Hemojuvelin is essential for dietary iron sensing, and its mutation leads to severe iron overload.

Abstract

Iron homeostasis plays a critical role in many physiological processes, notably synthesis of heme proteins. Dietary iron sensing and inflammation converge in the control of iron absorption and retention by regulating the expression of hepcidin, a regulator of the iron exporter ferroportin. Human mutations in the glycosylphosphatidylinositol-anchored protein hemojuvelin (HJV; also known as RGMc and HFE2) cause juvenile hemochromatosis, a severe iron overload disease, but the way in which HJV intersects with the iron regulatory network has been unclear. Here we show that, within the liver, mouse Hjv is selectively expressed by periportal hepatocytes and also that Hjv-mutant mice exhibit iron overload as well as a dramatic decrease in hepcidin expression. Our findings define a key role for Hjv in dietary iron sensing and also reveal that cytokine-induced inflammation regulates hepcidin expression through an Hjv-independent pathway.

• Authors: Vera Niederkofler, Rishard Salie, Silvia Arber
• Journal: The Journal of clinical investigation (J Clin Invest) Vol. 115 Issue 8 Pg. 2180-6 (Aug 2005) ISSN: 0021-9738 [Print] United States
• PMID: 16075058 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Cytokines
• GPI-Linked Proteins
• HJV protein, mouse
• Hemochromatosis Protein
• Iron, Dietary
• Membrane Proteins

Topics

• Animals
• Cytokines (metabolism)
• GPI-Linked Proteins
• Gene Expression Regulation
• Hemochromatosis (genetics, metabolism, pathology)
• Hemochromatosis Protein
• Hepatocytes (metabolism, pathology)
• Humans
• Inflammation (genetics, metabolism)
• Iron Overload (genetics, metabolism)
• Iron, Dietary (metabolism)
• Membrane Proteins (genetics, metabolism)
• Mice
• Mice, Mutant Strains
• Signal Transduction (genetics)