小胶质细胞
载脂蛋白E
优势比
等位基因
阿尔茨海默病
多发性硬化
特雷姆2
疾病
中枢神经系统
生物
免疫学
医学
内科学
基因
遗传学
内分泌学
炎症
作者
Patrick C. G. Haddick,Jessica L. Larson,Nisha Rathore,Tushar Bhangale,Qui Phung,Karpagam Srinivasan,David V. Hansen,Jennie R. Lill,Margaret A. Pericak‐Vance,Jonathan L. Haines,Lindsay A. Farrer,John Kauwe,Gerard D. Schellenberg,Carlos Cruchaga,Alison Goate,Timothy W. Behrens,Ryan J. Watts,Robert Graham,Joshua S. Kaminker,Marcel van der Brug
摘要
The common p.D358A variant (rs2228145) in IL-6R is associated with risk for multiple diseases and with increased levels of soluble IL-6R in the periphery and central nervous system (CNS). Here, we show that the p.D358A allele leads to increased proteolysis of membrane bound IL-6R and demonstrate th at IL-6R peptides with A358 are more susceptible to cleavage by ADAM10 and ADAM17. IL-6 responsive genes were identified in primary astrocytes and microglia and an IL-6 gene signature was increased in the CNS of late onset Alzheimer's disease subjects in an IL6R allele dependent manner. We conducted a screen to identify variants associated with the age of onset of Alzheimer's disease in APOE ɛ4 carriers. Across five datasets, p.D358A had a meta P = 3 ×10-4 and an odds ratio = 1.3, 95% confidence interval 1.12 –1.48. Our study suggests that a common coding region variant of the IL-6 receptor results in neuroinflammatory changes that may influence the age of onset of Alzheimer's disease in APOE ɛ4 carriers.
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