Patel H M, Wild A E
Department of Biochemistry, Charing Cross and Westminster Medical School, London, England.
FEBS Lett. 1988 Jul 18;234(2):321-5. doi: 10.1016/0014-5793(88)80108-x.
Drug carriers such as liposomes are not readily transported across cellular barriers that constitute epithelia. However, certain epithelia (rabbit yolk sac endoderm and enterocytes of suckling rat gut proximal small intestine) are well known to transcytose maternal IgG by Fc receptor-mediated endocytic events. We have shown that coating liposomes with appropriate IgG enhances their transport across these epithelia, as measured both by radioactivity indicative of liposomal membrane or entrapped 125I-PVP and [3H]inulin, and by the hypoglycemic effect of entrapped insulin. It is suggested that these transported liposomes follow a pathway of transcytosis in clathrin-coated vesicles, thus escaping lysosomal degradation.
脂质体等药物载体不易穿过构成上皮组织的细胞屏障。然而,某些上皮组织(兔卵黄囊内胚层和乳鼠近端小肠的肠上皮细胞)通过Fc受体介导的内吞作用转胞吞母体IgG是众所周知的。我们已经表明,用适当的IgG包被脂质体可增强其穿过这些上皮组织的能力,这通过指示脂质体膜或包裹的125I-PVP和[3H]菊粉的放射性以及包裹的胰岛素的降血糖作用来衡量。有人认为,这些被转运的脂质体在网格蛋白包被的小泡中遵循转胞吞途径,从而避免了溶酶体的降解。