Cellular iron homeostasis is maintained by iron and heme transport proteins that work in concert with ferrireductases, ferroxidases, and chaperones to direct the movement of iron into, within, and out of cells. Systemic iron homeostasis is regulated by the liver-derived peptide hormone, hepcidin. The interface between cellular and systemic iron homeostasis is readily observed in the highly dynamic iron handling of four main cell types: duodenal enterocytes, erythrocyte precursors, macrophages, and hepatocytes. This review provides an overview of how these cell types handle iron, highlighting how iron and heme transporters mediate the exchange and distribution of body iron in health and disease.

译文

:铁和血红素转运蛋白与铁还原酶,铁氧化酶和伴侣蛋白协同作用,维持细胞内铁稳态,从而指导铁进入,进入和离开细胞的运动。系统性铁稳态由肝脏衍生的肽激素hepcidin调节。在铁的四种主要细胞类型的高动态铁处理中,很容易观察到细胞与全身铁稳态之间的界面:十二指肠肠上皮细胞,红细胞前体,巨噬细胞和肝细胞。这篇综述概述了这些细胞类型如何处理铁,着重介绍了铁和血红素转运蛋白如何在健康和疾病中介导体内铁的交换和分布。

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