NEUROPATHOLOGY AND APOLIPOPROTEIN-E PROFILE OF AGED CHIMPANZEES - IMPLICATIONS FOR ALZHEIMER-DISEASE

被引:144
作者
GEARING, M
REBECK, GW
HYMAN, BT
TIGGES, J
MIRRA, SS
机构
[1] VET AFFAIRS MED CTR,DEPT LAB MED & PATHOL,ATLANTA,GA 30322
[2] EMORY UNIV,SCH MED,ATLANTA,GA 30322
[3] MASSACHUSETTS GEN HOSP,DEPT NEUROL,BOSTON,MA 02114
[4] HARVARD UNIV,BOSTON,MA 02114
[5] EMORY UNIV,YERKES REG PRIMATE RES CTR,ATLANTA,GA 30322
关键词
AMYLOID; PRIMATE; RHESUS MONKEY; AGING;
D O I
10.1073/pnas.91.20.9382
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neuropathological findings in three aged chimpanzees were compared with those in rhesus monkeys and individuals with Alzheimer disease. Senile plaques and blood vessels were immunoreactive for amyloid beta-protein and apolipoprotein E (apoE) in the nonhuman primates, recapitulating findings in human aging and Alzheimer disease. Neurofibrillary tangles, another hallmark of Alzheimer disease, were absent. PCR/restriction-enzyme analysis in chimpanzees revealed an APOE profile similar to the human APOE type 4 allele associated with an increased risk of Alzheimer disease. These findings militate against the hypothesis that the absence of APOE type 3 allele predisposes to neurofibrillary tangle formation and support the value of aged primates for exploring mechanisms of amyloid processing and the role of apoE.
引用
收藏
页码:9382 / 9386
页数:5
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