Hepcidin-2 in mouse urine as a candidate radiation-responsive molecule

J Radiat Res. 2016 Mar;57(2):142-9. doi: 10.1093/jrr/rrv098. Epub 2016 Jan 28.

Abstract

We used high-performance liquid chromatography to separate urine obtained from whole-body gamma-irradiated mice (4 Gy) before analyzing each fraction with matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry to identify radiation-responsive molecules. We identified two candidates: hepcidin antimicrobial peptide 2 (hepcidin-2) and peptide fragments of kidney androgen-regulated protein (KAP). We observed that peak increases of hepcidin-2 in urine were delayed in a dose-dependent manner (1 Gy and above); however, the amount of KAP peptide fragments showed no correlation with radiation dose. In addition, an increase in hepcidin-2 after exposure to relatively low radiation doses (0.25 and 0.5 Gy, respectively) was biphasic (at 8-48 h and 120-168 h, respectively, after irradiation). The increase in hepcidin-2 paralleled an increase in hepcidin-2 gene (Hamp2) mRNA levels in the liver. These results suggest that radiation exposure directly or indirectly induces urinary excretion of hepcidin-2 at least in part by the upregulation of Hamp2 mRNA in the liver.

Keywords: hepcidin-2; mass spectrometry; radiation-responsive molecules; urine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / urine
  • Dose-Response Relationship, Radiation
  • Gamma Rays*
  • Hepcidins / genetics
  • Hepcidins / urine*
  • Liver / metabolism
  • Liver / radiation effects
  • Male
  • Mice, Inbred C57BL
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Tandem Mass Spectrometry
  • Whole-Body Irradiation

Substances

  • Biomarkers
  • Hamp2 protein, mouse
  • Hepcidins
  • RNA, Messenger