Skip to main navigation Skip to search Skip to main content

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

  • University of Cincinnati

Research output: Contribution to journalReview articlepeer-review

191 Scopus citations

Abstract

How does iron enter enterocytes? Ablating SLC11A2, the gene for the divalent metal ion transporter DMT1, supports evidence from the Belgrade rat and ink 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 Fe2+ (and perhaps Mn2+ 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 heme absorption has lagged, but the time is ripe for gains.

Original languageEnglish
Pages (from-to)G981-G986
JournalAmerican Journal of Physiology - Gastrointestinal and Liver Physiology
Volume289
Issue number6 52-6
DOIs
StatePublished - Dec 2005

Keywords

  • Anemia
  • Divalent metal ion transporter
  • Duodenal cytochrome B
  • Ferroportin
  • Hemochromatosis
  • Iron absorption
  • Nramp2
  • SLC11A2

Fingerprint

Dive into the research topics of 'Iron Imports. II. Iron uptake at the apical membrane in the intestine'. Together they form a unique fingerprint.

Cite this