Iron-regulatory gene expression during liver regeneration

Scand J Gastroenterol. 2012 May;47(5):591-600. doi: 10.3109/00365521.2012.661761. Epub 2012 Feb 27.

Abstract

Background: In rat, the first 18-24 h after partial hepatectomy (PH) are characterized by an acute-phase reaction, after which liver regeneration predominates. Interleukin-6 (IL-6) induces the iron hormone hepcidin, which blocks iron uptake and may compromise iron uptake in the growing liver. The expressions of hepcidin and the iron-regulatory pathway of hepcidin gene expression during the late phase of liver regeneration are unknown.

Aim: To characterize the expression pattern of hepcidin and the iron-sensing pathway of hepcidin regulation during liver regeneration.

Methods: Rats were subjected to PH or sham operation. Liver weights, number of S-phase nuclei, and serum levels of iron and IL-6 were determined. Messenger-RNA levels of hepcidin, ferritin, hemojuvelin, transferrin receptor 1 and 2, HFE, divalent metal transporter 1, ferroportin, and ceruloplasmin were determined with qPCR at different time points. Protein levels of STAT3 and SMAD4 were determined with western blot.

Results: During the acute-phase response, IL-6 release induced STAT3 protein and hepcidin mRNA, whereas mRNA levels of proteins in the iron-sensing pathway (HFE, hemojuvelin, and transferrin receptor 2) decreased. The mRNA levels of proteins involved in cellular iron uptake were increased and cellular iron export unchanged. During liver regeneration >24 h after PH, gene expressions in the iron-sensing pathway were continuously suppressed and hepcidin mRNA levels declined 3-7 days after surgery.

Conclusions: Hepcidin gene expression peaks during the acute-phase response, but a sustained down-regulation of the iron-sensing pathway of hepcidin regulation gradually reduces hepcidin gene expression until regeneration is complete, thereby promoting iron mobilization to the regenerating liver.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / genetics*
  • Antimicrobial Cationic Peptides / metabolism
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism
  • Ceruloplasmin / genetics
  • Ceruloplasmin / metabolism
  • GPI-Linked Proteins
  • Gene Expression
  • Hemochromatosis Protein
  • Hepatectomy
  • Hepcidins
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / metabolism
  • Interleukin-6 / blood
  • Iron / blood
  • Liver / anatomy & histology*
  • Liver / physiology
  • Liver Regeneration / genetics*
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Organ Size
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Inbred F344
  • Receptors, Transferrin / genetics
  • Receptors, Transferrin / metabolism
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction / genetics*
  • Smad4 Protein / genetics
  • Smad4 Protein / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Cation Transport Proteins
  • GPI-Linked Proteins
  • HFE protein, rat
  • Hamp protein, rat
  • Hemochromatosis Protein
  • Hepcidins
  • Histocompatibility Antigens Class I
  • Hjv protein, rat
  • Interleukin-6
  • Membrane Proteins
  • RNA, Messenger
  • Receptors, Transferrin
  • STAT3 Transcription Factor
  • Smad4 Protein
  • Smad4 protein, rat
  • Stat3 protein, rat
  • Tfr2 protein, rat
  • Tfrc protein, rat
  • metal transporting protein 1
  • solute carrier family 11- (proton-coupled divalent metal ion transporters), member 2
  • Iron
  • Ceruloplasmin