Up-regulation of calcineurin Aβ mRNA in the Alzheimer's disease brain:: Assessment by cDNA microarray

被引:97
作者
Hata, R [1 ]
Masumura, M
Akatsu, H
Li, F
Fujita, H
Nagai, Y
Yamamoto, T
Okada, H
Kosaka, K
Sakanaka, M
Sawada, T
机构
[1] Ehime Univ, Sch Med, Dept Anat & Neurosci, Shigenobu, Ehime 7910295, Japan
[2] Natl Cardiovasc Ctr, BF Res Inst, Suita, Osaka 5650873, Japan
[3] Fukushimura Hosp, Choju Med Inst, Toyohashi, Aichi 4418124, Japan
[4] Nagoya City Univ, Sch Med, Dept Mol Biol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[5] Yokohama City Univ, Sch Med, Dept Psychiat, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
关键词
Alzheimer's disease; microarray; calcineurin; neurofibrillary tangle; senile plaque;
D O I
10.1006/bbrc.2001.4968
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
Recent advances in cDNA microarray technology have made it possible to analyze expression of more than 8000 genes. Using this technology, gene expression in the hippocampus containing neurofibrillary tangle-associated lesions from an Alzheimer's disease (AD) patient was compared with expression in the parietal;cortex from the same patient that lacked these lesions. We also compared gene expression using a control brain. The top 20 named genes significantly up-regulated or down-regulated only in the AD brain were determined. The most up-regulated gene proved to be calcineurin A beta mRNA (CA beta). In situ hybridization histochemistry revealed that CA beta was significantly up-regulated in pyramidal neurons of the hippocampus in the AD brain. RT-PCR analysis revealed that CA beta was up-regulated in the hippocampus from two out of three AD brains while there were no changes in three control brains. Our study suggests that CA beta may play a crucial role in the pathophysiological mechanisms in AD. (C) 2001 Academic Press.
引用
收藏
页码:310 / 316
页数:7
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