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牛程序性死亡配体2的鉴定与特征分析

Identification and characterization of bovine programmed death-ligand 2.

作者信息

Nishimori Asami, Konnai Satoru, Ikebuchi Ryoyo, Okagawa Tomohiro, Nakajima Chie, Suzuki Yasuhiko, Mingala Claro N, Murata Shiro, Ohashi Kazuhiko

机构信息

Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818.

出版信息

Microbiol Immunol. 2014 Jul;58(7):388-97. doi: 10.1111/1348-0421.12160.

Abstract

Previous reports from this group have indicated that the immunoinhibitory programmed death (PD)-1 receptor and its ligand, PD-L1, are involved in the mechanism of immune evasion of bovine chronic infection. However, no functional analysis of bovine PD-L2 in cattle has been reported. Thus, in this study, the molecular function of bovine PD-L2 was analyzed in vitro. Recombinant PD-L2 (PD-L2-Ig), which comprises an extracellular domain of bovine PD-L2 fused to the Fc portion of rabbit IgG1, was prepared based on the cloned cDNA sequence for bovine PD-L2. Bovine PD-L2-Ig bound to bovine PD-1-expressing cells and addition of soluble bovine PD-1-Ig clearly inhibited the binding of PD-L2-Ig to membrane PD-1 in a dose-dependent manner. Cell proliferation and IFN-γ production were significantly enhanced in the presence of PD-L2-Ig in peripheral blood mononuclear cells (PBMCs) from cattle. Moreover, PD-L2-Ig significantly enhanced IFN-γ production from virus envelope peptides-stimulated PBMCs derived from bovine leukemia virus-infected cattle. Interestingly, PD-L2-Ig-induced IFN-γ production was further enhanced by treatment with anti-bovine PD-1 antibody. These data suggest potential applications of bovine PD-L2-Ig as a therapy for bovine diseases.

摘要

该研究小组之前的报告表明,免疫抑制性程序性死亡(PD)-1受体及其配体PD-L1参与了牛慢性感染的免疫逃逸机制。然而,尚未有关于牛PD-L2在牛体内功能分析的报道。因此,在本研究中,对牛PD-L2的分子功能进行了体外分析。基于克隆的牛PD-L2 cDNA序列,制备了重组PD-L2(PD-L2-Ig),其包含与兔IgG1的Fc部分融合的牛PD-L2胞外域。牛PD-L2-Ig与表达牛PD-1的细胞结合,添加可溶性牛PD-1-Ig可明显剂量依赖性地抑制PD-L2-Ig与膜PD-1的结合。在牛外周血单核细胞(PBMCs)中存在PD-L2-Ig时,细胞增殖和IFN-γ产生显著增强。此外,PD-L2-Ig显著增强了来自牛白血病病毒感染牛的病毒包膜肽刺激的PBMCs的IFN-γ产生。有趣的是,用抗牛PD-1抗体处理可进一步增强PD-L2-Ig诱导的IFN-γ产生。这些数据表明牛PD-L2-Ig作为牛疾病治疗方法的潜在应用。

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