High density lipoprotein decreases beta-amyloid toxicity in cortical cell culture

被引:25
作者
Farhangrazi, ZS
Ying, H
Bu, GJ
Dugan, LL
Fagan, AM
Choi, DW
Holtzman, DM
机构
[1] WASHINGTON UNIV,SCH MED,DEPT NEUROL,ST LOUIS,MO 63110
[2] WASHINGTON UNIV,SCH MED,CTR STUDY NERVOUS SYST INJURY,ST LOUIS,MO 63110
[3] WASHINGTON UNIV,SCH MED,EDWARD MALLINCKRODT DEPT PEDIAT,ST LOUIS,MO 63110
[4] WASHINGTON UNIV,SCH MED,DEPT MOL BIOL & PHARMACOL,ST LOUIS,MO 63110
关键词
Alzheimer's disease; apolipoprotein E; beta-amyloid; high density lipoprotein;
D O I
10.1097/00001756-199703240-00013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A hallmark of Alzheimer's disease (AD) is the extracellular deposition and accumulation of a 39-43 amino peptide, known as the amyloid beta (A beta) protein, within the brain. It has been postulated that A beta may in some way contribute directly to AD pathogenesis. The epsilon 4 allele of apolipoprotein E (apoE) is a major AD risk factor. Since both apoE and A are components of lipoproteins in plasma and cerebrospinal fluid, we asked whether lipoproteins and apoE isoforms would modify the toxicity of A beta(1-42) in cortical cell cultures. We show that high density lipoprotein with or without apoE reduces A beta toxicity and that apoE in the absence of lipoproteins does not affect A beta toxicity. These results suggest that interactions between A beta and lipoproteins in the brain could influence AD pathogenesis.
引用
收藏
页码:1127 / 1130
页数:4
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