Simakova Olga, Arispe Nelson J
Department of Anatomy, Physiology and Genetics, and Institute for Molecular Medicine, Uniformed Services University School of Medicine (USUHS), Bethesda, MD 20814, USA.
Int J Alzheimers Dis. 2011;2011:917629. doi: 10.4061/2011/917629. Epub 2011 Jun 8.
We performed a fluorescent analysis of the binding of Aβ to the surface membrane of different types of cells lines such as PC12, GT1-7, and ex vivo neurons. Analyses were performed on sorted cells with membrane bound Aβ Competitive binding between Aβ phosphatidyl serine- (PtdSer-) specific binder annexin V and an anti-PtdSer antibody provided compelling data confirming the involvement of PtdSer as one of the surface membrane signal molecules for Aβ. We found that populations of cells that exhibited high surface membrane binding affinity for Aβ also show higher membrane cholesterol levels compared to cells that did not bind Aβ. This direct relationship was upheld in cholesterol-enriched or cholesterol-depleted cell membranes. We conclude that the initial process for the cell-selective binding by Aβ, to later conversion of elemental Aβ units into larger structures such as fibrils or to the potentially toxic ion channel aggregates, is highly influenced by the membrane content of PtdSer and cholesterol in the cell surface membrane.
我们对β-淀粉样蛋白(Aβ)与不同类型细胞系(如PC12、GT1-7)以及离体神经元表面膜的结合进行了荧光分析。对具有膜结合Aβ的分选细胞进行了分析。Aβ与磷脂酰丝氨酸(PtdSer)特异性结合蛋白膜联蛋白V和抗PtdSer抗体之间的竞争性结合提供了有力数据,证实PtdSer作为Aβ的表面膜信号分子之一参与其中。我们发现,与未结合Aβ的细胞相比,对Aβ表现出高表面膜结合亲和力的细胞群体也显示出更高的膜胆固醇水平。这种直接关系在富含胆固醇或胆固醇耗尽的细胞膜中均成立。我们得出结论,Aβ细胞选择性结合的初始过程,以及随后将基本Aβ单元转化为更大结构(如纤维)或潜在有毒离子通道聚集体的过程,受到细胞表面膜中PtdSer和胆固醇膜含量的高度影响。