Kawada N, Mizoguchi Y, Kobayashi K, Morisawa S, Monna T, Yamamoto S
Third Department of Internal Medicine, Osaka City University Medical School, Japan.
Liver. 1991 Feb;11(1):42-7. doi: 10.1111/j.1600-0676.1991.tb00489.x.
When mononuclear phagocytes, including Kupffer cells, are activated by various agents, they synthesize and release cytokines such as interleukin 1 (IL-1) and tumor necrosis factor (TNF). In this study, we examined the effect of in vitro Kupffer cell activation by recombinant murine interferon gamma (IFN gamma) on IL-1 and TNF secretion. IFN gamma enhanced TNF production in the presence or absence of lipopolysaccharide (LPS), but suppressed IL-1 production by Kupffer cells. Because IFN gamma also stimulated prostaglandin E2 (PGE2) production, the effect of indomethacin, which is an inhibitor of cyclooxygenase and which inhibits PGE2 biosynthesis, on IL-1 and TNF production by Kupffer cells was examined. As a result, indomethacin enhanced TNF production by Kupffer cells, but had no effect on IL-1 synthesis. These results suggested that IFN gamma modulates the production of IL-1 and TNF by Kupffer cells through different mechanisms.
当包括库普弗细胞在内的单核吞噬细胞被各种因子激活时,它们会合成并释放细胞因子,如白细胞介素1(IL-1)和肿瘤坏死因子(TNF)。在本研究中,我们检测了重组鼠γ干扰素(IFNγ)体外激活库普弗细胞对IL-1和TNF分泌的影响。无论有无脂多糖(LPS),IFNγ均可增强TNF的产生,但抑制库普弗细胞产生IL-1。由于IFNγ还刺激前列腺素E2(PGE2)的产生,因此检测了环氧化酶抑制剂吲哚美辛对库普弗细胞产生IL-1和TNF的影响,吲哚美辛可抑制PGE2的生物合成。结果,吲哚美辛增强了库普弗细胞产生TNF的能力,但对IL-1的合成没有影响。这些结果表明,IFNγ通过不同机制调节库普弗细胞产生IL-1和TNF。