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Phenotypic and functional maturation of murine dendritic cells (DCs) induced by purified Glycyrrhizin (GL)

机译:纯化的甘草甜素(GL)诱导的小鼠树突状细胞(DC)的表型和功能成熟

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The aim of this study is to investigate phenotypic and functional modulation of murine dendritic cells (DCs) with use of purified Glycyrrhizin (GL). These impacts of GL on DCs both from bone marrow derived DCs and established DC cell 2.4 were assessed with conventional scanning electron microscopy (SEM), flow cytometry (FCM), transmission electron microscopy (TEM), cytochemistry assay, FITC-dextran, bio-assay and enzyme linked immunosorbent assay (ELISA). We found that the purified GL induced phenotypic maturation as evidenced by increased expression of CD86, CD40, CD80, CD83 and major histocompatibility complex II (MHC II). The functional tests showed the activity of acidic phosphatase (ACP) inside the DCs2.4 cells were down- regulated after treatment with GL (which occurs when phagocytosis of DCs2.4 cells were decreased). Finally, we proved that GL increased the production of IL-12, IL-10 and decreased the production of tumor necrosis factor alpha (TNF-α). These data indicated that GL could promote maturation of DCs and this adjuvant-like activity may have potential therapeutic value. It is therefore concluded that GL could exert positive modulation on murine DCs.
机译:这项研究的目的是研究使用纯化的甘草甜素(GL)的小鼠树突状细胞(DC)的表型和功能调节。通过常规扫描电子显微镜(SEM),流式细胞仪(FCM),透射电子显微镜(TEM),细胞化学分析,FITC-葡聚糖,生物技术对GL对来自骨髓来源的DC和建立的DC细胞2.4的DC的这些影响进行了评估。检测和酶联免疫吸附测定(ELISA)。我们发现纯化的GL诱导表型成熟,如CD86,CD40,CD80,CD83和主要组织相容性复合物II(MHC II)的表达增加所证明。功能测试表明,用GL处理后DCs2.4细胞内部的酸性磷酸酶(ACP)活性被下调(发生在DCs2.4细胞吞噬作用降低时)。最后,我们证明了GL增加了IL-12,IL-10的产生并降低了肿瘤坏死因子α(TNF-α)的产生。这些数据表明GL可以促进DC的成熟,并且这种佐剂样活性可能具有潜在的治疗价值。因此得出的结论是,GL可以在鼠DC上发挥正调控作用。

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