Kim H S, Armstrong D, Hamilton T A, Tebo J M
Department of Immunology, Lerner Research Institute, Cleveland Clinic Foundation, Ohio 44195, USA.
J Leukoc Biol. 1998 Jul;64(1):33-9. doi: 10.1002/jlb.64.1.33.
This study examines the mechanism of interleukin-10 (IL-10)-mediated suppression of KC chemokine gene expression in mouse macrophages. Suppression of KC mRNA levels by IL-10 occurred late in the time course of response to lipopolysaccharide (LPS). Equivalent IL-10-mediated suppression was observed when the agent was added 1 h before, simultaneous with, or 1 h after LPS. IL-10 did not inhibit KC gene transcription but rather produced a decrease in the stability of KC mRNA. The suppressive action of IL-10 was prevented in macrophages that were also treated with inhibitors of protein synthesis even when added 2 h after LPS and IL-10. These results suggest that IL-10 acts to destabilize LPS-induced KC mRNA through a process that depends on coincident KC mRNA translation.
本研究探讨白细胞介素-10(IL-10)介导的对小鼠巨噬细胞中KC趋化因子基因表达的抑制机制。IL-10对KC mRNA水平的抑制发生在对脂多糖(LPS)应答过程的后期。当在LPS之前1小时、与LPS同时或在LPS之后1小时添加该因子时,观察到等效的IL-10介导的抑制作用。IL-10不抑制KC基因转录,而是导致KC mRNA稳定性降低。即使在LPS和IL-10之后2小时添加,用蛋白质合成抑制剂处理的巨噬细胞中IL-10的抑制作用也被阻止。这些结果表明,IL-10通过一个依赖于同时进行的KC mRNA翻译的过程,使LPS诱导的KC mRNA不稳定。