4.5 Review Book Chapter

Iron-Sensing Proteins that Regulate Hepcidin and Enteric Iron Absorption

Journal

ANNUAL REVIEW OF NUTRITION, VOL 30
Volume 30, Issue -, Pages 149-171

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev.nutr.012809.104801

Keywords

hemochromatosis; bone morphogenetic protein; transferrin receptor; matriptase-2; hypoxia-inducible factor

Funding

  1. NIDDK NIH HHS [DK 080706] Funding Source: Medline
  2. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK080706] Funding Source: NIH RePORTER

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The human body cannot actively excrete excess iron. As a consequence, iron absorption must be strictly regulated to ensure adequate iron uptake and prevent toxic iron accumulation. Iron absorption is controlled chiefly by hepcidin, the iron-regulatory hormone. Produced by the liver and secreted into the circulation, hepcidin regulates iron metabolism by inhibiting iron release from cells, including duodenal enterocytes, which mediate the absorption of dietary iron. Hepcidin production increases in response to iron loading and decreases in iron deficiency. Such regulation of hepcidin expression serves to modulate iron absorption to meet body iron demand. This review discusses the proteins that orchestrate hepatic hepcidin production and iron absorption by the intestine. Emphasis is placed on the proteins that directly sense iron and how they coordinate and tine-tune the molecular, cellular, and physiologic responses to iron deficiency and overload.

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