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CD33 阿尔茨海默病基因座:改变单核细胞功能和淀粉样蛋白生物学。

CD33 Alzheimer's disease locus: altered monocyte function and amyloid biology.

机构信息

Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Nat Neurosci. 2013 Jul;16(7):848-50. doi: 10.1038/nn.3435. Epub 2013 May 23.

Abstract

In our functional dissection of the CD33 Alzheimer's disease susceptibility locus, we found that the rs3865444(C) risk allele was associated with greater cell surface expression of CD33 in the monocytes (t50 = 10.06, P(joint) = 1.3 × 10(-13)) of young and older individuals. It was also associated with diminished internalization of amyloid-β 42 peptide, accumulation of neuritic amyloid pathology and fibrillar amyloid on in vivo imaging, and increased numbers of activated human microglia.

摘要

在我们对 CD33 阿尔茨海默病易感性位点的功能解剖中,我们发现 rs3865444(C) 风险等位基因与年轻人和老年人单核细胞中 CD33 的细胞表面表达增加有关(t50 = 10.06,P(joint) = 1.3×10(-13))。它还与淀粉样蛋白-β 42 肽的内化减少、神经突淀粉样病理学和体内成像上纤维状淀粉样物质的积累以及激活的人小胶质细胞数量的增加有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e640/3703870/adb0531f6939/nihms481627f1.jpg

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