Expression of the DMT1 (NRAMP2/DCT1) iron transporter in mice with genetic iron overload disorders.


Journal Article

Iron overload is highly prevalent, but its molecular pathogenesis is poorly understood. Recently, DMT1 was shown to be a major apical iron transporter in absorptive cells of the duodenum. In vivo, it is the only transporter known to be important for the uptake of dietary non-heme iron from the gut lumen. The expression and subcellular localization of DMT1 protein in 3 mouse models of iron overload were examined: hypotransferrinemic (Trf(hpx)) mice, Hfe knockout mice, and B2m knockout mice. Interestingly, in Trf(hpx) homozygotes, DMT1 expression was strongly induced in the villus brush border when compared to control animals. This suggests that DMT1 expression is increased in response to iron deficiency in the erythron, even in the setting of systemic iron overload. In contrast, no increase was seen in DMT1 expression in animals with iron overload resembling human hemochromatosis. Therefore, it does not appear that changes in DMT1 levels are primarily responsible for iron loading in hemochromatosis.

Full Text

Duke Authors

Cited Authors

  • Canonne-Hergaux, F; Levy, JE; Fleming, MD; Montross, LK; Andrews, NC; Gros, P

Published Date

  • February 15, 2001

Published In

Volume / Issue

  • 97 / 4

Start / End Page

  • 1138 - 1140

PubMed ID

  • 11159549

Pubmed Central ID

  • 11159549

International Standard Serial Number (ISSN)

  • 0006-4971

Digital Object Identifier (DOI)

  • 10.1182/blood.v97.4.1138


  • eng

Conference Location

  • United States