Westgaard Ingunn H, Berg Siri F, Vaage John T, Wang Lawrence L, Yokoyama Wayne M, Dissen Erik, Fossum Sigbjørn
Department of Anatomy, Institute of Basic Medical Sciences, University of Oslo, Box 1105 Blindern, N-0317 Oslo, Norway.
J Leukoc Biol. 2004 Dec;76(6):1200-6. doi: 10.1189/jlb.0903428. Epub 2004 Sep 8.
NKp46 has been identified in the human, rat, mouse, monkey, and cattle. We have generated a monoclonal antibody, WEN23, against rat NKp46. By flow cytometry, NKp46 is expressed by all natural killer (NK) cells but not by T cells, B cells, granulocytes, monocytes, dendritic cells, or macrophages. Thus, NKp46/WEN23 is the first NK cell-specific marker in the rat. In a redirected lysis assay, preincubation of the effector cells with WEN23 augmented lysis of the Fc receptor (FcR)+ murine tumor target cells, indicating that NKp46 is an activating NK cell receptor. Moreover, preincubation of the effector cells with WEN23 F(ab')2 fragments reduced killing of target cells, confirming the activating function of NKp46 and indicating that the mouse tumor target cells express a ligand for rat NKp46. Lysis of FcR- mouse and human tumor target cells was reduced after incubation of effector cells with WEN23, suggesting that rat NKp46 recognizes a ligand that is conserved between primates and rodents. By Western blot and immunoprecipitation using WEN23, NKp46 is expressed as a monomer of approximately 47 kDa in interleukin-2-activated NK cells. The immunoreceptor tyrosine-based activation motif bearing adaptor proteins CD3zeta and the gamma chain of FcRI for IgE (FcepsilonRIgamma) with NKp46 from lysates of NK cells, indicating that rat NKp46 activates NK cell cytotoxicity by similar pathways as CD16.
NKp46已在人类、大鼠、小鼠、猴子和牛中被鉴定出来。我们制备了一种针对大鼠NKp46的单克隆抗体WEN23。通过流式细胞术检测,NKp46在所有自然杀伤(NK)细胞中表达,而在T细胞、B细胞、粒细胞、单核细胞、树突状细胞或巨噬细胞中不表达。因此,NKp46/WEN23是大鼠中首个NK细胞特异性标志物。在重定向裂解试验中,效应细胞与WEN23预孵育可增强对Fc受体(FcR)+小鼠肿瘤靶细胞的裂解,表明NKp46是一种激活型NK细胞受体。此外,效应细胞与WEN23 F(ab')2片段预孵育可降低对靶细胞的杀伤,证实了NKp46的激活功能,并表明小鼠肿瘤靶细胞表达大鼠NKp46的配体。效应细胞与WEN23孵育后,FcR - 小鼠和人类肿瘤靶细胞的裂解减少,这表明大鼠NKp46识别一种在灵长类动物和啮齿动物之间保守的配体。通过使用WEN23进行蛋白质免疫印迹和免疫沉淀分析,在白细胞介素 - 2激活的NK细胞中,NKp46以约47 kDa的单体形式表达。基于免疫受体酪氨酸的激活基序的衔接蛋白CD3ζ和IgE的FcRI的γ链(FcepsilonRIgamma)与NK细胞裂解物中的NKp46结合,表明大鼠NKp46通过与CD16相似的途径激活NK细胞的细胞毒性。
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