The Triggering Receptor Expressed on Myeloid Cells 2 Binds Apolipoprotein E

被引:268
作者
Bailey, Charles C. [1 ]
DeVaux, Lindsey B. [1 ]
Farzan, Michael [1 ]
机构
[1] Scripps Res Inst, Dept Immunobiol & Microbial Sci, Jupiter, FL 33458 USA
关键词
ALZHEIMERS-DISEASE; FRONTOTEMPORAL DEMENTIA; MICROGLIAL RESPONSE; TYPE-4; ALLELE; TREM2; MUTATIONS; RISK; PHAGOCYTOSIS; RECOGNITION; CLEARANCE;
D O I
10.1074/jbc.M115.677286
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The triggering receptor expressed on myeloid cells 2 (TREM2) is an Ig-like V-type receptor expressed by populations of myeloid cells in the central nervous system and periphery. Loss-of-function mutations in TREM2 cause a progressive, fatal neurodegenerative disorder called Nasu-Hakola disease. In addition, a TREM2 R47H coding variant was recently identified as a risk factor for late-onset Alzheimer disease. TREM2 binds various polyanionic molecules but no specific protein ligands have been identified. Here we show that TREM2 specifically binds apolipoprotein E, a well established participant in Alzheimer disease. TREM2-Ig fusions efficiently precipitate ApoE from cerebrospinal fluid and serum. TREM2 also binds recombinant ApoE in solution and immobilized ApoE as detected by ELISA. Furthermore, the Alzheimer disease-associated R47H mutation, and other artificial mutations introduced in the same location, markedly reduced the affinity of TREM2 for ApoE. These findings reveal a link between two Alzheimer disease risk factors and may provide important clues to the pathogenesis of Nasu-Hakola disease and other neurodegenerative disorders.
引用
收藏
页码:26033 / 26042
页数:10
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