Nakahashi Chigusa, Tahara-Hanaoka Satoko, Totsuka Naoya, Okoshi Yasushi, Takai Toshiyuki, Ohkohchi Nobuhiro, Honda Shin-Ichiro, Shibuya Kazuko, Shibuya Akira
Department of Immunology, Institute of Basic Medical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Ibaraki, Japan.
J Immunol. 2007 Jan 15;178(2):765-70. doi: 10.4049/jimmunol.178.2.765.
Certain activating immune receptors expressed on myeloid cells noncovalently associate with either DAP12 or FcepsilonRIgamma (FcRgamma chain), the ITAM-bearing transmembrane adapter proteins. An activating receptor, myeloid-associated Ig-like receptor (MAIR) II, is expressed on a subset of B cells and macrophages in the spleen and peritoneal cavity of mice and associates with DAP12 in these cells. However, we demonstrate here that cross-linking MAIR-II with mAb induced secretion of a significant amount of the inflammatory cytokines TNF-alpha and IL-6 from DAP12(-/-) as well as wild-type (WT) peritoneal macrophages. We show that MAIR-II associates with not only DAP12 but also FcRgamma chain homodimers in peritoneal macrophages. LPS enhanced the FcRgamma chain expression and FcRgamma chain-dependent cell surface expression of MAIR-II and had additive effects on MAIR-II-mediated inflammatory cytokine secretion from peritoneal macrophages. The lysine residue in the transmembrane region of MAIR-II was involved in the association with FcRgamma chain as well as DAP12. Our findings present the first case of an activating receptor that uses either DAP12 or FcRgamma chain as a signaling adapter. The FcRgamma chain may provide cooperation with and/or compensation for DAP12 in MAIR-II-mediated inflammatory responses by peritoneal macrophages.
髓系细胞上表达的某些激活型免疫受体与含免疫受体酪氨酸活化基序(ITAM)的跨膜衔接蛋白DAP12或FcεRIγ(FcRγ链)非共价结合。一种激活型受体,即髓系相关免疫球蛋白样受体(MAIR)II,在小鼠脾脏和腹腔的一部分B细胞和巨噬细胞上表达,并在这些细胞中与DAP12结合。然而,我们在此证明,用单克隆抗体使MAIR-II交联可诱导DAP12基因敲除小鼠(DAP12(-/-))以及野生型(WT)腹腔巨噬细胞分泌大量炎性细胞因子TNF-α和IL-6。我们发现,MAIR-II在腹腔巨噬细胞中不仅与DAP12结合,还与FcRγ链同二聚体结合。脂多糖(LPS)增强了FcRγ链的表达以及MAIR-II依赖FcRγ链的细胞表面表达,并对MAIR-II介导的腹腔巨噬细胞炎性细胞因子分泌有累加效应。MAIR-II跨膜区的赖氨酸残基参与了与FcRγ链以及DAP12的结合。我们的研究结果首次揭示了一种激活型受体可利用DAP12或FcRγ链作为信号转导衔接蛋白的情况。在MAIR-II介导的腹腔巨噬细胞炎性反应中,FcRγ链可能与DAP12协同作用和/或对其起到补偿作用。