Kautz Leon, Nemeth Elizabeta
Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA.
Blood. 2014 Jul 24;124(4):479-82. doi: 10.1182/blood-2014-05-516252. Epub 2014 May 29.
Although most circulating iron in blood plasma is destined for erythropoiesis, the mechanisms by which erythropoietic demand modulates the iron supply ("erythroid regulators") remain largely unknown. Iron absorption, plasma iron concentrations, and tissue iron distribution are tightly controlled by the liver-produced hormone hepcidin. During the last decade, much progress has been made in elucidating hepcidin regulation by iron and inflammation. This review discusses the less understood mechanisms and mediators of hepcidin suppression in physiologically and pathologically stimulated erythropoiesis.
虽然血浆中大多数循环铁都用于红细胞生成,但红细胞生成需求调节铁供应的机制(“红细胞生成调节因子”)在很大程度上仍不清楚。铁的吸收、血浆铁浓度和组织铁分布受肝脏产生的激素铁调素严格控制。在过去十年中,在阐明铁和炎症对铁调素的调节方面取得了很大进展。本综述讨论了在生理和病理刺激的红细胞生成中铁调素抑制的较少为人所知的机制和介质。