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铁调素的生物学特性及其治疗应用。

Hepcidin biology and therapeutic applications.

机构信息

David Geffen School of Medicine, UCLA, 10833 LeConte Ave, CHS 37-131, Los Angeles, CA 90095, USA.

出版信息

Expert Rev Hematol. 2010 Apr;3(2):153-5. doi: 10.1586/ehm.10.1.

Abstract

The hepatic peptide hormone hepcidin regulates plasma iron concentrations and tissue iron distribution by inhibiting dietary iron absorption and mobilization of iron from stores in macrophages and hepatocytes. Dysregulation of hepcidin production underlies many iron disorders. Deficient production of hepcidin causes systemic iron overload in hereditary hemochromatosis and iron-loading anemias, such as β-thalassemia, whereas hepcidin excess contributes to the development of anemia in inflammatory disorders and chronic kidney disease, and may cause erythropoietin resistance. The Scientific Program on Iron and Heme session at the 51st ASH annual meeting discussed recent advances in understanding hepcidin biology and explored the potential for hepcidin therapeutic applications. The session included three 30-min presentations.

摘要

肝肽激素铁调素通过抑制膳食铁吸收和巨噬细胞及肝细胞中铁库的动员来调节血浆铁浓度和组织铁分布。铁调素生成失调是许多铁代谢紊乱的基础。铁调素生成不足导致遗传性血色素沉着症和铁负荷性贫血(如β-地中海贫血)的全身性铁过载,而铁调素生成过多则导致炎症性疾病和慢性肾脏病贫血的发生,并可能导致红细胞生成素抵抗。第 51 届美国血液学会年会的铁和血红素科学计划会议讨论了铁调素生物学理解方面的最新进展,并探讨了铁调素治疗应用的潜力。会议包括三个 30 分钟的演讲。

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