Apolipoprotein E isoform-specific reduction of extracellular amyloid in neuronal cultures

被引:61
作者
Beffert, U
Aumont, N
Dea, D
Lussier-Cacan, S
Davignon, J
Poirier, J
机构
[1] McGill Univ, Douglas Hosp, Res Ctr, Dept Neurol & Neurosurg, Verdun, PQ H4H 1R3, Canada
[2] Clin Res Inst Montreal, Montreal, PQ H2W 1R7, Canada
来源
MOLECULAR BRAIN RESEARCH | 1999年 / 68卷 / 1-2期
关键词
apolipoprotein E; beta-amyloid; Alzheimer's disease;
D O I
10.1016/S0169-328X(99)00073-X
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Both apolipoprotein E (apoE) and amyloid peptides are associated with Alzheimer's disease (AD). Using primary hippocampal neurons, we demonstrate that apoE is capable of reducing potentially toxic extracellular amyloid peptides, likely through a receptor mediated mechanism. We hypothesize that isoform-specific differences in apoE-mediated amyloid clearance and intracellular accumulation may be responsible, at least in part, for the increased number of amyloid plaques observed in apoE epsilon 4 allele AD individuals. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:181 / 185
页数:5
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