Kim H S, Shin D H, Kim S K
Department of Microbiology, College of Medicine, Yeungnam University, Taegu, Korea.
J Korean Med Sci. 1999 Oct;14(5):480-6. doi: 10.3346/jkms.1999.14.5.480.
Chemokine KC has been considered to be a murine homologue of human GRO/MGSA and was identified as chemoattractant for monocytes and neutrophils. This study examined the expression of KC mRNA in thioglycollate-elicited mouse peritoneal macrophages that were stimulated in vitro with Candida albicans (CA). Also examined were the inhibitory effects of IL-10 on the CA-induced expression of KC gene by Northern blot analysis. CA was found to induce chemokine gene expression in a gene-specific manner, CXC chemokine IP-10 mRNA expression was not detected in CA-stimulated macrophages. Maximum KC mRNA expression was observed approximately 2 hr after adding CA. The inhibitory action of IL-10 to CA-induced KC mRNA expression on mouse peritoneal macrophages was independent on concentration and stimulation time of IL-10 and was observed approximately one hour after adding IL-10 and CA simultaneously. IL-10 produced a decrease in the stability of KC mRNA, and CA-stimulated macrophages with cycloheximide blocked the suppressive effect of IL-10. These results suggest that CA also induces chemokine KC from macrophages, and IL-10 acts to destabilize CA-induced KC mRNA and de novo synthesis of an intermediate protein is a part of the IL-10 suppressive mechanism.
趋化因子KC被认为是人类GRO/MGSA的小鼠同源物,并被鉴定为单核细胞和中性粒细胞的趋化因子。本研究检测了用白色念珠菌(CA)体外刺激的巯基乙酸盐诱导的小鼠腹腔巨噬细胞中KC mRNA的表达。还通过Northern印迹分析检测了IL-10对CA诱导的KC基因表达的抑制作用。发现CA以基因特异性方式诱导趋化因子基因表达,在CA刺激的巨噬细胞中未检测到CXC趋化因子IP-10 mRNA表达。添加CA后约2小时观察到KC mRNA表达达到最大值。IL-10对小鼠腹腔巨噬细胞中CA诱导的KC mRNA表达的抑制作用与IL-10的浓度和刺激时间无关,在同时添加IL-10和CA后约1小时观察到。IL-10使KC mRNA的稳定性降低,用放线菌酮刺激的巨噬细胞可阻断IL-10的抑制作用。这些结果表明,CA也可从巨噬细胞诱导趋化因子KC,IL-10可使CA诱导的KC mRNA不稳定,中间蛋白的从头合成是IL-10抑制机制的一部分。