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首页> 外文期刊>Nature Communications >Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway
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Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway

机译:IL-17和D-resolvins通过GSK-3β-C/EBPβ途径对内皮Del-1表达的拮抗作用

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摘要

Del-1 is an endothelial cell-secreted anti-inflammatory protein. In humans and mice, Del-1 expression is inversely related to that of IL-17, which inhibits Del-1 through hitherto unidentified mechanism(s). Here we show that IL-17 downregulates human endothelial cell expression of Del-1 by targeting a critical transcription factor, C/EBPβ. Specifically, IL-17 causes GSK-3β-dependent phosphorylation of C/EBPβ, which is associated with diminished C/EBPβ binding to the Del-1 promoter and suppressed Del-1 expression. This inhibitory action of IL-17 can be reversed at the GSK-3β level by PI3K/Akt signalling induced by D-resolvins. The biological relevance of this regulatory network is confirmed in a mouse model of inflammatory periodontitis. Intriguingly, resolvin-D1 (RvD1) confers protection against IL-17-driven periodontal bone loss in a Del-1-dependent manner, indicating an RvD1-Del-1 axis against IL-17-induced pathological inflammation. The dissection of signalling pathways regulating Del-1 expression provides potential targets to treat inflammatory diseases associated with diminished Del-1 expression, such as periodontitis and multiple sclerosis.
机译:Del-1是一种内皮细胞分泌的抗炎蛋白。在人类和小鼠中,Del-1的表达与IL-17的表达呈反相关,后者通过迄今未知的机制抑制Del-1。在这里,我们显示IL-17通过靶向关键转录因子C /EBPβ来下调人类内皮细胞Del-1的表达。具体而言,IL-17引起C /EBPβ的GSK-3β依赖性磷酸化,这与与Del-1启动子结合的C /EBPβ减少和Del-1表达的抑制有关。 IL-17的这种抑制作用可以通过D-resolvins诱导的PI3K / Akt信号传导在GSK-3β水平上逆转。在炎症性牙周炎的小鼠模型中证实了该调节网络的生物学相关性。有趣的是,resolvin-D1(RvD1)以Del-1依赖性方式赋予针对IL-17驱动的牙周骨丢失的保护作用,表明RvD1-Del-1轴可抵抗IL-17诱导的病理性炎症。调节Del-1表达的信号通路的解剖提供了潜在的靶标,以治疗与Del-1表达降低有关的炎性疾病,例如牙周炎和多发性硬化。

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