Monobe Manami, Ema Kaori, Kato Fumiko, Hirokane Hisako, Maeda-Yamamoto Mari
National Institute of Vegetable and Tea Science, 2769 Kanaya, Shimada, Shizuoka 428-8501, Japan.
J Agric Food Chem. 2007 Apr 4;55(7):2543-7. doi: 10.1021/jf063426r. Epub 2007 Mar 6.
A technique for screening immune-enhancing polysaccharides in food using the phagocytotic activity of 1,25-dihydroxyvitamin D3 (VD3)-differentiated HL60 cells is presented. HL60 cells, a human acute promyelocytic cell line, can differentiate along the monocytic lineage following exposure to VD3 or phorbol-12-myristate-13-acetate (PMA). For differentiated cells along the monocytic pathway, HL60 cells were maintained in RPMI 1640 medium supplemented with 10% FBS and 120 nM VD3 for more than 1 week. VD3-differentiated HL60 cells were seeded into 48-well plates, YG-labeled microspheres and polysaccharides were added and mixed using a plate shaker at 1100 rpm for 30 s, and then the mixture was incubated overnight at 37 degrees C in 5% CO2. The cells were fixed with 2% formaldehyde and resuspended in phosphate-buffered saline. The rate of phagocytosis was measured with a flow cytometer. VD3-differentiated cells but not non- and PMA-differentiated cells resulted in an elevation of phagocytic activity by various immune-enhancing polysaccharides in foods.
本文介绍了一种利用1,25 - 二羟基维生素D3(VD3)分化的HL60细胞的吞噬活性来筛选食品中免疫增强多糖的技术。HL60细胞是一种人急性早幼粒细胞系,在暴露于VD3或佛波醇-12-肉豆蔻酸酯-13-乙酸酯(PMA)后可沿单核细胞谱系分化。对于沿单核细胞途径分化的细胞,将HL60细胞在补充有10%胎牛血清和120 nM VD3的RPMI 1640培养基中培养超过1周。将VD3分化的HL60细胞接种到48孔板中,加入YG标记的微球和多糖,使用平板振荡器以1100 rpm振荡30秒使其混合,然后将混合物在37℃、5% CO2条件下孵育过夜。用2%甲醛固定细胞并重悬于磷酸盐缓冲盐水中。用流式细胞仪测量吞噬率。VD3分化的细胞而非未分化和PMA分化的细胞,会因食品中各种免疫增强多糖而导致吞噬活性升高。