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Blood, 15 December 2004, Vol. 104, No. 13, pp. 4308-4310.
Prepublished online as a Blood First Edition Paper on August 17, 2004; DOI 10.1182/blood-2004-06-2422.
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Submitted June 28, 2004
Accepted August 1, 2004
Expression of Rgmc, the murine ortholog of hemojuvelin gene, is modulated by development and inflammation, but not by iron status or erythropoietin
Jan Krijt*, Martin Vokurka, Ko-Tung Chang, and Emanuel Necas
Institute of Pathological Physiology, First Faculty of Medicine, Charles University, Prague, Czech Republic
* Corresponding author; email: jkri{at}lf1.cuni.cz.
Mutations of hepcidin (HAMP) and hemojuvelin (HJV) genes have been recently demonstrated to result in juvenile hemochromatosis. Expression of HAMP is regulated by iron status or infection, whereas regulation of HJV is yet unknown. Using quantitative real-time PCR, we compared expression of Hamp and Rgmc (the murine ortholog of HJV) in livers of mice treated with iron, erythropoietin or lipopolysaccharide, as well as during fetal and postnatal development. Iron overload increased Hamp expression without effect on Rgmc mRNA. Erythropoietin decreased Hamp mRNA, but Rgmc expression was unchanged. Hamp mRNA level decreased after birth by four orders of magnitude, without significant changes in Rgmc expression. Administration of LPS elevated Hamp mRNA levels, while markedly decreasing hepatic Rgmc mRNA levels (to ~ 5 % after 6 hours). The responses of Hamp and Rgmc were quite different and suggested that human HJV expression could be modulated by inflammation.

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