Beta-amyloid expression, release and extracellular deposition in aged rat brain slices

被引:51
作者
Marksteiner, J. [1 ]
Humpel, C. [1 ]
机构
[1] Innsbruck Med Univ, Dept Gen Psychiat, Lab Psychiat & Exp Alzheimers Res, Innsbruck, Austria
基金
奥地利科学基金会;
关键词
Alzheimer; beta-amyloid; brain slice; ApoE4;
D O I
10.1038/sj.mp.4002072
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is characterized by beta-amyloid plaques, tau pathology, cholinergic cell death and inflammation. The aim of this study was to investigate whether beta-amyloid is generated, released and extracellularly deposited in organotypic brain slices. In developing slices, no amyloid-precursor protein (APP) was detectable; however, there was a strong upregulation in aging slices. In such slices, rat beta-amyloid(1 - 42) and -(1 - 40) peptides were found using four sequence-specific antibodies. APP and beta-amyloid were expressed in neurons and to a lesser extent in astrocytes. Beta-amyloid was secreted into the medium. Beta-amyloid was located extracellularly when aging slices were incubated with medium at pH 6.0 including apolipoprotein E4 (ApoE4). It is concluded that aging organotypic brain slices express beta-amyloid and that acidosis induces cell death with efflux of b-amyloid and extracellular depositions, which is triggered by ApoE4. This novel in vitro model may enable us to investigate further the pathological cascade for AD and may be useful to explore future therapeutics.
引用
收藏
页码:939 / 952
页数:14
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