Hypoxia induced downregulation of hepcidin is mediated by platelet derived growth factor BB

Gut. 2014 Dec;63(12):1951-9. doi: 10.1136/gutjnl-2013-305317. Epub 2014 Mar 5.

Abstract

Objective: Hypoxia affects body iron homeostasis; however, the underlying mechanisms are incompletely understood.

Design: Using a standardised hypoxia chamber, 23 healthy volunteers were subjected to hypoxic conditions, equivalent to an altitude of 5600 m, for 6 h. Subsequent experiments were performed in C57BL/6 mice, CREB-H knockout mice, primary hepatocytes and HepG2 cells.

Results: Exposure of subjects to hypoxia resulted in a significant decrease of serum levels of the master regulator of iron homeostasis hepcidin and elevated concentrations of platelet derived growth factor (PDGF)-BB. Using correlation analysis, we identified PDGF-BB to be associated with hypoxia mediated hepcidin repression in humans. We then exposed mice to hypoxia using a standardised chamber and observed downregulation of hepatic hepcidin mRNA expression that was paralleled by elevated serum PDGF-BB protein concentrations and higher serum iron levels as compared with mice housed under normoxic conditions. PDGF-BB treatment in vitro and in vivo resulted in suppression of both steady state and BMP6 inducible hepcidin expression. Mechanistically, PDGF-BB inhibits hepcidin transcription by downregulating the protein expression of the transcription factors CREB and CREB-H, and pharmacological blockade or genetic ablation of these pathways abrogated the effects of PDGF-BB toward hepcidin expression.

Conclusions: Hypoxia decreases hepatic hepcidin expression by a novel regulatory pathway exerted via PDGF-BB, leading to increased availability of circulating iron that can be used for erythropoiesis.

Keywords: IRON METABOLISM; OXIDATIVE METABOLISM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Becaplermin
  • Disease Models, Animal
  • Down-Regulation
  • Erythropoiesis / physiology
  • Female
  • Healthy Volunteers
  • Hematologic Agents / pharmacology
  • Hep G2 Cells
  • Hepcidins / metabolism*
  • Humans
  • Hypoxia / etiology
  • Hypoxia / metabolism*
  • Iron / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Platelet-Derived Growth Factor / metabolism*
  • Proto-Oncogene Proteins c-sis / pharmacology*

Substances

  • Hematologic Agents
  • Hepcidins
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Proteins c-sis
  • Becaplermin
  • Iron