Abstract
Iron is an essential trace nutrient, but its oxidized forms in the Earth’s crust are poorly bioaccessible. Humans and other mammals strictly conserve and recycle iron, so their iron content is determined by the rate of absorption of available iron from their diet. In humans and other mammals, most of the iron is in hemoglobin of erythrocytes. The liver functions as the main iron storage organ. Iron absorption, storage, and tissue distribution are subject to complex hormonal regulation by the iron hormone hepcidin. Hepcidin together with its receptor, the cellular iron exporter ferroportin, controls the major fluxes of iron into blood plasma: intestinal iron absorption, the delivery of recycled iron from macrophages, and the release of stored iron from hepatocytes. Hepcidin is feedback-regulated by plasma iron concentration and iron stores. Erythrocyte precursors in the marrow are the dominant consumers of iron, and they modulate their iron supply by secreting the hepcidin-suppressive hormone erythroferrone. Hepcidin and ferroportin also play a role in host defense and inflammation, and hepcidin synthesis is induced by inflammatory signals, mainly IL-6. Environmental and genetic effects commonly result in disorders of iron homeostasis including iron deficiency anemia, anemia of inflammation, and iron overload toxicity.
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Ganz, T. (2022). Iron Biology: Metabolism and Homeostasis. In: Karakochuk, C.D., Zimmermann, M.B., Moretti, D., Kraemer, K. (eds) Nutritional Anemia. Nutrition and Health. Springer, Cham. https://doi.org/10.1007/978-3-031-14521-6_2
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