Ferroportin-mediated iron transport: Expression and regulation

被引:285
|
作者
Ward, Diane M. [1 ]
Kaplan, Jerry [1 ]
机构
[1] Univ Utah, Sch Med, Dept Pathol, Salt Lake City, UT 84132 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2012年 / 1823卷 / 09期
关键词
Ceruloplasmin; Ferroportin; Hepcidin; Homeostasis; Internalization; Iron; HEREDITARY HEMOCHROMATOSIS; FPN1; TRANSCRIPTION; POLYCYTHEMIA MICE; GENE-EXPRESSION; MOLECULAR-BASIS; DOWN-REGULATION; KNOCKOUT MICE; CELLULAR IRON; METAL EFFLUX; HEPCIDIN;
D O I
10.1016/j.bbamcr.2012.03.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The distinguishing feature between iron homeostasis in single versus multicellular organisms is the need for multicellular organisms to transfer iron from sites of absorption to sites of utilization and storage. Ferroportin is the only known iron exporter and ferroportin plays an essential role in the export of iron from cells to blood. Ferroportin can be regulated at many different levels including transcriptionally, post-transcriptionally, through mRNA stability and post-translationally, through protein turnover. Additionally, ferroportin may be regulated in both cell-dependent and cell-autonomous fashions. Regulation of ferroportin is critical for iron homeostasis as alterations in ferroportin may result in either iron deficiency or iron overload. This article is part of a Special Issue entitled: Cell Biology of Metals. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1426 / 1433
页数:8
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