MHC II类抗原表达的调控。肿瘤坏死因子-α对干扰素-γ诱导的HLA-DR和Ia表达的相反作用取决于细胞的成熟和分化阶段。
Regulation of MHC class II antigen expression. Opposing effects of tumor necrosis factor-alpha on IFN-gamma-induced HLA-DR and Ia expression depends on the maturation and differentiation stage of the cell.
作者信息
Watanabe Y, Jacob C O
机构信息
Syntex Research, Palo Alto, CA 94303.
出版信息
J Immunol. 1991 Feb 1;146(3):899-905.
MHC class II induction by cytokines has been suggested to play a major role in the initiation and propagation of immune and autoimmune processes. TNF-alpha has been found both to enhance and also to inhibit IFN-gamma-induced MHC class II expression. In the present studies, the effect of TNF-alpha on IFN-gamma induced MHC class II expression was tested in various cell lines. On the basis of the data, we propose that, depending on the stage of differentiation and maturation of the cells, TNF-alpha might synergize or antagonize the affects of IFN-gamma on the regulation of MHC class II expression. Thus, in immature cells such as HL-60 or THP-1, TNF-alpha enhances IFN-gamma-induced class II expression. However, when differentiation was induced in these cells by TPA or IFN-gamma, the additive effect of TNF-alpha on the IFN-gamma induced DR expression was eliminated. Furthermore, TNF-alpha down-regulates the IFN-gamma-induced class II expression in differentiated cells such as human skin fibroblasts or activated macrophages. In bone marrow cells induced to differentiate in vitro, TNF-alpha decreased the IFN-gamma-induced MHC class II expression in a maturation-dependent fashion. These results provide a rational explanation for the conflicting reports regarding the effect of TNF-alpha on IFN-gamma-induced class II expression. But more importantly they may be relevant to the biologic function of TNF-alpha. Thus, we show that TNF-alpha-treated mice have reduced level of Ia expression on peritoneal macrophages and in vivo treatment with TNF-alpha antagonizes the ability of IFN-gamma to induce class II expression on these macrophages.
细胞因子诱导的MHC II类分子被认为在免疫和自身免疫过程的启动和传播中起主要作用。已发现肿瘤坏死因子-α(TNF-α)既能增强也能抑制干扰素-γ(IFN-γ)诱导的MHC II类分子表达。在本研究中,在各种细胞系中测试了TNF-α对IFN-γ诱导的MHC II类分子表达的影响。基于这些数据,我们提出,根据细胞分化和成熟的阶段,TNF-α可能协同或拮抗IFN-γ对MHC II类分子表达调控的影响。因此,在未成熟细胞如HL-60或THP-1中,TNF-α增强IFN-γ诱导的II类分子表达。然而,当用佛波酯(TPA)或IFN-γ诱导这些细胞分化时,TNF-α对IFN-γ诱导的DR表达的加成作用被消除。此外,TNF-α下调分化细胞如人皮肤成纤维细胞或活化巨噬细胞中IFN-γ诱导的II类分子表达。在体外诱导分化的骨髓细胞中,TNF-α以成熟依赖的方式降低IFN-γ诱导的MHC II类分子表达。这些结果为关于TNF-α对IFN-γ诱导的II类分子表达影响的相互矛盾的报道提供了合理的解释。但更重要的是,它们可能与TNF-α的生物学功能相关。因此,我们表明,用TNF-α处理的小鼠腹膜巨噬细胞上Ia表达水平降低,并且在体内用TNF-α处理可拮抗IFN-γ诱导这些巨噬细胞上II类分子表达的能力。