Cao H, Wolff R G, Meltzer M S, Crawford R M
Department of Cellular Immunology, Walter Reed Army Institute of Research, Washington, DC 20307-5100.
J Immunol. 1989 Dec 1;143(11):3524-31.
Initiation of an immune response depends upon expression of class II MHC determinants on plasma membranes of APC. Murine peritoneal macrophages treated with either rIFN-gamma or rIL-4 display significantly more class II MHC determinants than untreated control cells. Analysis of the induction of macrophage Ia Ag by these cytokines showed considerable quantitative and qualitative differences. Maximal levels of Ia Ag induced in macrophages and detected by ELISA after IL-4 treatment at 48 h was about 80% of that induced by IFN-gamma. However, the frequency of Ia+ cells in replicate macrophage populations cultured for 48 h in excess concentrations of cytokine was 60 to 80% with IFN-gamma, 30 to 40% with IL-4, and 5% with medium alone. Thus, the subpopulation of macrophages able to respond to IL-4 for induction of Ia Ag expression was less than that able to respond to IFN-gamma. Expression of Ia Ag on macrophages continuously exposed to IFN-gamma was maximal at 48 h and remained at this high level through 6 days. Maximal Ia Ag expression for IL-4-treated cells was also detected at 48 h, but was not sustained with time in culture, and returned to base line by 4 days. A similar time course for levels of Ia-specific message in macrophages at various times after IFN-gamma and IL-4 treatment was detected by Northern dot blot analysis. Loss of Ia mRNA and Ag with time in culture in the IL-4 treated cells was not due to macrophage cell death, depletion of active cytokine, or presence of fluid-phase inhibitors. IL-4 unresponsive cells were fully capable of maximal response to IFN-gamma for Ia Ag induction. These findings suggest that IL-4 and IFN-gamma induce class II MHC determinants through different mechanisms which may provide discrete regulatory control of APC function.
免疫反应的启动取决于抗原呈递细胞(APC)质膜上II类主要组织相容性复合体(MHC)决定簇的表达。用重组干扰素-γ(rIFN-γ)或重组白细胞介素-4(rIL-4)处理的小鼠腹腔巨噬细胞比未处理的对照细胞显示出明显更多的II类MHC决定簇。对这些细胞因子诱导巨噬细胞Ia抗原的分析显示出相当大的数量和质量差异。用酶联免疫吸附测定(ELISA)在48小时检测到白细胞介素-4处理后巨噬细胞中诱导的Ia抗原的最大水平约为干扰素-γ诱导水平的80%。然而,在过量细胞因子浓度下培养48小时的重复巨噬细胞群体中,Ia+细胞的频率在干扰素-γ处理时为60%至80%,白细胞介素-4处理时为30%至40%,单独培养基处理时为5%。因此,能够对白细胞介素-4作出反应以诱导Ia抗原表达的巨噬细胞亚群少于能够对干扰素-γ作出反应的亚群。持续暴露于干扰素-γ的巨噬细胞上Ia抗原的表达在48小时时达到最大值,并在6天内保持在这一高水平。白细胞介素-4处理细胞的最大Ia抗原表达也在48小时时检测到,但在培养过程中未随时间持续,到4天时恢复到基线水平。通过Northern斑点印迹分析检测到干扰素-γ和白细胞介素-4处理后不同时间巨噬细胞中Ia特异性信使水平的类似时间进程。在白细胞介素-4处理的细胞中,培养过程中Ia信使核糖核酸(mRNA)和抗原随时间的丧失不是由于巨噬细胞死亡、活性细胞因子耗竭或液相抑制剂的存在。白细胞介素-4无反应性细胞完全能够对干扰素-γ诱导Ia抗原作出最大反应。这些发现表明,白细胞介素-4和干扰素-γ通过不同机制诱导II类MHC决定簇,这可能为APC功能提供离散的调节控制。