Human macrophage C-type lectin forms a heteromeric receptor complex with Mincle but not Dectin-2

被引:5
|
作者
Blankson, Vera [1 ]
Lobato-Pascual, Ana [1 ]
Saether, Per Christian [1 ]
Fossum, Sigbjorn [1 ]
Dissen, Erik [1 ]
Daws, Michael R. [1 ]
机构
[1] Univ Oslo, Inst Basic Med Sci, Div Anat, Oslo, Norway
关键词
cell activation; cell surface molecules; cells; dendritic cells; molecules; monocytes; macrophages; neutrophils; processes; PATTERN-RECOGNITION RECEPTOR; ACTIVATING RECEPTOR; MYELOID CELLS; MCL; CLECSF8; CLEC4D;
D O I
10.1111/sji.13149
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MCL, Mincle and Dectin-2 are C-type lectin receptors expressed by subsets of myeloid cells, and their genes cluster together in the APLEC/Dectin-2 gene complex. We have previously shown that MCL and Mincle form a heterodimer in the rat, and others have shown that MCL and Dectin-2 form a heterodimer in the mouse. In the rat, Dectin-2 is a pseudogene, but here, we examine the association of the three receptors in human. In co-transfection experiments analyzed with flow cytometry and immunoprecipitation, we here show that human MCL and Mincle form a disulphide-linked heterodimer that associates with the signalling adaptor molecule Fc epsilon RI gamma, in accordance with our previous findings in the rat. In contrast to previous findings in the rat, data in this paper indicate a direct association of MCL with Fc epsilon RI gamma, as previously shown for mouse MCL. We were unable to demonstrate the formation of a heterodimer between human MCL and Dectin-2. Thus, despite similarities, there may be important differences in the conformation of these receptors between rat, mouse and human, and this may have functional consequences.
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页数:7
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