Ojo-Amaize E A, Rubalcava B, Avery T L, Cottam H B, Matsumoto S S, Jolley W B, Robins R K
ICN Nucleic Acid Research Institute, Costa Mesa, CA 92626.
Immunol Lett. 1990 Jan;23(3):173-8. doi: 10.1016/0165-2478(90)90187-u.
The capacity of certain guanine ribonucleosides (modified at the 7 and/or 8 positions) to enhance the respiratory burst of murine peritoneal phagocytes was evaluated. The results show that 8-mercaptoguanosine, 8-bromoguanosine, 7-methyl-8-oxoguanosine and 7-thia-8-oxoguanosine, when injected intraperitoneally into mice, induced peritoneal phagocytes to generate reactive oxygen species as early as 1 h after injection. In vivo administration of the nucleosides induced higher levels of phagocyte activation than in vitro treatment with the same nucleosides. However, the addition of interferon alpha/beta in vitro significantly increased the magnitude of phagocyte activation by the nucleosides, suggesting an important role for cytokines/lymphokines in the nucleoside-induced phagocyte activation in vivo. Furthermore, pre-treatment of phagocytes in vitro with Bordetella pertussis toxin, before treatment with the guanosines, inhibited their capacity to induce the respiratory burst. These observations establish these low-molecular-weight compounds as interesting probes for the study of stimulus-response coupling in phagocytes.
评估了某些(在7和/或8位修饰的)鸟嘌呤核糖核苷增强小鼠腹膜吞噬细胞呼吸爆发的能力。结果表明,8-巯基鸟苷、8-溴鸟苷、7-甲基-8-氧代鸟苷和7-硫杂-8-氧代鸟苷腹腔注射到小鼠体内后,早在注射后1小时就诱导腹膜吞噬细胞产生活性氧。核苷的体内给药比用相同核苷进行体外处理诱导的吞噬细胞活化水平更高。然而,体外添加α/β干扰素显著增加了核苷诱导的吞噬细胞活化程度,表明细胞因子/淋巴因子在核苷诱导的体内吞噬细胞活化中起重要作用。此外,在用鸟苷处理之前,体外先用百日咳博德特氏菌毒素预处理吞噬细胞,可抑制其诱导呼吸爆发的能力。这些观察结果确立了这些低分子量化合物作为研究吞噬细胞刺激-反应偶联的有趣探针。