beta-amyloid (A beta) deposition in the brains of aged orangutans

被引:95
作者
Gearing, M
Tigges, J
Mori, H
Mirra, SS
机构
[1] VET AFFAIRS MED CTR,DECATUR,GA 30033
[2] EMORY UNIV,SCH MED,DEPT PATHOL & LAB MED,DECATUR,GA 30033
[3] EMORY UNIV,YERKES REG PRIMATE RES CTR,SCH MED,ATLANTA,GA 30322
[4] EMORY UNIV,DEPT ANAT & CELL BIOL,SCH MED,ATLANTA,GA 30322
[5] TOKYO INST PSYCHIAT,DEPT MOL BIOL,TOKYO,JAPAN
关键词
amyloid; apolipoprotein E; orangutan; great ape; nonhuman primate; Alzheimer's disease; aging; senile plaque;
D O I
10.1016/S0197-4580(97)00012-2
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
While aged monkeys of several species show cerebral amyloid deposition in senile plaques and blood vessels similar to that seen in human aging and Alzheimer's disease (AD), studies of great apes have been limited. Using histological and immunohistochemical methods, we examined the brains of four orangutans aged IO, 28, 31, and 36 years. We encountered sparse beta-amyloid (A beta)-immunoreactive, silver-negative plaque-like structures in the brains of the three older apes. The 36-year-old orangutan also evidenced small A beta-positive deposits in subcortical white matter and sparse vascular amyloid deposition, primarily in meningeal vessels. Neurofibrillary tangles were not detected on silver stains or on tau or ubiquitin immunohistochemistry. Many of the A beta-positive plaque-like deposits in the orangutans were apolipoprotein E-immunoreactive, as we have previously reported in aged rhesus monkeys and an aged chimpanzee. Also, paralleling our earlier findings in these nonhuman primates, A beta(40) in plaques was more prominent in the orangutan than is typically seen in human aging, AD, and Down syndrome. These intriguing species differences may provide clues to the mechanisms of amyloid deposition and the development of neuropathologic changes in AD. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:139 / 146
页数:8
相关论文
共 35 条
[1]  
BOWDEN DM, 1984, ADV VET SCI COMP MED, V28, P305
[2]  
Cork L., 1993, NONHUMAN PRIMATES, V2, P173
[3]  
Cummings BJ, 1996, NEUROBIOL AGING, V17, P653
[4]  
Fukumoto H, 1996, AM J PATHOL, V148, P259
[5]   NEUROPATHOLOGY AND APOLIPOPROTEIN-E PROFILE OF AGED CHIMPANZEES - IMPLICATIONS FOR ALZHEIMER-DISEASE [J].
GEARING, M ;
REBECK, GW ;
HYMAN, BT ;
TIGGES, J ;
MIRRA, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) :9382-9386
[6]   A beta-peptide length and apolipoprotein E genotype in Alzheimer's disease [J].
Gearing, M ;
Mori, H ;
Mirra, SS .
ANNALS OF NEUROLOGY, 1996, 39 (03) :395-399
[7]   A beta(40) is a major form of beta-amyloid in nonhuman primates [J].
Gearing, M ;
Tigges, J ;
Mori, H ;
Mirra, SS .
NEUROBIOLOGY OF AGING, 1996, 17 (06) :903-908
[8]   APOLIPOPROTEIN-E EPSILON-4 AND CEREBRAL-HEMORRHAGE ASSOCIATED WITH AMYLOID ANGIOPATHY [J].
GREENBERG, SM ;
REBECK, GW ;
VONSATTEL, JPG ;
GOMEZISLA, T ;
HYMAN, BT .
ANNALS OF NEUROLOGY, 1995, 38 (02) :254-259
[9]  
GUILLOUD MB, 1969, RECENT ADV PRIMATOL, V3, P143
[10]   VISUALIZATION OF A-BETA-42(43) AND A-BETA-40 IN SENILE PLAQUES WITH END-SPECIFIC A-BETA MONOCLONALS - EVIDENCE THAT AN INITIALLY DEPOSITED SPECIES IS A-BETA-42(43) [J].
IWATSUBO, T ;
ODAKA, A ;
SUZUKI, N ;
MIZUSAWA, H ;
NUKINA, N ;
IHARA, Y .
NEURON, 1994, 13 (01) :45-53