Carr William H, Rosen David B, Arase Hisashi, Nixon Douglas F, Michaelsson Jakob, Lanier Lewis L
Department of Microbiology and Immunology, Cancer Research Institute and Biomedical Sciences Graduate Program, University of California-San Francisco, CA 94143, USA.
J Immunol. 2007 Jan 15;178(2):647-51. doi: 10.4049/jimmunol.178.2.647.
The killer cell Ig-like receptor (KIR) gene, KIR3DS1, has been implicated in slowing disease progression in HIV infection; however, little is known about its expression, function, or ligand specificity. Using retrovirally transduced NKL cells and peripheral blood NK cells from KIR3DS1-positive donors we assessed expression of this gene by flow cytometry and its function by in vitro assays measuring KIR3DS1-induced cell-mediated cytotoxicity and cytokine production. In the present study, we demonstrate that KIR3DS1 is expressed on peripheral blood NK cells and triggers both cytotoxicity and IFN-gamma production. Using cotransfection and coimmunoprecipitation, we found that KIR3DS1 associates with the ITAM-bearing adaptor, DAP12. Soluble KIR3DS1-Ig fusion proteins did not bind to EBV-transformed B lymphoid cell lines transfected with HLA-Bw4 80I or 80T allotypes, suggesting that if KIR3DS1 does recognize HLA-Bw4 ligands, this may be peptide dependent.
杀伤细胞免疫球蛋白样受体(KIR)基因KIR3DS1被认为与减缓HIV感染的疾病进展有关;然而,对其表达、功能或配体特异性却知之甚少。我们利用逆转录病毒转导的NKL细胞以及来自KIR3DS1阳性供体的外周血NK细胞,通过流式细胞术评估该基因的表达,并通过体外测定KIR3DS1诱导的细胞介导的细胞毒性和细胞因子产生来评估其功能。在本研究中,我们证明KIR3DS1在外周血NK细胞上表达,并触发细胞毒性和IFN-γ产生。通过共转染和共免疫沉淀,我们发现KIR3DS1与携带免疫受体酪氨酸激活基序(ITAM)的接头蛋白DAP12相关联。可溶性KIR3DS1-Ig融合蛋白不与转染了HLA-Bw4 80I或80T同种异型的EBV转化的B淋巴母细胞系结合,这表明如果KIR3DS1确实识别HLA-Bw4配体,这可能是肽依赖性的。