Deregulation of proteins involved in iron metabolism in hepcidin-deficient mice

Blood. 2005 Jun 15;105(12):4861-4. doi: 10.1182/blood-2004-12-4608. Epub 2005 Feb 15.

Abstract

Evidence is accumulating that hepcidin, a liver regulatory peptide, could be the common pathogenetic denominator of all forms of iron overload syndromes including HFE-related hemochromatosis, the most prevalent genetic disorder characterized by inappropriate iron absorption. To understand the mechanisms whereby hepcidin controls iron homeostasis in vivo, we have analyzed the level of iron-related proteins by Western blot and immunohistochemistry in hepcidin-deficient mice, a mouse model of severe hemochromatosis. These mice showed important increased levels of duodenal cytochrome b (Dcytb), divalent metal transporter 1 (DMT1), and ferroportin compared with control mice. Interestingly, the level of ferroportin was coordinately up-regulated in the duodenum, the spleen, and the liver (predominantly in the Kupffer cells). Finally, we also evidenced a decrease of ceruloplasmin in the liver of hepcidin-deficient mice. We hypothesized that the deregulation of these proteins might be central in the pathogenesis of iron overload, providing key therapeutic targets for iron disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / genetics*
  • Antimicrobial Cationic Peptides / physiology*
  • Blotting, Western
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism
  • Cytochromes b / genetics
  • Cytochromes b / metabolism
  • Disease Models, Animal
  • Duodenum / metabolism
  • Gene Expression Regulation*
  • Hemochromatosis
  • Hepcidins
  • Immunohistochemistry
  • Iron / metabolism*
  • Iron-Binding Proteins / genetics
  • Liver / metabolism
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Spleen / metabolism
  • Transgenes
  • Up-Regulation

Substances

  • Antimicrobial Cationic Peptides
  • Cation Transport Proteins
  • Hamp protein, mouse
  • Hepcidins
  • Iron-Binding Proteins
  • metal transporting protein 1
  • solute carrier family 11- (proton-coupled divalent metal ion transporters), member 2
  • Cytochromes b
  • Iron