Hu Xiaoyu, Paik Paul K, Chen Janice, Yarilina Anna, Kockeritz Lisa, Lu Theresa T, Woodgett James R, Ivashkiv Lionel B
Arthritis and Tissue Degeneration Program, Hospital for Special Surgery, Weill Graduate School of Medical Sciences of Cornell University, New York, New York 10021, USA.
Immunity. 2006 May;24(5):563-74. doi: 10.1016/j.immuni.2006.02.014.
The control of IL-10 production and mechanisms that mediate synergy between IFN-gamma and TLR ligands are not well understood. We report that IFN-gamma augments induction of TNFalpha by TLR ligands, immune complexes, and zymosan by suppressing IL-10 production and thereby interrupting Stat3-mediated feedback inhibition. IFN-gamma altered TLR2-induced signal transduction by increasing GSK3 activity and suppressing MAPK activation, leading to diminished IL-10 production. Inhibition of GSK3 or ablation of the GSK3beta gene ameliorated TLR2-induced peritonitis and arthritis. IFN-gamma suppressed the activity of CREB and AP-1, transcription factors that induce IL-10 expression and are regulated in part by MAPKs and GSK3. These results yield insight into mechanisms by which IFN-gamma regulates IL-10 production and TLR2-mediated inflammatory responses and identify inhibition of CREB and AP-1 as part of the macrophage response to IFN-gamma. GSK3 and CREB/AP-1 are key players in integrating IFN-gamma and TLR2 responses in innate immunity and inflammation.
目前对白细胞介素-10(IL-10)产生的控制以及介导干扰素-γ(IFN-γ)与Toll样受体(TLR)配体之间协同作用的机制尚不清楚。我们报告称,IFN-γ通过抑制IL-10的产生,从而中断信号转导和转录激活因子3(Stat3)介导的反馈抑制,增强了TLR配体、免疫复合物和酵母聚糖对肿瘤坏死因子α(TNFα)的诱导作用。IFN-γ通过增加糖原合成酶激酶3(GSK3)的活性并抑制丝裂原活化蛋白激酶(MAPK)的激活,改变了TLR2诱导的信号转导,导致IL-10产生减少。抑制GSK3或敲除GSK3β基因可改善TLR2诱导的腹膜炎和关节炎。IFN-γ抑制了cAMP反应元件结合蛋白(CREB)和激活蛋白-1(AP-1)的活性,这两种转录因子可诱导IL-10表达,并且部分受MAPKs和GSK3的调控。这些结果有助于深入了解IFN-γ调节IL-10产生和TLR2介导的炎症反应的机制,并确定抑制CREB和AP-1是巨噬细胞对IFN-γ反应的一部分。GSK3和CREB/AP-1是在先天免疫和炎症中整合IFN-γ和TLR2反应的关键因素。