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Investigation of effects of farrerol on suppression of murine T lymphocyte activation in vitro and in vivo

机译:法雷洛尔在体内外抑制鼠T淋巴细胞活化的作用研究

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Farrerol, a new type of 2,3-dihydro-flavonoid, has been isolated from the leaves of Rhododendron dauricum L. In the present study, we found that farrerol exerted potent immunosuppressive effects on murine T cells both in vitro and in vivo. In vitro, farrerol markedly suppressed concanavalin A (ConA)-induced lymphocyte proliferation, Th1 and Th2 cytokine production, cluster of differentiation 4-positive (CD4+) T cell populations, and the ratio of CD4+/cluster of differentiation 8-positive (CD8+) T cells. Moreover, farrerol significantly inhibited the T cell-mediated delayed-type hypersensitivity (DTH) reaction in vivo. In addition, we investigated signal transduction mechanisms to determine the effects of farrerol by Western blotting. The data revealed that farrerol could downregulate the activation of the nuclear factor κB (NF-òB) and nuclear factor of activated T cells 2 (NFAT2) signal transduction pathways. These findings suggested that farrerol has potential effects on the regulation of the immune system and could be developed as a practicable immunosuppressive compound.
机译:从一种杜鹃花的叶子中分离出一种新型的2,3-二氢黄酮类化合物Farrerol。在本研究中,我们发现Farrerol在体外和体内均对鼠T细胞发挥了有效的免疫抑制作用。在体外,法雷洛尔显着抑制伴刀豆球蛋白A(ConA)诱导的淋巴细胞增殖,Th1和Th2细胞因子产生,分化为4阳性(CD4 +)的T细胞群的聚集以及CD4 + /分化为8阳性(CD8 +)的簇的比率T细胞。此外,法雷洛尔在体内显着抑制了T细胞介导的迟发型超敏反应(DTH)。此外,我们研究了信号转导机制,以通过蛋白质印迹法确定法瑞罗的作用。数据显示,法雷洛尔可能下调核因子κB(NF-òB)的活化和活化T细胞2(NFAT2)信号转导通路的核因子。这些发现表明,法雷洛尔对免疫系统的调节具有潜在的影响,可以作为一种实用的免疫抑制化合物开发。

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