Genomics Research Center, Academia Sinica, No. 128, Academia Road, Sec. 2, Nankang, Taipei 115, Taiwan.
Bioorg Med Chem. 2010 Dec 15;18(24):8583-91. doi: 10.1016/j.bmc.2010.10.016. Epub 2010 Nov 4.
The polysaccharide fraction of Ganoderma lucidum (F3) was found to benefit our health in many ways by influencing the activity of tissue stem/progenitor cells. In this study, F3 was found to promote the adipose tissue MSCs' aggregation and chondrosphere formation, with the increase of CAM (N-CAM, I-CAM) expressions and autokine (BMP-2, IL-11, and aggrecan) secretions, in an in vitro chondrogenesis assay. In a stem cell expansion culture, it possesses the thrombopoietin (TPO) and GM-CSF like functions to enhance the survival/renewal abilities of primitive hematopoietic stem/progenitor cells (HSCs). F3 was found to promote the dendrite growth of blood mononuclear cells (MNCs) and the expression of cell adhesion molecules in the formation of immature dendritic cells (DC). On the other hand, F3 exhibited inhibitory effects on blood endothelial progenitor (EPC) colony formation, with concomitant reduction of cell surface endoglin (CD105) and vascular endothelial growth factor receptor-3 (VEGFR-3) marker expressions, in the presence of angiogenic factors. A further cytokine array analysis revealed that F3 indeed inhibited the angiogenin synthesis and enhanced IL-1, MCP-1, MIP-1, RANTES, and GRO productions in the blood EPC derivation culture. Collectively, we have demonstrated that the polysaccharide fraction of G. lucidum F3 exhibits cytokine and chemokine like functions which are beneficial to human tissue stem/progenitor cells by modulating their CAM expressions and biological activities. These findings provide us a better the observation that F3 glycopolysaccharides indeed possesses anti-angiogenic and immune-modulating functions and promotes hematopoietic stem/progenitor cell homing for better human tissue protection, reducing disease progression and health.
灵芝多糖(F3)被发现通过影响组织干细胞/祖细胞的活性,在许多方面有益于我们的健康。在这项研究中,F3 被发现促进脂肪组织间充质干细胞的聚集和软骨球形成,伴随着细胞黏附分子(N-CAM、I-CAM)表达和自分泌因子(BMP-2、IL-11 和聚集蛋白聚糖)的增加,在体外软骨发生试验中。在干细胞扩增培养中,它具有血小板生成素(TPO)和 GM-CSF 样功能,增强原始造血干细胞/祖细胞(HSCs)的存活/更新能力。F3 被发现促进单核细胞(MNC)树突的生长和未成熟树突状细胞(DC)形成中的细胞黏附分子的表达。另一方面,F3 表现出对血液内皮祖细胞(EPC)集落形成的抑制作用,同时伴随着细胞表面内胚层蛋白(CD105)和血管内皮生长因子受体-3(VEGFR-3)标志物表达的减少,在存在血管生成因子的情况下。进一步的细胞因子阵列分析表明,F3 确实抑制了血管生成素的合成,并增强了血液 EPC 来源培养物中白细胞介素-1、单核细胞趋化蛋白-1、巨噬细胞炎性蛋白-1、调节激活正常 T 细胞表达和分泌因子和趋化因子配体-5 的产生。总之,我们已经证明灵芝多糖 F3 具有细胞因子和趋化因子样功能,通过调节它们的细胞黏附分子表达和生物活性,有益于人体组织干细胞/祖细胞。这些发现为我们提供了更好的观察结果,即 F3 糖蛋白确实具有抗血管生成和免疫调节功能,并促进造血干细胞/祖细胞归巢,以更好地保护人体组织,减少疾病进展和健康风险。