Permanne B, Perez C, Soto C, Frangione B, Wisniewski T
Department of Pathology, New York University Medical Center, New York 10016, USA.
Biochem Biophys Res Commun. 1997 Nov 26;240(3):715-20. doi: 10.1006/bbrc.1997.7727.
The inheritance of the apolipoprotein (apo) E4 allele is an important risk factor for late-onset Alzheimer's disease (AD). A major component of the Alzheimer's disease neuritic plaques is amyloid beta (A beta). We previously identified apoE/A beta complexes within neuritic plaques (1). It was not known if this interaction takes place before or after A beta peptides become incorporated into neuritic plaques. To address this question we sought evidence of apoE complexes with brain soluble A beta peptides in AD and control patients. In addition, numerous proteins have been shown to bind A beta peptides in vitro. It is not know if any of these bind brain sA beta in vivo. We found evidence for the presence of apoE/dimeric sA beta complexes in the AD brain and could not detect complexes with other A beta peptide binding proteins. The binding of sA beta to apoE may be one factor influencing its clearance from the brain and/or its conformational state.
载脂蛋白(apo)E4等位基因的遗传是晚发性阿尔茨海默病(AD)的一个重要风险因素。阿尔茨海默病神经炎性斑块的一个主要成分是β淀粉样蛋白(Aβ)。我们之前在神经炎性斑块中鉴定出了apoE/Aβ复合物(1)。尚不清楚这种相互作用是在Aβ肽整合到神经炎性斑块之前还是之后发生。为了解决这个问题,我们在AD患者和对照患者中寻找apoE与脑可溶性Aβ肽形成复合物的证据。此外,已有大量蛋白质在体外被证明可与Aβ肽结合。尚不清楚这些蛋白质中是否有任何一种在体内与脑可溶性Aβ(sAβ)结合。我们发现AD脑内存在apoE/二聚体sAβ复合物的证据,且未检测到与其他Aβ肽结合蛋白形成的复合物。sAβ与apoE的结合可能是影响其从脑内清除和/或其构象状态的一个因素。