Feng Shibin, Ding Hongyan, Liu Leihong, Peng Chenglu, Huang Yingying, Zhong Fuchao, Li Wei, Meng Tingting, Li Jinchun, Wang Xichun, Li Yu, Wu Jinjie
College of Animal Science and Technology, Anhui Agricultural University, Hefei, Anhui 230036, P.R. China.
Exp Ther Med. 2021 Jan;21(1):20. doi: 10.3892/etm.2020.9452. Epub 2020 Nov 5.
The aim of the present study was to investigate the immunoregulatory effects of polysaccharide (APS) on RAW264.7 cells. The production of cytokines by RAW264.7 cells was analyzed using ELISA, while cell viability and optimal concentration of APS were assessed using the Cell Counting Kit-8 assay. In addition, the mRNA levels of IL-6, inducible nitric oxide synthase (iNOS) and TNF-α were determined by reverse transcription-quantitative PCR analysis. The levels of co-stimulatory molecules and cell cycle distribution were assessed by flow cytometry. Electrophoretic mobility shift assay was used to determine the effects of APS on p65 expression. Compared with controls, APS enhanced the production of NO, the gene expression of TNF-α, IL-6 and iNOS and the protein levels of phosphorylated p65, p38, Jun N-terminal kinase and extracellular signal regulated kinase in RAW264.7 cells, whereas these effects of APS were alleviated by pyrrolidine dithiocarbamate. The results of the present study indicated that the immunoregulatory effects of APS are mediated, at least in part, via the activation of the NF-κB p65/MAPK signaling pathway.
本研究旨在探讨多糖(APS)对RAW264.7细胞的免疫调节作用。采用酶联免疫吸附测定法(ELISA)分析RAW264.7细胞产生细胞因子的情况,同时使用细胞计数试剂盒-8(Cell Counting Kit-8)检测法评估细胞活力和APS的最佳浓度。此外,通过逆转录-定量聚合酶链反应分析测定白细胞介素-6(IL-6)、诱导型一氧化氮合酶(iNOS)和肿瘤坏死因子-α(TNF-α)的mRNA水平。采用流式细胞术评估共刺激分子水平和细胞周期分布。使用电泳迁移率变动分析来确定APS对p65表达的影响。与对照组相比,APS增强了RAW264.7细胞中一氧化氮(NO)的产生、TNF-α、IL-6和iNOS的基因表达以及磷酸化p65、p38、c-Jun氨基末端激酶和细胞外信号调节激酶的蛋白水平,而吡咯烷二硫代氨基甲酸盐可减轻APS的这些作用。本研究结果表明,APS的免疫调节作用至少部分是通过激活核因子-κB p65/丝裂原活化蛋白激酶(NF-κB p65/MAPK)信号通路介导的。