Immune reactive cells in senile plaques and cognitive decline in Alzheimer's disease

被引:181
作者
Vehmas, AK
Kawas, CH
Stewart, WF
Troncoso, JC
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Div Neuropathol, Baltimore, MD 21205 USA
[2] Univ Calif Irvine, Dept Neurol, Irvine, CA 92697 USA
[3] Johns Hopkins Univ, Sch Hyg & Publ Hlth, Dept Epidemiol, Baltimore, MD USA
关键词
astrocyte; A beta-peptide; dementia; immunity; microglia; Tau-protein;
D O I
10.1016/S0197-4580(02)00090-8
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
We examined the associations of postmortem neocortical immunoreactivities for microglia, astrocytes, Abeta and Tau with cognitive changes in clinically characterized subjects with pathological diagnoses (CERAD classification) of definite AD (9), possible AD (15) and age-matched controls (11). By measuring the fractional area (FA) of immunoreactivity, we found that Abeta deposits appear early in the pathogenesis of Abeta, but cannot account for cognitive decline. We found a significant increases in FA for microglia in possible AD cases (nondemented) compared to controls (P < 0.05) and in FA for astrocytes in definite AD (demented) compared to possible AD (P < 0.01). Tau immunoreactivity was observed only in the neuropil of definite AD cases (P < 0.001). The significant increase in microglia between controls and AD possible cases suggests that activation of microglia occurs in the early pathogenesis of AD, whereas the significant association between astrocytic reaction and dementia, suggests that these cells play a role in the late stage of the disease, when dementia develops. Tau immunoreactivity appears as the strongest morphological correlate of dementia. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:321 / 331
页数:11
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