首页> 外文期刊>International Journal of Pharmaceutics >Intracellular disposition of polysaccharides in rat liver parenchymal and nonparenchymal cells.
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Intracellular disposition of polysaccharides in rat liver parenchymal and nonparenchymal cells.

机译:大鼠肝实质和非实质细胞中多糖的细胞内处置。

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摘要

Binding and internalization of arabinogalactan, pullulan, dextran, and mannan were examined in rat liver parenchymal and nonparenchymal cells using (125)I or fluorescein isothiocyanate (FITC) labeled polysaccharides. Binding and uptake of arabinogalactan and pullulan into parenchymal cells was inhibited by asialofetuin, indicating that the asialoglycoprotein receptor is involved in the intracellular disposition of arabinogalactan and pullulan. Uptake of (125)I-labeled dextran to parenchymal cells was unchanged upon addition of excess unlabeled dextran, suggesting that dextran uptake occurs via fluid phase endocytosis. Of the polysaccharides tested, mannan showed the strongest specific association with liver nonparenchymal cells. FITC-labeled polysaccharides showed arabinogalactan and pullulan are internalized to liver parenchymal cells, whereas mannan is internalized to nonparenchymal cells. This study demonstrates that intracellular disposition of polysaccharides in the liver occurs via receptor-mediated endocytosis (RME), indicating that RME plays a role in the biodisposition of these polysaccharides as drug carriers.
机译:使用(125)I或异硫氰酸荧光素(FITC)标记的多糖在大鼠肝实质细胞和非实质细胞中检测阿拉伯半乳聚糖,支链淀粉,葡聚糖和甘露聚糖的结合和内在化。脱唾液酸铁蛋白抑制阿拉伯半乳聚糖和支链淀粉结合到实质细胞中,这表明脱唾液酸糖蛋白受体参与了阿拉伯半乳聚糖和支链淀粉的细胞内处置。添加过量未标记的葡聚糖后,(125)I标记的葡聚糖对实质细胞的摄取未发生变化,这表明葡聚糖的摄取是通过液相内吞作用发生的。在测试的多糖中,甘露聚糖表现出与肝非实质细胞的最强特异性结合。 FITC标记的多糖显示阿拉伯半乳聚糖和支链淀粉被内在肝实质细胞内,而甘露聚糖被内在非实质细胞内。这项研究表明,肝脏中多糖的细胞内沉积是通过受体介导的内吞作用(RME)发生的,这表明RME在这些多糖作为药物载体的生物沉积中起着作用。

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