首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Ma Huang Tang Suppresses the Production and Expression of Inflammatory Chemokines via Downregulating STAT1 Phosphorylation in HaCaT Keratinocytes
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Ma Huang Tang Suppresses the Production and Expression of Inflammatory Chemokines via Downregulating STAT1 Phosphorylation in HaCaT Keratinocytes

机译:马皇堂通过下调HaCaT角质形成细胞中STAT1磷酸化来抑制炎症趋化因子的产生和表达。

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Ma huang tang (MHT) is a traditional herbal medicine comprising six medicinal herbs and is used to treat influenza-like illness. However, the effects of MHT on inflammatory skin diseases have not been verified scientifically. We investigated determining the inhibitory effects of MHT against inflammation responses in skin using HaCaT human keratinocyte cells. We found that MHT suppressed production of thymus and activation-regulated chemokine (TARC/CCL17), macrophage-derived chemokine (MDC/CCL22), regulated on activation of normal T-cell expressed and secreted (RANTES/CCL5), and interleukin-8 (IL-8) in tumor necrosis factor-? (TNF-?) and interferon-?- (IFN-?-) stimulated HaCaT cells. Consistently, MHT suppressed the mRNA expression of TARC, MDC, RANTES, and IL-8 in TNF-? and IFN-?-stimulated cells. Additionally, MHT inhibited TNF-? and IFN-?-stimulated signal transducer and activator of transcription 1 (STAT1) phosphorylation in a dose-dependent manner and nuclear translocation in HaCaT cells. Our finding indicates that MHT inhibits production and expression of inflammatory chemokines in the stimulated keratinocytes by downregulating STAT1 phosphorylation, suggesting that MHT may be a possible therapeutic agent for inflammatory skin diseases.
机译:马皇堂(MHT)是包括六种草药的传统草药,用于治疗类似流感的疾病。但是,MHT对炎症性皮肤病的作用尚未得到科学证实。我们调查了使用HaCaT人角质形成细胞确定MHT对皮肤炎症反应的抑制作用。我们发现MHT抑制了胸腺的产生和激活调节的趋化因子(TARC / CCL17),巨噬细胞衍生的趋化因子(MDC / CCL22),对正常T细胞表达和分泌的激活(RANTES / CCL5)和IL-8的调控(IL-8)在肿瘤坏死因子中? (TNF-α)和干扰素-α-(IFN-α-)刺激的HaCaT细胞。一致地,MHT抑制TNF-α中TARC,MDC,RANTES和IL-8的mRNA表达。和IFN-α刺激的细胞。另外,MHT抑制TNF-α。以及IFN-α刺激的信号转导和转录激活因子1(STAT1)的磷酸化,其剂量依赖性和HaCaT细胞中的核易位。我们的发现表明,MHT通过下调STAT1磷酸化抑制刺激的角质形成细胞中炎症趋化因子的产生和表达,这表明MHT可能是炎症性皮肤病的一种可能的治疗剂。

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