Figueiredo F, Koerner T J, Adams D O
Department of Pathology, Duke University Medical Center, Durham, NC 27710.
J Immunol. 1989 Dec 1;143(11):3781-6.
The surface expression of class II MHC molecules (immune associated or Ia Ag) is an acquired and important property of macrophages. Recent evidence from several laboratories demonstrates that mRNA levels for class II genes reflect levels of surface expression. We have investigated the effects of agents that regulate Ia expression, either positively as IFN-gamma or negatively as bacterial LPS or maleylated proteins, on transcription of these genes. By using probes for I-A beta and I-E beta as representative class II MHC genes, we found that IFN-gamma induces transcription in murine peritoneal macrophages of I-A beta and of I-E beta as determined in nuclear run-on assays. The measured transcription peaked 6 to 10 h after administration of IFN-gamma to the macrophages. This augmented expression of transcription was markedly suppressed by administration of either LPS or maleylated protein to the macrophages. Collectively, the data indicate that regulation of transcription by either positive or negative stimuli, acting through surface receptors and binding sites, is a major mechanism for controlling the expression of class II MHC molecules in macrophages.
II类主要组织相容性复合体分子(免疫相关抗原或Ia抗原)的表面表达是巨噬细胞获得的一种重要特性。几个实验室最近的证据表明,II类基因的mRNA水平反映了表面表达水平。我们研究了正向调节Ia表达的因子(如干扰素-γ)或负向调节Ia表达的因子(如细菌脂多糖或马来酰化蛋白)对这些基因转录的影响。通过使用I-Aβ和I-Eβ探针作为代表性的II类主要组织相容性复合体基因,我们发现在核转录分析中,干扰素-γ可诱导小鼠腹腔巨噬细胞中I-Aβ和I-Eβ的转录。在向巨噬细胞施用干扰素-γ后6至10小时,测得的转录达到峰值。向巨噬细胞施用脂多糖或马来酰化蛋白可显著抑制这种增强的转录表达。总体而言,数据表明,通过表面受体和结合位点起作用的正向或负向刺激对转录的调节是控制巨噬细胞中II类主要组织相容性复合体分子表达的主要机制。