Reduced expression of amyloid precursor protein, presenilin-1 and rab3a in cortical brain regions in Alzheimer's disease

被引:24
作者
Davidsson, P [1 ]
Bogdanovic, N
Lannfelt, L
Blennow, K
机构
[1] Univ Gothenburg, Expt Neurosci Sect, Dept Clin Neurosci, SE-43180 Molndal, Sweden
[2] Huddinge Hosp, KFC Novum, Geriatr Sect, Dept Clin Neurosci & Family Med, S-14186 Huddinge, Sweden
关键词
amyloid precursor protein; Alzheimer's disease; cortical brain regions; immunoblotting; presenilin-1; rab3a;
D O I
10.1159/000051266
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
To study the role of amyloid precursor protein (APP) in the pathogenesis of Alzheimer's disease (AD), the level of APP was analysed by quantitative immunoblotting in 6 AD patients and 6 age-matched controls in 9 brain regions. These were associative cortices (orbital frontal cortex, inferior temporal cortex, inferior parietal cortex), primary cortex (occipital cortex), limbic structures (anterior cingulate gyrus, hippocampus), subcortical structures (putamen, thalamus) and cerebellum. To assess a potential relationship between APP and presenilin-1 (PS-1) and/or synaptic proteins, the levels of PS-1 and rab3a, a specific synaptic vesicle protein, were also determined in the same tissue samples. The level of APP was almost the same in the association cortical regions, primary cortex, and limbic structures and in the subcortical structures, while the lowest level was found in the cerebellum. There were more marked differences in the level of PS-1 and rab3a between different brain regions. The highest levels of PS-1 and rab3a were found in the association cortical areas, while intermediate levels were found in primary cortex, limbic structures and subcortical structures. As for APP, the lowest level was found in cerebellum. We found significantly reduced levels of all three proteins in the association cortices and in hippocampus in AD. Our data show that the protein levels are reduced in specific areas, restricted to neuronal populations that are known to degenerate in AD. Due to the similarity of the expression of APP, PS-1 and rab3a, it is tempting to speculate whether there is a functional relationship between these proteins. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:243 / 250
页数:8
相关论文
共 78 条
[1]   PREVALENCE OF DEMENTIA DISORDERS IN INSTITUTIONALIZED SWEDISH OLD-PEOPLE - THE WORK LOAD IMPOSED BY CARING FOR THESE PATIENTS [J].
ADOLFSSON, R ;
GOTTFRIES, CG ;
NYSTROM, L ;
WINBLAD, B .
ACTA PSYCHIATRICA SCANDINAVICA, 1981, 63 (03) :225-244
[2]   HISTOPATHOLOGICAL CRITERIA FOR PROGRESSIVE DEMENTIA DISORDERS - CLINICAL-PATHOLOGICAL CORRELATION AND CLASSIFICATION BY MULTIVARIATE DATA-ANALYSIS [J].
ALAFUZOFF, I ;
IQBAL, K ;
FRIDEN, H ;
ADOLFSSON, R ;
WINBLAD, B .
ACTA NEUROPATHOLOGICA, 1987, 74 (03) :209-225
[3]   Profiles of amyloid precursor and presenilin 2-like proteins are correlated during development of the mouse hypothalamus [J].
Apert, C ;
Czech, C ;
Faivre-Bauman, A ;
Loudes, C ;
Pradier, L ;
Epelbaum, J .
JOURNAL OF NEUROENDOCRINOLOGY, 1998, 10 (02) :101-109
[4]   EXPRESSION PATTERNS OF BETA-AMYLOID PRECURSOR PROTEIN (BETA-APP) IN NEURAL AND NONNEURAL HUMAN TISSUES FROM ALZHEIMERS-DISEASE AND CONTROL SUBJECTS [J].
ARAI, H ;
LEE, VMY ;
MESSINGER, ML ;
GREENBERG, BD ;
LOWERY, DE ;
TROJANOWSKI, JQ .
ANNALS OF NEUROLOGY, 1991, 30 (05) :686-693
[5]   EARLY AND RAPID DE-NOVO SYNTHESIS OF ALZHEIMER BETA-A4-AMYLOID PRECURSOR PROTEIN (APP) IN ACTIVATED MICROGLIA [J].
BANATI, RB ;
GEHRMANN, J ;
CZECH, C ;
MONNING, U ;
JONES, LL ;
KONIG, G ;
BEYREUTHER, K ;
KREUTZBERG, GW .
GLIA, 1993, 9 (03) :199-210
[6]   Alteration in brain presenilin 1 mRNA expression in early onset familial Alzheimer's disease [J].
Barton, AJL ;
Crook, BW ;
Karran, EH ;
Brown, F ;
Dewar, D ;
Mann, DMA ;
Pearson, RCA ;
Graham, DI ;
Hardy, J ;
Hutton, M ;
Duff, K ;
Goate, AM ;
Clark, RF ;
Roberts, GW .
NEURODEGENERATION, 1996, 5 (03) :213-218
[7]   Proteolytic fragments of Alzheimer's disease-associated presenilin 1 are present in synaptic organelles and growth cone membranes of rat brain [J].
Beher, D ;
Elle, C ;
Underwood, J ;
Davis, JB ;
Ward, R ;
Karran, E ;
Masters, CL ;
Beyreuther, K ;
Multhaup, G .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (04) :1564-1573
[8]   Developmental regulation of presenilin mRNA expression parallels notch expression [J].
Berezovska, O ;
Xia, MQ ;
Page, K ;
Wasco, W ;
Tanzi, RE ;
Hyman, BT .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1997, 56 (01) :40-44
[9]   Synaptic pathology in Alzheimer's disease: Relation to severity of dementia, but not to senile plaques, neurofibrillary tangles, or the ApoE4 allele [J].
Blennow, K ;
Bogdanovic, N ;
Alafuzoff, I ;
Ekman, R ;
Davidsson, P .
JOURNAL OF NEURAL TRANSMISSION, 1996, 103 (05) :603-618
[10]  
Bogdanovic N, 1995, NEUROPATHOLOGICAL DI, P20