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Forkhead-box transcription factor 1 affects the apoptosis of natural regulatory T cells by controlling Aven expression

机译:叉头箱转录因子1通过控制Aven表达影响自然调节性T细胞的凋亡

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Background Regulatory T (Treg) cells play important roles in autoimmune diseases, cancer, and organ transplantation. Forkhead box protein o1 (Foxo1) and IL-7Rα(CD127) are closely related to the homeostasis of Treg cells. However, the mechanism underlying Treg proliferation and activation remains unclear. Here, we evaluated how the over-expression of Foxo1 affects Treg cell proliferation via intracellular signaling. nTreg cells were transfected separately with Foxo1 and Aven small-interfering RNA (siRNA) or over-expression plasmid. The expression of signaling pathway genes and CD127 was confirmed using RT-qPCR and western blot analysis. The expression of cell surface molecules and apoptosis was confirmed by Flow Cytometry 3-(4, 5-Dimethylthiazol-2-yl) 2,5- diphenyltetrazolium bromide for cell proliferation assays. Results Foxo1 strengthened the proliferative ability of Treg cells by activating IL-7/CD127 signaling. In addition, Foxo1 suppressed Treg cell apoptosis by regulating Aven expression. Conclusions The results in this study indicated that Foxo1 is a positive regulatory factor for the proliferation and activity of Treg cells. Foxo1 might be a potential target for the activation of nTreg cells in vivo and in vitro.
机译:背景调节性T(Treg)细胞在自身免疫性疾病,癌症和器官移植中起重要作用。叉头盒蛋白o1(Foxo1)和IL-7Rα(CD127)与Treg细胞的体内稳态密切相关。但是,Treg增殖和激活的机制尚不清楚。在这里,我们评估了Foxo1的过表达如何通过细胞内信号传导影响Treg细胞增殖。用Foxo1和Aven小干扰RNA(siRNA)或过表达质粒分别转染nTreg细胞。 RT-qPCR和Western blot分析证实了信号通路基因和CD127的表达。细胞表面分子的表达和凋亡通过流式细胞术3-(4,5-Dimethylthiazol-2-yl)2,5-diphenyltetrazolium bromide进行了细胞增殖测定。结果Foxo1通过激活IL-7 / CD127信号传导增强Treg细胞的增殖能力。此外,Foxo1通过调节Aven表达抑制Treg细胞凋亡。结论这项研究的结果表明Foxo1是Treg细胞增殖和活性的积极调节因子。 Foxo1可能是体内和体外激活nTreg细胞的潜在靶标。

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