Fukao T, Matsuda S, Koyasu S
Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan.
J Immunol. 2000 Jan 1;164(1):64-71. doi: 10.4049/jimmunol.164.1.64.
Mouse splenic dendritic cells (DCs) produce IFN-gamma in response to IL-12. In the present study, we analyzed effects of Th1 and Th2 cytokines on IFN-gamma production by DCs. IL-18 produced by DCs and macrophages acts in an autocrine manner and augments IL-12-induced IFN-gamma production by DCs as also observed in T and NK cells. Surprisingly, IL-4, a Th2 cytokine, also acts synergistically with IL-12 on IFN-gamma production by DCs. In addition, IL-4 markedly enhances IFN-gamma production when DCs are stimulated through CD40 or MHC class II. These results indicate that both Th1 and Th2 cytokines act on DCs during T cell-DC interaction upon Ag presentation. p38 mitogen-activated protein kinase is constitutively activated in mature DCs and is required for IFN-gamma production by DCs. IL-18 but not IL-4 or IL-12 further activates the p38 mitogen-activated protein kinase activity, suggesting that IL-4 and IL-18 enhance IFN-gamma production through distinct intracellular signal transduction pathways in DCs.
小鼠脾脏树突状细胞(DCs)在受到白细胞介素-12(IL-12)刺激时会产生γ干扰素(IFN-γ)。在本研究中,我们分析了辅助性T细胞1型(Th1)和辅助性T细胞2型(Th2)细胞因子对DCs产生IFN-γ的影响。DCs和巨噬细胞产生的IL-18以自分泌方式发挥作用,并增强IL-12诱导的DCs产生IFN-γ,这在T细胞和自然杀伤(NK)细胞中也有观察到。令人惊讶的是,Th2细胞因子IL-4在DCs产生IFN-γ方面也与IL-12协同发挥作用。此外,当通过CD40或主要组织相容性复合体II类(MHC II类)刺激DCs时,IL-4会显著增强IFN-γ的产生。这些结果表明,在抗原呈递过程中T细胞与DCs相互作用期间,Th1和Th2细胞因子均作用于DCs。p38丝裂原活化蛋白激酶在成熟DCs中持续激活,并且是DCs产生IFN-γ所必需的。IL-18而非IL-4或IL-12会进一步激活p38丝裂原活化蛋白激酶活性,这表明IL-4和IL-18通过DCs中不同的细胞内信号转导途径增强IFN-γ的产生。