Cancer and Inflammation Program, Laboratory of Experimental Immunology, SAIC-Frederick, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD, 21702, USA.
Immunogenetics. 2014 Jan;66(1):1-8. doi: 10.1007/s00251-013-0730-9. Epub 2013 Oct 6.
Leukocyte immunoglobulin-like receptor (LILR)B3 and LILRA6 represent a pair of inhibitory/activating receptors with identical extracellular domains and unknown ligands. LILRB3 can mediate inhibitory signaling via immunoreceptor tyrosine-based inhibition motifs in its cytoplasmic tail whereas LILRA6 can signal through association with an activating adaptor molecule, FcRγ, which bears a cytoplasmic tail with an immunoreceptor tyrosine-based activation motif. The receptors are encoded by two highly polymorphic neighboring genes within the leukocyte receptor complex on human chromosome 19. Here, we report that the two genes display similar levels of single nucleotide polymorphisms with the majority of polymorphic sites being identical. In addition, the LILRA6 gene exhibits copy number variation (CNV) whereas LILRB3 does not. A screen of healthy Caucasians indicated that 32 % of the subjects possessed more than two copies of LILRA6, whereas 4 % have only one copy of the gene per diploid genome. Analysis of mRNA expression in the major fractions of PBMCs showed that LILRA6 is primarily expressed in monocytes, similarly to LILRB3, and its expression level correlates with copy number of the gene. We suggest that the LILRA6 CNV may influence the level of the activating receptor on the cell surface, potentially affecting signaling upon LILRB3/A6 ligation.
白细胞免疫球蛋白样受体 (LILR)B3 和 LILRA6 代表一对具有相同细胞外结构域和未知配体的抑制/激活受体。LILRB3 可以通过其细胞质尾部中的免疫受体酪氨酸抑制基序介导抑制信号,而 LILRA6 可以通过与具有细胞质尾部的激活衔接分子 FcRγ 结合来信号传递,该分子具有免疫受体酪氨酸激活基序。这些受体由人类 19 号染色体上白细胞受体复合物内的两个高度多态性相邻基因编码。在这里,我们报告这两个基因显示出相似水平的单核苷酸多态性,大多数多态性位点是相同的。此外,LILRA6 基因表现出拷贝数变异 (CNV),而 LILRB3 则没有。对健康白种人的筛查表明,32%的受试者具有超过两个 LILRA6 拷贝,而 4%的受试者每个二倍体基因组只有一个 LILRA6 基因拷贝。对主要 PBMC 分数中的 mRNA 表达进行分析表明,LILRA6 主要在单核细胞中表达,与 LILRB3 相似,其表达水平与基因的拷贝数相关。我们认为 LILRA6 的 CNV 可能会影响细胞表面上激活受体的水平,从而可能影响 LILRB3/A6 结合后的信号传递。