Recently, mutations causing juvenile hemochromatosis have been identified in a novel gene, hemojuvelin (HJV), located on chromosome 1. Mouse models of this disease have now been developed by 2 groups, Huang et al. and Niederkofler et al., through targeted disruption of the Hjv gene (see the related articles beginning on pages 2180 and 2187). These mutant mice will allow further investigation into the role of HJV in the regulation of iron homeostasis, a role that to date remains elusive.
Sophie Vaulont, Dan-Qing Lou, Lydie Viatte, Axel Kahn
Title and authors | Publication | Year |
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Cross-talk between the mitogen activated protein kinase and bone morphogenetic protein/hemojuvelin pathways is required for the induction of hepcidin by holotransferrin in primary mouse hepatocytes
G Ramey, JC Deschemin, S Vaulont |
Haematologica | 2009 |
Kupffer cells modulate iron homeostasis in mice via regulation of hepcidin expression
M Theurl, I Theurl, K Hochegger, P Obrist, N Subramaniam, N van Rooijen, K Schuemann, G Weiss |
Journal of Molecular Medicine | 2008 |
Hepcidin expression in mouse retina and its regulation via lipopolysaccharide/Toll-like receptor-4 pathway independent of Hfe
JP Gnana-Prakasam, PM Martin, BA Mysona, P Roon, SB Smith, V Ganapathy |
Biochemical Journal | 2008 |