首页> 美国卫生研究院文献>Journal of Innate Immunity >The IL-13 Receptor-α1 Chain Is Essential for Induction of theAlternative Macrophage Activation Pathway by IL-13 but not IL-4
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The IL-13 Receptor-α1 Chain Is Essential for Induction of theAlternative Macrophage Activation Pathway by IL-13 but not IL-4

机译:IL-13受体-α1链对于诱导细胞凋亡至关重要IL-13替代IL-4的替代性巨噬细胞激活途径

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摘要

Macrophages co-express both the IL-2Rγ chain (γc) and IL-13Rα1. These receptor chains can heterodimerize with IL-4Rα to form type-I or type-II IL-4 receptor complexes, respectively. We used macrophages derived from Il2rg and Il13ra1 knockout mice to evaluate the requirements for these receptor chains for induction of the alternative macrophage activation (AMA) pathway by IL-4 and IL-13. Absence of γc significantly decreased activation of STAT6 by IL-4 but not IL-13. However, although activation of STAT6 by IL-4 was markedly reduced in γc KO macrophages, it was not abolished, indicating that IL-4 can still signal through type-II IL-4 receptors via the IL-13Rα1 chain. IL-13 failed to activate STAT6 in macrophages derived from Il13ra1 KO mice; however, these cells remained fully responsive to IL-4. The inability of IL-13 but not IL-4 to signal in Il13ra1−/− macrophages correlated with the inability of IL-13 but not IL-4 to induce expression of genes such as Arg1, Retnla and Ccl11 that are characteristically expressed by alternatively activated macrophages. In addition, IL-13 but not IL-4 failed to induce membrane fusion and giant cell formation by Il13ra1 KO macrophages. These findings demonstrate that the IL-13Rα1 chain is essential forinduction of the AMA pathway by IL-13 but not IL-4.
机译:巨噬细胞共表达IL-2Rγ链(γc)和IL-13Rα1。这些受体链可以与IL-4Rα异源二聚体形成I型或II型IL-4受体复合物。我们使用衍生自Il2rg和Il13ra1敲除小鼠的巨噬细胞来评估这些受体链对IL-4和IL-13诱导替代巨噬细胞激活(AMA)途径的需求。缺乏γc会显着降低IL-4激活STAT6的激活,但不会降低IL-13的激活。然而,尽管在γc KO巨噬细胞中IL-4对STAT6的激活显着降低,但并未消除,表明IL-4仍然可以通过IL-13Rα1链通过II型IL-4受体发出信号。 IL-13未能激活源自Il13ra1 KO小鼠的巨噬细胞中的STAT6。但是,这些细胞仍然对IL-4完全应答。 IL-13不能在Il13ra1 -/-巨噬细胞中发信号,而IL-13却不能IL-4诱导诸如Arg1,Retnla和由交替激活的巨噬细胞特征性表达的Ccl11。另外,IL-13而不是IL-4不能通过Il13ra1 KO巨噬细胞诱导膜融合和巨细胞形成。这些发现表明,IL-13Rα1链对于IL-13而非IL-4诱导AMA途径。

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