The First Affiliated Hospital, Biomedical Translational Research Institute and School of Pharmacy , Jinan University , Guangzhou , Guangdong 510632 , China.
Department of Basic Medical Research , The Sixth Affiliated Hospital of Guangzhou Medical University, Qing Yuan People's Hospital , Qingyuan , Guangdong 511518 , China.
J Agric Food Chem. 2019 Aug 28;67(34):9522-9531. doi: 10.1021/acs.jafc.9b03647. Epub 2019 Aug 16.
The imbalance of T lymphocyte subsets substantially conduces to disturbed intestinal immune system and succeeding colonic tissue damage in inflammatory bowel diseases. It is considered that regulation of phytochemicals on cytokine production potentially provides a broad prospect for the exploitation of immunomodulatory agents. Here, we reported that oral administration of feruloylated oligosaccharides (FOs) effectively alleviated mice colitis disease induced by dextran sulfate sodium (DSS). FOs decreased the percentage of T helper (Th)17 cells and downregulated the production of Th17-specific cytokines. In contrast, FOs increased the percentage of regulatory T (Treg) cells and elevated the production of Treg-specific cytokines in colons of DSS-challenged mice. These results indicated that FOs restored the immunologic equilibrium of Th17 and Treg subsets, hereby ameliorating the deterioration of colitis. Furthermore, FOs diminished the secretion of interleukin (IL)-23 and IL-6 but enhanced the transforming growth factor-β1 (TGF-β1) in dendritic cells in vitro and in vivo, which contributed to the restoration of Th17 and Treg cells immune balance. The mechanistic analysis showed that the regulation of FOs on IL-23 and IL-6 was associated with the nuclear factor-κ-gene binding signaling pathway and TGF-β1 with mitogen-activated protein kinase-activator protein 1 signaling pathway. Taken together, oral administration of FOs exerted potent immunomodulatory effects against mice colitis via restoring the immune balance of Th17 and Treg cells.
T 淋巴细胞亚群失衡会导致肠道免疫系统紊乱,从而继发炎症性肠病结肠组织损伤。人们认为,植物化学物质对细胞因子产生的调节作用为免疫调节剂的开发提供了广阔的前景。在这里,我们报道了口服阿魏酰低聚糖(FOs)可有效缓解葡聚糖硫酸钠(DSS)诱导的小鼠结肠炎。FOs 降低了 Th17 细胞的百分比,并下调了 Th17 特异性细胞因子的产生。相反,FOs 增加了 DSS 攻击小鼠结肠中调节性 T(Treg)细胞的百分比,并提高了 Treg 特异性细胞因子的产生。这些结果表明,FOs 恢复了 Th17 和 Treg 亚群的免疫平衡,从而改善了结肠炎的恶化。此外,FOs 减少了白细胞介素(IL)-23 和 IL-6 的分泌,但增强了树突状细胞中转化生长因子-β1(TGF-β1)的分泌,这有助于恢复 Th17 和 Treg 细胞的免疫平衡。机制分析表明,FOs 对 IL-23 和 IL-6 的调节与核因子-κB 基因结合信号通路有关,而 TGF-β1 与丝裂原活化蛋白激酶激活蛋白 1 信号通路有关。综上所述,口服 FOs 通过恢复 Th17 和 Treg 细胞的免疫平衡,对小鼠结肠炎发挥了强大的免疫调节作用。