Gao Hui-Ling, Lei Lin-Sheng, Yu Chuan-Lin, Zhu Zheng-Guang, Chen Na-Na, Wu Shu-Guang
Institute of Pharmaceutical Sciences, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2009 Mar;29(3):458-61.
To investigate the immunomodulatory effects of Fomes fomentarius polysaccharides (FFP) in mice.
MTT assay was employed to evaluate the in vitro metabolic activity of the mouse splenocytes treated with FFP at different concentrations, and the secretion of tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (INF-gamma) and interleukin 2 (IL-2) from the cells were measured by enzyme-linked immunosorbent assay. The changes in the phagocytotic activity of mouse macrophage in response to FFP treatment were evaluated by phagocytosis percentage of chicken red blood cells (CRBCs). The effect of FFP on the humoral immunity was assessed in mice immunized with sheep red blood cells (SRBCs) by measuring the serum levels of specific antibody (hemolysin) against SRBCs.
FFP at the concentrations of 25, 50, and 100 microg/ml all significantly enhanced the metabolic activity of mouse splenocytes in vitro and increased the production of TNF-alpha, IFN-gamma and IL-2. FFP treatment also markedly enhanced the metabolic activity of mouse peritoneal exudate cells and TNF-alpha production by the cells. At the doses of 25, 50, and 100 mg/kg, FFP significantly increased serum hemolysin level in mice immunized with SRBCs, and FFP at 50 and 100 mg/kg obviously increased the capacity of mouse peritoneal macrophages in vivo for CRBC phagocytosis.
FFP can promote the secretion of TNF-alpha, IFN-gamma and IL-2 by mouse immunocytes and enhance mouse humoral immune response and the phagocytotic activity of the macrophages.
研究云芝多糖(FFP)对小鼠的免疫调节作用。
采用MTT法评估不同浓度FFP处理的小鼠脾细胞的体外代谢活性,并用酶联免疫吸附测定法检测细胞中肿瘤坏死因子-α(TNF-α)、干扰素-γ(INF-γ)和白细胞介素2(IL-2)的分泌。通过鸡红细胞(CRBC)吞噬百分比评估FFP处理对小鼠巨噬细胞吞噬活性的影响。通过测量针对绵羊红细胞(SRBC)的特异性抗体(溶血素)的血清水平,评估FFP对用SRBC免疫的小鼠体液免疫的影响。
浓度为25、50和100μg/ml的FFP均显著增强小鼠脾细胞的体外代谢活性,并增加TNF-α、IFN-γ和IL-2的产生。FFP处理还显著增强小鼠腹腔渗出细胞的代谢活性和细胞产生的TNF-α。在25、50和100mg/kg的剂量下,FFP显著提高用SRBC免疫的小鼠的血清溶血素水平,50和100mg/kg的FFP明显提高小鼠腹腔巨噬细胞在体内对CRBC的吞噬能力。
FFP可促进小鼠免疫细胞分泌TNF-α、IFN-γ和IL-2,增强小鼠体液免疫反应和巨噬细胞的吞噬活性。