Murray P J
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Biochem Soc Trans. 2006 Dec;34(Pt 6):1028-31. doi: 10.1042/BST0341028.
IL-1O (interleukin-10) negatively regulates inflammation through a mechanism that blocks the expression of pro-inflammatory genes encoding cytokines, chemokines, cell-surface molecules and other molecules required for the full activation of the innate and adaptive immune responses. The signalling pathway used by the IL-10 receptor to generate the anti-inflammatory response requires STAT3 (signal transducer and activator of transcription 3) and is indirect. Thus STAT3 activates other genes whose task is to selectively control transcription of inflammatory targets. Here, I summarize current knowledge of the key features of IL-10 signalling and make predictions concerning the mechanism of IL-10 at the level of inflammatory genes. Understanding IL-10 signalling should be a gateway to the development of broadly acting anti-inflammatory agents.
白细胞介素-10(IL-10)通过一种机制对炎症进行负调控,该机制可阻断编码细胞因子、趋化因子、细胞表面分子以及先天和适应性免疫反应完全激活所需的其他分子的促炎基因的表达。IL-10受体用于产生抗炎反应的信号通路需要信号转导及转录激活因子3(STAT3),且是间接的。因此,STAT3激活其他基因,这些基因的任务是选择性地控制炎症靶点的转录。在此,我总结了目前关于IL-10信号传导关键特征的知识,并对IL-10在炎症基因水平的作用机制进行了预测。了解IL-10信号传导应该是开发广泛作用的抗炎药物的一个途径。