Liu Lei, Wang Yun, Fan Yi, Li Chang-Lin, Chang Zong-Liang
Laboratory of Molecular Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, PR China.
J Interferon Cytokine Res. 2004 Jun;24(6):334-42. doi: 10.1089/107999004323142196.
Interferon-gamma (IFN-gamma) is a macrophage-activating cytokine that serves critical functions in innate and adaptive immunity and is thought to be mediated by the Jak-Stat signaling pathway. The present study establishes for the first time that cyclic adenosine monophosphate, protein kinase A, and cAMP response element-binding protein (cAMP/PKA/CREB) are coregulators of the IFN-gamma signaling pathway. Experimental data indicate that exogenous IFN-gamma stimulated cAMP accumulation and PKA activation in time-dependent and dose-dependent manners in murine peritoneal macrophages. Moreover, IFN-gamma stimulated CREB phosphorylation and CREB DNA binding, which could be significantly attenuated by PKA inhibition with H89. It appears that a novel cAMP/PKA/CREB signaling pathway is activated by IFN-gamma in macrophages, suggesting that an alternate signaling pathway exists in macrophages in response to IFN-gamma.
γ-干扰素(IFN-γ)是一种巨噬细胞激活细胞因子,在固有免疫和适应性免疫中发挥关键作用,并且被认为是由Jak-Stat信号通路介导的。本研究首次证实环磷酸腺苷、蛋白激酶A和环磷酸腺苷反应元件结合蛋白(cAMP/PKA/CREB)是IFN-γ信号通路的共调节因子。实验数据表明,外源性IFN-γ以时间和剂量依赖性方式刺激小鼠腹腔巨噬细胞中cAMP的积累和PKA的激活。此外,IFN-γ刺激CREB磷酸化和CREB与DNA结合,而用H89抑制PKA可显著减弱这种作用。看来IFN-γ在巨噬细胞中激活了一条新的cAMP/PKA/CREB信号通路,这表明巨噬细胞中存在一条响应IFN-γ的替代信号通路。