Tsinghua University, Beijing, China.
IUBMB Life. 2010 Mar;62(3):176-82. doi: 10.1002/iub.291.
Studies on dietary zinc absorption are of fundamental nutritional significance, owing to the ubiquity of zinc in biological processes and the severe outcomes of zinc deficiency in humans. Insights into the molecular basis of dietary zinc absorption have advanced in recent years through functional characterization of zinc transporters in cell culture, immunohistochemical studies on rodent intestine and analysis of gene knockout mice. Zinc transporters with manifested expression in enterocytes include ZnT1, ZnT2, ZnT4, ZnT5, ZnT6, ZnT7, Zip4, and Zip5. Among them, ZIP4, the gene responsible for Acrodermatitis enteropathica, an inherited human zinc deficiency, mediates dietary zinc uptake into enterocytes across the apical membrane, while ZnT1 is involved in zinc efflux from enterocytes across the basolateral membrane into circulation. The intracellular trafficking pathways for zinc retention and movement between apical and basolateral sides of the enterocytes have yet to be defined. The utilization of Drosophila model in elucidating molecular mechanisms of dietary zinc absorption is also discussed in this review.
饮食锌吸收的研究具有重要的营养意义,因为锌在生物过程中普遍存在,而人类缺锌会导致严重后果。近年来,通过细胞培养中锌转运体的功能特征、对啮齿动物肠道的免疫组织化学研究以及基因敲除小鼠的分析,人们对饮食锌吸收的分子基础有了更深入的了解。在肠细胞中表达的锌转运体包括 ZnT1、ZnT2、ZnT4、ZnT5、ZnT6、ZnT7、Zip4 和 Zip5。其中,负责先天性人类缺锌症——肠病性肢端皮炎的基因 ZIP4 介导了膳食锌通过肠细胞的顶膜进入细胞,而 ZnT1 则参与了锌从肠细胞的基底外侧膜向循环系统的外排。锌在肠细胞顶侧和基底外侧之间的保留和移动的细胞内运输途径尚未确定。本文还讨论了利用果蝇模型阐明饮食锌吸收的分子机制。