Here we investigate the regulation of hepcidin, a hormone that inhibits dietary iron absorption and macrophage iron recycling, by the serum iron-binding protein transferrin. Mice deficient in transferrin (Tfhpx/hpx) and hemojuvelin (Hjv-/-), a gene mutated in juvenile hemochromatosis, a disease of hepcidin deficiency and iron overload, were generated. While Tfhpx/hpx Hjv+/+ and Tfhpx/hpx Hjv-/- phenotypes did not differ markedly, transferrin treatment and RBC transfusions robustly increased hepcidin levels in Tfhpx/hpx Hjv+/+ but not Tfhpx/hpx Hjv-/-mice. These results suggest that, while hemojuvelin is not essential for the establishment or maintenance of hepcidin deficiency in transferrin-deficient mice, hemojuvelin is essential for transferrin-dependent and tansferrin-indepen-dent hepcidin expression in conditions of iron overload. © 2012 Ferrata Storti Foundation.
CITATION STYLE
Bartnikas, T. B., & Fleming, M. D. (2012). Hemojuvelin is essential for transferrin-dependent and transferrin-independent hepcidin expression in mice. Haematologica, 97(2), 189–192. https://doi.org/10.3324/haematol.2011.054031
Mendeley helps you to discover research relevant for your work.