Key Laboratory of Food Nutrition and Safety, Ministry of Education, School of Food Engineering and Biotechnology, Tianjin University of Science and Technology, Tianjin, 300457, China,
Inflammation. 2014 Feb;37(1):83-93. doi: 10.1007/s10753-013-9714-z.
A novel Pleurotus nebrodensis polysaccharide (PN50G) was purified, characterized, and cultured with RAW264.7 macrophages to evaluate its bidirectional immunostimulating characteristics. PN50G was purified by using Sepharose 4B gel filtration; the molecular weight of PN50G was distributed at 2,000 kDa. The total protein and carbohydrate constituent ratios in PN50G were 2.6 ± 0.9 % and 92.4 ± 6.1 % (w/w), respectively, which suggests that PN50G may be a major proteo-polysaccharide component. The phagocytosis of macrophages was improved significantly, and remarkable changes were observed in the morphology of PN50G-treated cells. Compared with the control group, the productions of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), interleukin-10 (IL-10), and inducible nitric oxide synthase (iNOS) in the macrophages as well as the messenger RNA expressions were strongly induced by PN50G. Pro-/anti-inflammatory (IL-6/IL-10, TNF-α/IL-10, NO/IL-10) cytokine secretion ratios by lipopolysaccharide-stimulated RAW264.7 macrophages were significantly decreased by PN50G treatments in a dose-dependent manner under an excessive immune experimental model. This study suggests that purified PN50G can improve immunity and suppress immune overactivity in LPS-induced macrophages in a preventive manner to coordinate innate immunity and inflammatory responses.
一种新型的栓菌多糖(PN50G)被分离、鉴定,并与 RAW264.7 巨噬细胞共培养,以评估其双向免疫刺激特性。PN50G 通过 Sepharose 4B 凝胶过滤进行纯化;PN50G 的分子量分布在 2000 kDa。PN50G 中的总蛋白和碳水化合物组成比例分别为 2.6±0.9%和 92.4±6.1%(w/w),这表明 PN50G 可能是一种主要的蛋白多糖成分。巨噬细胞的吞噬作用明显提高,PN50G 处理后的细胞形态发生了显著变化。与对照组相比,PN50G 强烈诱导巨噬细胞产生肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、白细胞介素-10(IL-10)和诱导型一氧化氮合酶(iNOS),并显著诱导其信使 RNA 表达。在过量免疫实验模型下,PN50G 以剂量依赖性方式显著降低脂多糖刺激的 RAW264.7 巨噬细胞中促炎/抗炎(IL-6/IL-10、TNF-α/IL-10、NO/IL-10)细胞因子分泌比值。本研究表明,纯化的 PN50G 可以预防 LPS 诱导的巨噬细胞中提高免疫力和抑制免疫过度激活,以协调先天免疫和炎症反应。