吕弯弯, 李科, 冯仕红, 文雨薇, 秦雪梅, 杜昱光, 李震宇. 黄芪多糖APS-Ⅱ在M细胞上的转运吸收机制初探J. 药学学报, 2024, 59(10): 2820-2827. DOI: 10.16438/j.0513-4870.2024-0103
引用本文: 吕弯弯, 李科, 冯仕红, 文雨薇, 秦雪梅, 杜昱光, 李震宇. 黄芪多糖APS-Ⅱ在M细胞上的转运吸收机制初探J. 药学学报, 2024, 59(10): 2820-2827. DOI: 10.16438/j.0513-4870.2024-0103
LÜ Wan-wan, LI Ke, FENG Shi-hong, WEN Yu-wei, QIN Xue-mei, DU Yu-guang, LI Zhen-yu. Preliminary study of the transport and absorption mechanism of Astragalus polysaccharide-Ⅱ on M cellsJ. Acta Pharmaceutica Sinica, 2024, 59(10): 2820-2827. DOI: 10.16438/j.0513-4870.2024-0103
Citation: LÜ Wan-wan, LI Ke, FENG Shi-hong, WEN Yu-wei, QIN Xue-mei, DU Yu-guang, LI Zhen-yu. Preliminary study of the transport and absorption mechanism of Astragalus polysaccharide-Ⅱ on M cellsJ. Acta Pharmaceutica Sinica, 2024, 59(10): 2820-2827. DOI: 10.16438/j.0513-4870.2024-0103

黄芪多糖APS-Ⅱ在M细胞上的转运吸收机制初探

Preliminary study of the transport and absorption mechanism of Astragalus polysaccharide-Ⅱ on M cells

  • 摘要: 通过建立M细胞模型, 探究黄芪多糖APS-Ⅱ在体内的吸收机制。首先将黄芪多糖(Astragalus polysaccharides, APS) 通过超滤法分为2种不同相对分子质量多糖APS-Ⅰ (> 2 000 kDa) 和APS-Ⅱ (10 kDa), 并制备出黄芪多糖APS-Ⅱ (10 kDa), 然后对其进行荧光标记; 同时通过Caco-2细胞和Raji细胞构建M细胞模型, 并对其进行模型验证。采用转运抑制剂对M细胞模型进行处理, 探究黄芪多糖APS-Ⅱ在M细胞上的转运情况。结果显示, 通过结构与活性验证FITC已成功标记到了APS-Ⅱ的末端, 同时M细胞模型构建成功, 并发现APS-Ⅱ可以被M细胞所转运, 通过5-(N-乙基-N-异丙基) 阿米洛利(EIPA)、染料木素(genistein)、dynasore和诺考达唑(nocodazole) 4种转运抑制剂说明APS-Ⅱ可能通过网格蛋白和小窝蛋白介导的内吞作用进入细胞。

     

    Abstract: To explore the absorption mechanism of APS-Ⅱ in vivo by establishing M cell model. First, Astragalus polysaccharides (APS) was divided into two different molecular weight polysaccharides APS-Ⅰ (> 2 000 kDa) and APS-Ⅱ (10 kDa) by ultrafiltration, and APS-Ⅱ (10 kDa) was prepared and fluorescently labeled. Meanwhile, M cell model was constructed by Caco-2 cells and Raji cells. The M cell model was treated with transport inhibitors to explore the transport of APS-Ⅱ on M cells. The results show that FITC has been successfully labeled to the end of APS-Ⅱ, and the M cell model was successfully constructed, which found that APS-Ⅱ could be transported by M cells, and four transport inhibitors of 5-(N-ethyl-N-isopropyl) amiloride (EIPA), genistein, dynasore and nocodazole indicated that APS-Ⅱ may enter cells through clathrin and caveolin-mediated endocytosis.

     

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