A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation

被引:1131
作者
McKie, AT
Marciani, P
Rolfs, A
Brennan, K
Wehr, K
Barrow, D
Miret, S
Bomford, A
Peters, TJ
Farzaneh, F
Hediger, MA
Hentze, MW
Simpson, RJ
机构
[1] Univ London Kings Coll, Guys Kings & St Thomas Sch Med, Dept Mol Med, London SE5, England
[2] Univ London Kings Coll, Guys Kings & St Thomas Sch Med, Dept Clin Biochem, London SE5, England
[3] Univ London Kings Coll, Guys Kings & St Thomas Sch Med, Inst Liver Studies, London SE5, England
[4] European Mol Biol Lab, Gene Express Programme, D-69117 Heidelberg, Germany
[5] Brigham & Womens Hosp, Membrane Biol Program, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, Div Renal, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Inst Med, Boston, MA 02115 USA
[8] Univ Barcelona, Fac Biol, Dept Fisiol, E-08028 Barcelona, Spain
基金
美国国家卫生研究院; 英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1016/S1097-2765(00)80425-6
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
Iron absorption by the duodenal mucosa is initiated by uptake of ferrous Fe(ll) iron across the brush border membrane and culminates in transfer of the metal across the basolateral membrane to the portal vein circulation by an unknown mechanism. We describe here the isolation and characterization of a novel cDNA (Ireg1) encoding a duodenal protein that is localized to the basolateral membrane of polarized epithelial cells. Ireg1 mRNA and protein expression are increased under conditions of increased iron absorption, and the 5' UTR of the Ireg1 mRNA contains a functional iron-responsive element (IRE). IREG1 stimulates iron efflux following expression in Xenopus oocytes. We conclude that IREG1 represents the long-sought duodenal iron export protein and is upregulated in the iron overload disease, hereditary hemochromatosis.
引用
收藏
页码:299 / 309
页数:11
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