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Iron imports. II. Iron uptake at the apical membrane in the intestine

Authors :
Mackenzie, Bryan
Garrick, Michael D.
Source :
The American Journal of Physiology. Dec, 2005, Vol. 289 Issue 6, pG981, 6 p.
Publication Year :
2005

Abstract

How does iron enter enterocytes? Ablating SLC11A2, the gene for the divalent metal ion transporter DMT1, supports evidence from the Belgrade rat and mk mouse models establishing DMT1 as the primary mechanism serving apical uptake of nonheme iron. DMT1 harnesses the energy from the proton electrochemical potential gradient to drive active transport of [Fe.sup.2+] (and perhaps [Mn.sup.2+] and other metal ions) into enterocytes. Fe(III) must first be reduced by ascorbic acid and surface ferrireductases. Among these is duodenal cytochrome B (DcytB), but lack of an obvious phenotype in DcytB (Cybrd1) knockout mice suggests ferrireductase redundancy. Our understanding of heine absorption has lagged, but the time is ripe for gains. anemia: duodenal cytochrome B; divalent metal ion transporter; ferroportin; hemochromatosis; iron absorption; Nramp2; SLC11A2

Details

Language :
English
ISSN :
00029513
Volume :
289
Issue :
6
Database :
Gale General OneFile
Journal :
The American Journal of Physiology
Publication Type :
Academic Journal
Accession number :
edsgcl.140997245