Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, No.5 Donghai Middle Road, Qingdao, Shandong Province 266071, China.
Mol Neurobiol. 2012 Apr;45(2):314-26. doi: 10.1007/s12035-012-8237-1. Epub 2012 Jan 25.
Genetic variation in clusterin gene, also known as apolipoprotein J, has been associated with Alzheimer's disease (AD) through replicated genome-wide studies, and plasma clusterin levels are associated with brain atrophy, baseline prevalence and severity, and rapid clinical progression in patients with AD, highlighting the importance of clusterin in AD pathogenesis. Emerging data suggest that clusterin contributes to AD through various pathways, including amyloid-β aggregation and clearance, lipid metabolism, neuroinflammation, and neuronal cell cycle control and apoptosis. Moreover, epigenetic regulation of the clusterin expression also seems to play an important role in the pathogenesis of AD. Emerging knowledge of the contribution of clusterin to the pathogenesis of AD presents new opportunities for AD therapy.
载脂蛋白 J 基因(也称为簇集素)的遗传变异与通过复制的全基因组研究相关阿尔茨海默病(AD),并且血浆簇集素水平与脑萎缩、基线患病率和严重程度以及 AD 患者的快速临床进展相关,突出了簇集素在 AD 发病机制中的重要性。新出现的数据表明,簇集素通过多种途径促进 AD 的发展,包括淀粉样蛋白-β聚集和清除、脂代谢、神经炎症以及神经元细胞周期控制和凋亡。此外,簇集素表达的表观遗传调节似乎在 AD 的发病机制中也起着重要作用。簇集素对 AD 发病机制的贡献的新知识为 AD 治疗提供了新的机会。