Wilcox Ryan A, Chapoval Andrei I, Gorski Kevin S, Otsuji Mizuto, Shin Tahiro, Flies Dallas B, Tamada Koji, Mittler Robert S, Tsuchiya Haruo, Pardoll Drew M, Chen Lieping
Department of Immunology, Mayo Clinic, Rochester, MN 55905, USA.
J Immunol. 2002 May 1;168(9):4262-7. doi: 10.4049/jimmunol.168.9.4262.
Interaction between dendritic cells (DCs) and T cells is a prerequisite for the initiation of a T cell response. The molecular nature of this interaction remains to be fully characterized. We report in this work that freshly isolated mouse splenic DCs and bone marrow-derived DCs express CD137 on the cell surface and in soluble form. Triggering CD137 increased the secretion of IL-6 and IL-12 from DCs. More importantly, infusion of an agonistic mAb to CD137 into naive mice enhanced the ability of DCs to stimulate T cell proliferation in response to both alloantigens and a nominal Ag in vitro. This enhancement of DC function is not mediated through activation of T cells, because the effect was also observed in RAG-1 knockout mice that lack T cells. Our findings implicate CD137 as an important receptor involved in the modulation of DC function.
树突状细胞(DCs)与T细胞之间的相互作用是启动T细胞应答的前提条件。这种相互作用的分子本质仍有待充分阐明。我们在这项研究中报告,新鲜分离的小鼠脾脏DCs和骨髓来源的DCs在细胞表面以可溶性形式表达CD137。激活CD137可增加DCs分泌IL-6和IL-12。更重要的是,向未致敏小鼠体内注射抗CD137激动性单克隆抗体可增强DCs在体外响应同种异体抗原和一种名义抗原刺激T细胞增殖的能力。DC功能的这种增强不是通过激活T细胞介导的,因为在缺乏T细胞的RAG-1基因敲除小鼠中也观察到了这种效应。我们的研究结果表明CD137是参与调节DC功能的重要受体。