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Human iron transporters

Research output: Contribution to journalReview articlepeer-review

49 Scopus citations

Abstract

Human iron transporters manage iron carefully because tissues need iron for critical functions, but too much iron increases the risk of reactive oxygen species. Iron acquisition occurs in the duodenum via divalent metal transporter (DMT1) and ferroportin. Iron trafficking depends largely on the transferrin cycle. Nevertheless, non-digestive tissues have a variety of other iron transporters that may render DMT1 modestly redundant, and DMT1 levels exceed those needed for the just-mentioned tasks. This review begins to consider why and also describes advances after 2008 that begin to address this challenge.

Original languageEnglish
Pages (from-to)45-54
Number of pages10
JournalGenes and Nutrition
Volume6
Issue number1
DOIs
StatePublished - Feb 2011

Keywords

  • Divalent metal transporter (DMT1)
  • Ferric reductase
  • Ferroportin
  • Iron regulatory protein (IRP)
  • Iron-responsive element (IRE)
  • Isoforms
  • Transferrin

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