Expression and regulation of the orphan receptor RDC1 and its putative ligand in human dendritic and B cells

被引:114
作者
Infantino, S
Moepps, B
Thelen, M
机构
[1] Inst Res Biomed, CH-6500 Bellinzona, Switzerland
[2] Univ Ulm, Dept Pharmacol & Toxicol, Ulm, Germany
关键词
D O I
10.4049/jimmunol.176.4.2197
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Based on phylogenetic analysis and chromosomal mapping, the orphan receptor RDC1 was proposed to be a chemokine receptor. 14 In this study we examined the expression of RDC1 on leukocytes by measuring mRNA levels and receptor expression using a new specific mAb. Both mRNA and protein levels were high in monocytes and B cells, relatively low on immature dendritic cells (DC), and up-regulated during final stages of maturation. Strikingly, in mature plasmacytoid DC the mRNA was up-regulated, but did not correlate with protein surface expression. We indeed report that CpG-activated plasmacytoid DC produce a putative ligand for RDC1, which selectively down-regulates RDC1, but not CXCR4 on primary human B cells. RDC1 expression was found to be tightly regulated during B cell development and differentiation. In blood-derived switch memory B cells, the expression of RDC1 appeared to correlate with the ability to differentiate into plasma cells upon activation, suggesting that RDC1 is a marker for memory B cells, which are competent to become Ab-secreting cells.
引用
收藏
页码:2197 / 2207
页数:11
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