Increased levels of granular tau oligomers: An early sign of brain aging and Alzheimer's disease

被引:241
作者
Maeda, S
Sahara, N
Saito, Y
Murayama, S
Ikai, A
Takashima, A
机构
[1] RIKEN, Brain Sci Inst, Lab Alzheimers Dis, Wako, Saitama 3510198, Japan
[2] Tokyo Inst Technol, Dept Life Sci, Grad Sch Biosci & Biotechnol, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[3] Tokyo Metropolitan Inst Gerontol, Dept Neuropathol, Itabashi Ku, Tokyo 1730015, Japan
关键词
Alzheimer's disease (AD); Tau; atomic force microscopy (AFM); Granular tau oligomer; Braak stage; brain aging;
D O I
10.1016/j.neures.2005.11.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Development of Deurofibrillary tangles (NFTs) is a pathological hallmark in various neurodegenerative disorders including Alzheimer's disease (AD). Recently, we identified a granular tau oligomer having a pre-filamentous structure. To determine the role of this oligomer in NFT formation, we quantified the amount of granular tau oligomer in 21 frontal cortex samples, each displaying varying degrees of Braak-staged NFF pathology. Here we report that granular tau oligomer levels in frontal cortex were significantly increased, even in brains displaying Braak-stage I neuropathology, a stage at which clinical symptoms of AD and NFTs in frontal cortex are believed to be absent. This suggests that increases in granular tau oligomer levels occur before NFTs form and before individuals manifest clinical symptoms of AD. Increased granular tau oligomer levels, therefore, may lead to NFT formation in frontal cortex, eventually leading to the development of AD. Thus, increases in granular tau oligomer levels may represent a very early sign of NFT formation and AD. (c) 2005 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:197 / 201
页数:5
相关论文
共 23 条
[1]   Frequency of stages of Alzheimer-related lesions in different age categories [J].
Braak, H ;
Braak, E .
NEUROBIOLOGY OF AGING, 1997, 18 (04) :351-357
[2]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[3]   Neuronal loss correlates with but exceeds neurofibrillary tangles in Alzheimer's disease [J].
GomezIsla, T ;
Hollister, R ;
West, H ;
Mui, S ;
Growdon, JH ;
Petersen, RC ;
Parisi, JE ;
Hyman, BT .
ANNALS OF NEUROLOGY, 1997, 41 (01) :17-24
[4]   A PREPARATION OF ALZHEIMER PAIRED HELICAL FILAMENTS THAT DISPLAYS DISTINCT TAU-PROTEINS BY POLYACRYLAMIDE-GEL ELECTROPHORESIS [J].
GREENBERG, SG ;
DAVIES, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (15) :5827-5831
[5]   APPLICATIONS FOR ATOMIC-FORCE MICROSCOPY OF DNA [J].
HANSMA, HG ;
LANEY, DE ;
BEZANILLA, M ;
SINSHEIMER, RL ;
HANSMA, PK .
BIOPHYSICAL JOURNAL, 1995, 68 (05) :1672-1677
[6]   ANTIBODIES TO PAIRED HELICAL FILAMENTS IN ALZHEIMERS-DISEASE DO NOT RECOGNIZE NORMAL BRAIN PROTEINS [J].
IHARA, Y ;
ABRAHAM, C ;
SELKOE, DJ .
NATURE, 1983, 304 (5928) :727-730
[7]   PHF and PHF-like fibrils - cause or consequence? [J].
Ihara, Y .
NEUROBIOLOGY OF AGING, 2001, 22 (01) :123-126
[8]   Hierarchical phosphorylation of recombinant tau by the paired-helical filament-associated protein kinase is dependent on cyclic AMP-dependent protein kinase [J].
Jicha, GA ;
O'Donnell, A ;
Weaver, C ;
Angeletti, R ;
Davies, P .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (01) :214-224
[9]   Independent accumulations of tau and amyloid β-protein in the human entorhinal cortex [J].
Katsuno, T ;
Morishima-Kawashima, M ;
Saito, Y ;
Yamanouchi, H ;
Ishiura, S ;
Murayama, S ;
Ihara, Y .
NEUROLOGY, 2005, 64 (04) :687-692
[10]   Neurodegenerative tauopathies [J].
Lee, VMY ;
Goedert, M ;
Trojanowski, JQ .
ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 :1121-1159