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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Involvement of P2Y11 receptor in IFN-γ-induced IL-6 production in human keratinocytes
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Involvement of P2Y11 receptor in IFN-γ-induced IL-6 production in human keratinocytes

机译:P2Y11受体参与人角质形成细胞中IFN-γ诱导的IL-6产生。

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摘要

Extracellular ATP and P2 receptors are reported to be involved in interleukin-6 (IL-6) production by human keratinocytes, but the role of extracellular ATP in cytokine-induced IL-6 production remains unclear. In this study, we investigated the involvement of various P2 receptors in IL-6 production induced by the Th1 cytokine interferon-gamma (IFN-γ) in a human keratinocyte cell line, HaCaT. IFN-γ increased IL-6 production in HaCaT cells. A non-selective antagonist of P2Y receptors (suramin), a selective P2Y11 receptor antagonist (NF157), ecto-nucleotidase (apyrase), and a soluble adenylate cyclase inhibitor (KH7) all inhibited IL-6 production. It was further confirmed that ATP was released from HaCaT cells stimulated with IFN-γ. These results suggest that extracellular ATP and P2Y11 receptor are involved in IFN-γ-induced IL-6 production. Knockdown of P2Y11 receptor suppressed IL-6 production, strongly supporting this idea. In conclusion, these data demonstrate that P2Y11 receptor mediates IFN-γ-induced IL-6 production in human keratinocytes, and suggest the importance of purinergic signaling in IFN-γ-induced skin inflammatory conditions, such as psoriasis.
机译:据报道细胞外ATP和P2受体参与人角质形成细胞的白介素6(IL-6)产生,但是细胞外ATP在细胞因子诱导的IL-6产生中的作用仍不清楚。在这项研究中,我们调查了人类角质形成细胞系HaCaT中Th1细胞因子干扰素-γ(IFN-γ)诱导的IL-6产生中各种P2受体的参与。 IFN-γ增加了HaCaT细胞中IL-6的产生。 P2Y受体(苏拉明)的非选择性拮抗剂,选择性P2Y11受体拮抗剂(NF157),胞外核苷酸酶(apyrase)和可溶性腺苷酸环化酶抑制剂(KH7)均抑制IL-6的产生。进一步证实ATP是从IFN-γ刺激的HaCaT细胞中释放的。这些结果表明,细胞外ATP和P2Y11受体参与IFN-γ诱导的IL-6产生。抑制P2Y11受体抑制了IL-6的产生,有力地支持了这一想法。总之,这些数据表明,P2Y11受体介导了人角质形成细胞中IFN-γ诱导的IL-6的产生,并表明嘌呤能信号在IFN-γ诱导的皮肤炎性疾病(如牛皮癣)中的重要性。

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