载脂蛋白E在阿尔茨海默病分子病理机制中的作用

Makoto Michikawa
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摘要

载脂蛋白E (Apo-E)是调节脑内脂质转运和损伤修复的主要胆固醇载体。众所周知,携带epsilon4等位基因的个体比携带更常见的epsilon3等位基因的个体患阿尔茨海默病(AD)的风险更高,而携带epsilon2等位基因的个体患AD的风险更低。ApoE-HDL与几种细胞表面受体结合以传递脂质,也与淀粉样蛋白(Abeta)结合。β被认为是阿尔茨海默病中引发毒性事件,导致突触功能障碍和神经退行性变。已有研究表明,载脂蛋白e异构体在脑内对β聚集和清除有差异调节,并在调节脑脂质转运和线粒体功能方面具有不同的功能。在这篇综述中,我们总结了目前关于Apo-E在中枢神经系统中的知识,特别强调了其产生HDL和清除/降解不同ApoE亚型的HDL结合β的功能。
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[Role of apolipoprotein E in the molecular pathomechanism of Alzheimer disease].

Apolipoprotein E (Apo-E) is a major cholesterol carrier regulating lipid transport and injury repair in the brain. It is known that individuals carrying the epsilon4 allele are at increased risk of Alzheimer disease (AD) compared with those carrying the more common epsilon3 allele, whereas the epsilon2 allele decreases risk. ApoE-HDL binds to several cell-surface receptors to deliver lipids, and also to amyloid-beta (Abeta) proteins. Abeta is thought to initiate toxic events that lead to synaptic dysfunction and neurodegeneration in AD. It has been shown that Apo-E isoforms differentially regulate Abeta aggregation and clearance in the brain, and have distinct functions in regulating brain lipid transport, and mitochondrial function. In this review, we summarize current knowledge about Apo-E in the CNS, with a particular emphasis on its functions to generate HDL and clear/degradate of HDL-bound Abeta with different ApoE isoforms.

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