Activities per year
Abstract
The BMP/SMAD4 pathway has major effects on liver hepcidin levels. Bone morphogenetic protein-binding endothelial cell precursor-derived regulator (Bmper), a known regulator of BMP signaling, was found to be overexpressed at the mRNA and protein levels in liver of genetically hypotransferrinemic mice (Trfhpx/hpx). Soluble BMPER peptide inhibited BMP2- and BMP6-dependent hepcidin promoter activity in both HepG2 and HuH7 cells. These effects correlated with reduced cellular levels of pSMAD1/5/8. Addition of BMPER peptide to primary human hepatocytes abolished the BMP2-dependent increase in hepcidin mRNA, whereas injection of Bmper peptide into mice resulted in reduced liver hepcidin and increased serum iron levels. Thus Bmper may play an important role in suppressing hepcidin production in hypotransferrinemic mice.
Original language | English |
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Pages (from-to) | 4099 - 4106 |
Number of pages | 8 |
Journal | Journal of Biological Chemistry |
Volume | 287 |
Issue number | 6 |
DOIs | |
Publication status | Published - 3 Feb 2012 |
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Dive into the research topics of 'BMPER Protein Is a Negative Regulator of Hepcidin and Is Up-regulated in Hypotransferrinemic Mice'. Together they form a unique fingerprint.Activities
- 1 Participation in conference
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International Bioiron Society
McKie, A. (Keynote/plenary speaker)
22 May 2011Activity: Participating in or organising an event › Participation in conference