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首页> 外文期刊>Cytokine >Polyriboinosinic-polyribocytidylic acid facilitates interleukin-6, and interleukin-8 secretion in human dermal fibroblasts via the JAK/STAT3 and p38 MAPK signal transduction pathways
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Polyriboinosinic-polyribocytidylic acid facilitates interleukin-6, and interleukin-8 secretion in human dermal fibroblasts via the JAK/STAT3 and p38 MAPK signal transduction pathways

机译:多吡吡吡吡吡吡啶鎓酰基酸促进白细胞介素-6,并通过JAK / STAT3和P38 MAPK信号转导途径促进白细胞介素-8在人皮肤成纤维细胞中分泌

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摘要

Polyriboinosinic-polyribocytidylic acid (polyl:C) is a viral dsRNA analoguethat promotes wounds healing, accelerates re-epithelialization, granulation and neovascularization, and induces pro-inflammatory cytokine release. Little is known about polyl:C mediated induction of inflammatory mediators in human dermal fibroblast (HDFs), which form the primary scaffold for epithelial cells covering the wound. Here, we found that polyl:C enhances IL-6 and IL-8 mRNA expression and induces of IL-6 and IL-8 production in a concentration-dependent and time-dependent manner in HDFs. PolyI:C treatment rapidly increased phosphorylation level of both STAT3 and p38 mitogen-activated protein kinase (MAPK). Moreover, pretreatment with AG490, a Janus kinase (JAK) inhibitor, inhibited polyl:C-induced STAT3 phosphorylation and subsequent IL-6 and IL-8 release. Conversely, pretreatment with SB203580, a selective inhibitor of p38 MAPK, blocked p38 MAPK phosphorylation and IL-6 and IL-8 expression. In conclusion, polyl:C induces IL-6 and IL-8 production in HDFs via the JAK/STAT3 and p38 MAPK signaling pathways.
机译:Polyriboinisinic-polyriby yidylic acid(polyl:c)是一种病毒DsRNA类似物,促进伤口愈合,加速重新上皮,造粒和新生血管形成,并诱导促炎细胞因子释放。关于聚合物的含量毫无少的:C介导的人类皮肤成纤维细胞(HDFS)中的炎症介质诱导,其为覆盖伤口的上皮细胞的主要支架。在这里,我们发现聚合物:C增强IL-6和IL-8 mRNA表达,并以浓度依赖性和时间依赖性的方式诱导IL-6和IL-8产生。 Polyi:C治疗迅速增加了STAT3和P38丝裂剂活化蛋白激酶(MAPK)的磷酸化水平。此外,用AG490,Janus激酶(Jak)抑制剂的预处理,抑制聚合物:C诱导的STAT3磷酸化和随后的IL-6和IL-8释放。相反,用SB203580进行预处理,P38 MAPK的选择性抑制剂,阻断P38 MAPK磷酸化和IL-6和IL-8表达。总之,聚物:C通过JAK / Stat3和P38 MAPK信号通路诱导HDFS中的IL-6和IL-8产生。

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