Sci Inst, Lab Alzheimers Dis, Wako, Saitama 3510198, Japan
关键词
GSK-3; beta; tau; APP; kinesin; amyloid-beta; insulin; neurofibrillary tangles; phosphatase; pro-apoptosis;
D O I
10.1002/ddr.10100
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glycogen synthase kinase 3beta (GSK-3beta) is an important regulatory kinase involved in multiple processes such as metabolic control, embryonic development, cell death, and oncogenesis. It has been found to interact with many molecules associated with Alzheimer's disease (AD) such as the microtubule-associated protein tau, presenilin 1, the amyloid-beta peptide, the amyloid precursor protein, and acetylcholine. Furthermore, GSK-3beta might be involved in brain aging and longevity. As GSK-3beta is associated with so many components of AD pathology, we review the current data on the role of this kinase in tau hyperphosphorylation, then look at its association with AD-related molecules and pathways, and finally discuss its involvement in cell death and aging. We attempt to integrate all these data to arrive at the proposition that GSK-3beta is a pivotal molecule in the evolution of AD and that developing drugs directed at this kinase might prove to be beneficial in the treatment of this devastating disease.
引用
收藏
页码:491 / 510
页数:20
相关论文
共 233 条
[81]   DIFFERENT LOCALIZATION OF TAU-PROTEIN-KINASE-I GLYCOGEN-SYNTHASE KINASE-3-BETA FROM GLYCOGEN-SYNTHASE KINASE-3-ALPHA IN CEREBELLUM MITOCHONDRIA [J].
HOSHI, M ;
SATO, M ;
KONDO, S ;
TAKASHIMA, A ;
NOGUCHI, K ;
TAKAHASHI, M ;
ISHIGURO, K ;
IMAHORI, K .
JOURNAL OF BIOCHEMISTRY, 1995, 118 (04) :683-685
[82]   Regulation of mitochondrial pyruvate dehydrogenase activity by tau protein kinase 1 glycogen synthase kinase 3 beta in brain [J].
Hoshi, M ;
Takashima, A ;
Noguchi, K ;
Murayama, M ;
Sato, M ;
Kondo, S ;
Saitoh, Y ;
Ishiguro, K ;
Hoshino, T ;
Imahori, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) :2719-2723
[83]   Brain glucose and energy metabolism abnormalities in sporadic Alzheimer disease. Causes and consequences: an update [J].
Hoyer, S .
EXPERIMENTAL GERONTOLOGY, 2000, 35 (9-10) :1363-1372
[84]   MODULATION OF THE GLYCOGEN-SYNTHASE KINASE-3 FAMILY BY TYROSINE PHOSPHORYLATION [J].
HUGHES, K ;
NIKOLAKAKI, E ;
PLYTE, SE ;
TOTTY, NF ;
WOODGETT, JR .
EMBO JOURNAL, 1993, 12 (02) :803-808
[85]   Activation of phospholipase C-gamma by the concerted action of tau proteins and arachidonic acid [J].
Hwang, SC ;
Jhon, DY ;
Bae, YS ;
Kim, JH ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (31) :18342-18349
[86]   The endogenous and cell cycle-dependent phosphorylation of tau protein in living cells:: Implications for Alzheimer's disease [J].
Illenberger, S ;
Zheng-Fischhöfer, QY ;
Preuss, U ;
Stamer, K ;
Baumann, K ;
Trinczek, B ;
Biernat, J ;
Godemann, R ;
Mandelkow, EM ;
Mandelkow, E .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (06) :1495-1512
[87]  
Imahori K, 1997, J BIOCHEM, V121, P179
[88]   Microtubule-associated protein tau in human fibroblasts with the Swedish Alzheimer mutation [J].
Ingelson, M ;
Vanmechelen, E ;
Lannfelt, L .
NEUROSCIENCE LETTERS, 1996, 220 (01) :9-12
[89]   Dual effects of PKNα and protein kinase C on phosphorylation of tau protein by glycogen synthase kinase-3β [J].
Isagawa, T ;
Mukai, H ;
Oishi, K ;
Taniguchi, T ;
Hasegawa, H ;
Kawamata, T ;
Tanaka, C ;
Ono, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (01) :209-212
[90]   A NOVEL TUBULIN-DEPENDENT PROTEIN-KINASE FORMING A PAIRED HELICAL FILAMENT EPITOPE ON TAU [J].
ISHIGURO, K ;
IHARA, Y ;
UCHIDA, T ;
IMAHORI, K .
JOURNAL OF BIOCHEMISTRY, 1988, 104 (03) :319-321