Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai'an 271018, Shandong, PR China.
Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, PR China.
Int J Biol Macromol. 2019 Apr 1;126:960-968. doi: 10.1016/j.ijbiomac.2018.12.227. Epub 2018 Dec 24.
Alfalfa polysaccharide (APS), a bioactive compound extracted from alfalfa, has been proposed to exhibit potential growth-promoting and immune-enhancing functions. But, little is known about the cellular immunomodulatory and intrinsic molecular mechanisms. Here we extracted the APS, and performed in vitro experiments to characterize the immunomodulatory functions as well as the molecular mechanisms of APS on RAW 264.7 macrophages cells. Chemical analyses showed that APS was mainly composed of fucose, arabinose, galactose, glucose, xylose, mannose, galacturonic acid and glucuronic acid. The results of in vitro assays demonstrated that 50 and 100 μg/mL APS increased the cell viability of RAW 264.7 cells. The secretion and gene expression of NO/iNOS, IL-6 and TNF-α in APS-induced macrophage cell were significantly enhanced. However, APS-induced TNF-α production was decreased by blocking the MAPK or NF-κB signaling pathways, especially for the blockade of p38. Moreover, APS enhanced the phosphorylation of p38, ERK, and JNK, promoted the degradation of IκBα, and increased the nuclear translocation of NF-κB p65 subunit. Therefore, we demonstrated that APS could improve the immune functions of RAW 264.7 macrophages cells by promoting the cell viability and increasing secretion and gene expressions of NO/iNOS, IL-6 and TNF-α through the MAPK and NF-κB signaling pathways.
苜蓿多糖(APS)是从紫花苜蓿中提取的一种生物活性化合物,据报道具有促进生长和增强免疫的功能。然而,其细胞免疫调节和内在分子机制知之甚少。本研究提取 APS,进行体外实验,以表征 APS 对 RAW 264.7 巨噬细胞的免疫调节功能及分子机制。化学分析表明,APS 主要由岩藻糖、阿拉伯糖、半乳糖、葡萄糖、木糖、甘露糖、半乳糖醛酸和葡萄糖醛酸组成。体外实验结果表明,50 和 100μg/mL APS 可提高 RAW 264.7 细胞的活力。APS 诱导的巨噬细胞中 NO/iNOS、IL-6 和 TNF-α 的分泌和基因表达显著增强。然而,通过阻断 MAPK 或 NF-κB 信号通路,尤其是 p38 通路,可降低 APS 诱导的 TNF-α 产生。此外,APS 增强了 p38、ERK 和 JNK 的磷酸化,促进了 IκBα 的降解,并增加了 NF-κB p65 亚基的核易位。因此,我们证明 APS 通过促进细胞活力以及通过 MAPK 和 NF-κB 信号通路增加 NO/iNOS、IL-6 和 TNF-α 的分泌和基因表达来改善 RAW 264.7 巨噬细胞的免疫功能。