Vitamin B12 transporters.

Q4 Pharmacology, Toxicology and Pharmaceutics
G J Russell-Jones, D H Alpers
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引用次数: 46

Abstract

The uptake of vitamin B12 from the intestine into the circulation is perhaps the most complex uptake mechanism of all the vitamins, involving no less than five separate VB12-binding molecules, receptors and transporters. Each molecule involved in uptake has a separate affinity and specificity for VB12 as well as a separate cell receptor. Thus VB12 is initially bound by haptocorrin in the stomach, then by IF in the small intestine. An IF receptor is then involved in uptake of the IF-VB12 complex by the intestinal epithelial cell, with the subsequent proteolytic release of VB12 and subsequent binding to TcII. The TcII receptor then transports the TcII-VB12 complex across the cell, whence it is released into the circulation. It is surprising, then, that despite its complexity, it has been possible to harness the vitamin VB12 uptake mechanism to enhance the oral uptake of peptides, proteins, and nanoparticles.

维生素B12转运蛋白。
维生素B12从肠道进入循环系统的吸收可能是所有维生素中最复杂的吸收机制,涉及不少于五种不同的维生素B12结合分子、受体和转运体。参与摄取的每个分子对VB12都有单独的亲和力和特异性,也有单独的细胞受体。因此,VB12最初在胃中与触蛋白结合,然后在小肠中与IF结合。IF受体随后参与肠上皮细胞对IF-VB12复合物的摄取,随后VB12的蛋白水解释放,随后与TcII结合。然后,TcII受体将TcII- vb12复合物在细胞中运输,并在细胞中释放到循环中。令人惊讶的是,尽管它很复杂,但利用维生素VB12摄取机制来增强口服肽、蛋白质和纳米颗粒的摄取是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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