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本文引用的文献

1
Identification of erythroferrone as an erythroid regulator of iron metabolism.鉴定红系铁调素为铁代谢的红系调节因子。
Nat Genet. 2014 Jul;46(7):678-84. doi: 10.1038/ng.2996. Epub 2014 Jun 1.
2
Transforming growth factor-β superfamily ligand trap ACE-536 corrects anemia by promoting late-stage erythropoiesis.转化生长因子-β 超家族配体陷阱 ACE-536 通过促进晚期红细胞生成来纠正贫血。
Nat Med. 2014 Apr;20(4):408-14. doi: 10.1038/nm.3512. Epub 2014 Mar 23.
3
An activin receptor IIA ligand trap corrects ineffective erythropoiesis in β-thalassemia.激活素受体 IIA 配体陷阱纠正β-地中海贫血中的无效红细胞生成。
Nat Med. 2014 Apr;20(4):398-407. doi: 10.1038/nm.3468. Epub 2014 Mar 23.
4
Global transcriptome analyses of human and murine terminal erythroid differentiation.人类和鼠类终末红细胞分化的全球转录组分析。
Blood. 2014 May 29;123(22):3466-77. doi: 10.1182/blood-2014-01-548305. Epub 2014 Mar 17.
5
The pathophysiology and pharmacology of hepcidin.铁调素的病理生理学和药理学。
Trends Pharmacol Sci. 2014 Mar;35(3):155-61. doi: 10.1016/j.tips.2014.01.004. Epub 2014 Feb 17.
6
The multiple facets of the TGF-β family cytokine growth/differentiation factor-15/macrophage inhibitory cytokine-1.TGF-β 家族细胞因子生长/分化因子-15/巨噬细胞抑制因子-1 的多方面特性。
Cytokine Growth Factor Rev. 2013 Aug;24(4):373-84. doi: 10.1016/j.cytogfr.2013.05.003. Epub 2013 Jun 18.
7
Serum hepcidin and growth differentiation factor-15 (GDF-15) levels in polycythemia vera and essential thrombocythemia.血清铁调素和生长分化因子-15(GDF-15)在真性红细胞增多症和原发性血小板增多症中的水平。
Eur J Haematol. 2013 Sep;91(3):228-235. doi: 10.1111/ejh.12150. Epub 2013 Jun 28.
8
Transfusion suppresses erythropoiesis and increases hepcidin in adult patients with β-thalassemia major: a longitudinal study.输血抑制成年重型β地中海贫血患者的红细胞生成并增加其铁调素:一项纵向研究。
Blood. 2013 Jul 4;122(1):124-33. doi: 10.1182/blood-2012-12-471441. Epub 2013 May 8.
9
Serum hepcidin levels and muscle iron proteins in humans injected with low- or high-dose erythropoietin.低剂量或高剂量促红细胞生成素注射对人体血清铁调素水平和肌肉铁蛋白的影响。
Eur J Haematol. 2013 Jul;91(1):74-84. doi: 10.1111/ejh.12122. Epub 2013 May 3.
10
Hypoxia-inducible factor regulates hepcidin via erythropoietin-induced erythropoiesis.缺氧诱导因子通过促红细胞生成素诱导的红细胞生成来调节铁调素。
J Clin Invest. 2012 Dec;122(12):4635-44. doi: 10.1172/JCI63924. Epub 2012 Nov 1.

红细胞生成与铁代谢之间的分子联系。

Molecular liaisons between erythropoiesis and iron metabolism.

作者信息

Kautz Leon, Nemeth Elizabeta

机构信息

Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA.

出版信息

Blood. 2014 Jul 24;124(4):479-82. doi: 10.1182/blood-2014-05-516252. Epub 2014 May 29.

DOI:10.1182/blood-2014-05-516252
PMID:24876565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4110655/
Abstract

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.

摘要

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。