Yoshida Atsushi, Kohka Takahashi Hideo, Iwagaki Hiromi, Yoshino Tadashi, Morichika Toshihiko, Yokoyama Minori, Itoh Hideyuki, Mori Shuji, Akagi Tadaatsu, Nishibori Masahiro, Tanaka Noriaki
Department of Gastroenterological Surgery, Transplant and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, 2-5-1 Shikata-cho, Okayama 700-8558, Japan.
Naunyn Schmiedebergs Arch Pharmacol. 2002 Mar;365(3):181-6. doi: 10.1007/s00210-001-0518-6. Epub 2002 Feb 5.
IL-18 (0-100 ng/ml) specifically upregulated ICAM-1 expression on monocytes in human PBMC as demonstrated in our previous study. In the present study, we examined whether the synergistic upregulation of ICAM-1 occurred after the stimulation with the combination of IL-18 and IL-12 and whether the synergistic production of IFN-gamma was dependent on the interaction between ICAM-1 on monocytes and LFA-1 on NK/T cells. The effect of IL-12 on ICAM-1 expression on monocytes was marginal even at the highest concentration (100 ng/ml). However, in the presence of IL-12 (100 ng/ml), the expression of ICAM-1 induced by IL-18 was significantly enhanced as compared with that obtained by IL-18 alone. In addition to the expression of ICAM-1 on monocytes, IFN-gamma production was synergistically stimulated by IL-18 and IL-12. Anti-ICAM-1 and anti-LFA-1 Abs exhibited significant inhibitory effect on enhanced production of IFN-gamma by the combination of two cytokines, in particular, anti-ICAM-1 showing the complete inhibition. These results as a whole indicated that synergistic effect of IL-18 and IL-12 on IFN-gamma production in human PBMC is ascribed to the synergism of the effect of two cytokines on ICAM-1 expression on monocytes and that the subsequent ICAM-1/LFA-1 interaction plays an important role in the enhanced production of IFN-gamma.
如我们之前的研究所证明,白细胞介素-18(0-100纳克/毫升)可特异性上调人外周血单个核细胞中单核细胞上细胞间黏附分子-1(ICAM-1)的表达。在本研究中,我们检测了白细胞介素-18和白细胞介素-12联合刺激后是否会出现ICAM-1的协同上调,以及干扰素-γ的协同产生是否依赖于单核细胞上的ICAM-1与自然杀伤细胞/ T细胞上的淋巴细胞功能相关抗原-1(LFA-1)之间的相互作用。即使在最高浓度(100纳克/毫升)下,白细胞介素-12对单核细胞上ICAM-1表达的影响也很微小。然而,在存在白细胞介素-12(100纳克/毫升)的情况下,与单独使用白细胞介素-18相比,白细胞介素-18诱导的ICAM-1表达显著增强。除了单核细胞上ICAM-1的表达外,白细胞介素-18和白细胞介素-12还协同刺激干扰素-γ的产生。抗ICAM-1和抗LFA-1抗体对两种细胞因子联合增强干扰素-γ的产生具有显著抑制作用,尤其是抗ICAM-1显示出完全抑制作用。这些结果总体表明,白细胞介素-18和白细胞介素-12对人外周血单个核细胞中干扰素-γ产生的协同作用归因于两种细胞因子对单核细胞上ICAM-1表达的协同作用,并且随后的ICAM-1/LFA-1相互作用在增强干扰素-γ的产生中起重要作用。