载脂蛋白E
基因亚型
淀粉样蛋白(真菌学)
新陈代谢
载脂蛋白B
脑脊液
机制(生物学)
体内
阿尔茨海默病
化学
生物
疾病
内分泌学
内科学
细胞生物学
神经科学
生物化学
医学
病理
胆固醇
遗传学
基因
哲学
认识论
作者
Philip B. Verghese,Joseph M. Castellano,Kanchan Garai,Yinong Wang,Hong Jiang,Aarti R. Shah,Guojun Bu,Carl Frieden,David M. Holtzman
标识
DOI:10.1073/pnas.1220484110
摘要
Significance It has been proposed that differential physical interactions of apolipoprotein E (apoE) isoforms with soluble amyloid-β (Aβ) in brain fluids influence the metabolism of Aβ, providing a major mechanism to account for how APOE influences Alzheimer’s disease risk. The current study challenges this proposal and clearly shows that lipoproteins containing apoE isoforms are unlikely to play a significant role in Aβ metabolism by binding directly to Aβ in physiological fluids such as cerebrospinal fluid or interstitial fluid. Our in vitro and in vivo results suggest that apoE isoforms influence Aβ metabolism by competing for the same clearance pathways within the brain.
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