Identification of an intestinal heme transporter

被引:526
作者
Shayeghi, M
Latunde-Dada, GO
Oakhill, JS
Laftah, AH
Takeuchi, K
Halliday, N
Khan, Y
Warley, A
McCann, FE
Hider, RC
Frazer, DM
Anderson, GJ
Vulpe, CD
Simpson, RJ
McKie, AT
机构
[1] Kings Coll London, Dept Life Sci, Nutr Sci Res Div, London SE1 9NN, England
[2] St Thomas Hosp, Rayne Inst, GKT Dept Ophthalmol, London SE1 7EH, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Sci Biol, London SW7 2AZ, England
[4] Kings Coll London, Dept Pharm, London SE1 9NN, England
[5] Queensland Inst Med Res, Iron Metab Lab, Brisbane, Qld, Australia
[6] Univ Calif Berkeley, Dept Nutr Sci & Toxicol, Berkeley, CA 94720 USA
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1016/j.cell.2005.06.025
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
Dietary heme iron is an important nutritional source of iron in carnivores and omnivores that is more readily absorbed than non-heme iron derived from vegetables and grain. Most heme is absorbed in the proximal intestine, with absorptive capacity decreasing distally. We utilized a subtractive hybridization approach to isolate a heme transporter from duodenum by taking advantage of the intestinal gradient for heme absorption. Here we show a membrane protein named HCP1 (heme carrier protein 1), with homology to bacterial metal-tetracycIine transporters, mediates heme uptake by cells in a temperature-dependent and saturable manner. HCP1 mRNA was highly expressed in duodenum and regulated by hypoxia. HCP1 protein was iron regulated and localized to the brush-border membrane of duodenal enterocytes in iron deficiency.
引用
收藏
页码:789 / 801
页数:13
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