BMPER protein is a negative regulator of hepcidin and is up-regulated in hypotransferrinemic mice Academic Article uri icon

Overview

MeSH Major

  • Antimicrobial Cationic Peptides
  • Carrier Proteins
  • Iron
  • Liver
  • Transferrin
  • Up-Regulation

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 (Trf(hpx/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.

publication date

  • February 3, 2012

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC3281740

Digital Object Identifier (DOI)

  • 10.1074/jbc.M111.310789

PubMed ID

  • 22144676

Additional Document Info

start page

  • 4099

end page

  • 106

volume

  • 287

number

  • 6