Fan X D, Goldberg M, Bloom B R
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461.
Proc Natl Acad Sci U S A. 1988 Jul;85(14):5122-5. doi: 10.1073/pnas.85.14.5122.
Interferon-gamma (IFN-gamma) regulates a variety of biological functions and is the principal lymphokine known to activate macrophages. In studies of the molecular mechanisms by which these cells are regulated by IFN-gamma, the transcriptional activation of an IFN-gamma-inducible gene, gamma.1, in human macrophage-like cell lines was examined. Transcription of this gene is rapidly induced by 0.1-1 unit of IFN-gamma. In addition, gamma.1 transcription is efficiently induced by phorbol 12-myristate 13-acetate, which is known to activate protein kinase C (PKC). Both stimulators of gamma.1 transcription induce the translocation of PKC from the cytosol of a membrane fraction. Two selective inhibitors of PKC, H7 and sphingosine, suppressed not only the induction of gamma.1 mRNA but transcription of HLA-DR by IFN-gamma as well. These findings establish that PKC plays a significant role in the signal transduction pathway leading to transcriptional activation of some IFN-gamma-regulated genes of cells of the mononuclear phagocyte lineage.
γ干扰素(IFN-γ)调节多种生物学功能,是已知可激活巨噬细胞的主要淋巴因子。在研究这些细胞受IFN-γ调节的分子机制时,检测了人巨噬细胞样细胞系中IFN-γ诱导基因γ.1的转录激活情况。该基因的转录可被0.1 - 1单位的IFN-γ迅速诱导。此外,佛波酯12-肉豆蔻酸酯13-乙酸酯(已知可激活蛋白激酶C(PKC))能有效诱导γ.1转录。γ.1转录的两种刺激物均可诱导PKC从膜部分的胞质溶胶中易位。PKC的两种选择性抑制剂H7和鞘氨醇不仅抑制γ.1 mRNA的诱导,还抑制IFN-γ诱导的HLA-DR转录。这些发现表明,PKC在导致单核吞噬细胞系细胞某些IFN-γ调节基因转录激活的信号转导途径中起重要作用。