HIF hydroxylase pathways in cardiovascular physiology and medicine

Circ Res. 2015 Jun 19;117(1):65-79. doi: 10.1161/CIRCRESAHA.117.305109.

Abstract

Hypoxia inducible factors (HIFs) are α/β heterodimeric transcription factors that direct multiple cellular and systemic responses in response to changes in oxygen availability. The oxygen sensitive signal is generated by a series of iron and 2-oxoglutarate-dependent dioxygenases that catalyze post-translational hydroxylation of specific prolyl and asparaginyl residues in HIFα subunits and thereby promote their destruction and inactivation in the presence of oxygen. In hypoxia, these processes are suppressed allowing HIF to activate a massive transcriptional cascade. Elucidation of these pathways has opened several new fields of cardiovascular research. Here, we review the role of HIF hydroxylase pathways in cardiac development and in cardiovascular control. We also consider the current status, opportunities, and challenges of therapeutic modulation of HIF hydroxylases in the therapy of cardiovascular disease.

Keywords: dioxygenases; hypoxia; hypoxia inducible factor; prolyl hydroxylases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adaptation, Physiological
  • Altitude
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / deficiency
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cardiovascular Diseases / drug therapy
  • Cardiovascular Diseases / enzymology
  • Cardiovascular Diseases / metabolism*
  • Cardiovascular System / enzymology
  • Cardiovascular System / metabolism*
  • Cell Hypoxia
  • Heart / embryology
  • Heart Defects, Congenital / embryology
  • Heart Defects, Congenital / enzymology
  • Humans
  • Hydroxylation
  • Hypertension, Pulmonary / metabolism
  • Hypoxia / metabolism
  • Hypoxia-Inducible Factor 1, alpha Subunit / deficiency
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Hypoxia-Inducible Factor-Proline Dioxygenases / antagonists & inhibitors
  • Hypoxia-Inducible Factor-Proline Dioxygenases / deficiency
  • Hypoxia-Inducible Factor-Proline Dioxygenases / genetics
  • Hypoxia-Inducible Factor-Proline Dioxygenases / physiology*
  • Iron / physiology
  • Ischemic Preconditioning, Myocardial
  • Mice
  • Mixed Function Oxygenases / physiology
  • Oxygen / metabolism
  • Polycythemia / enzymology
  • Polycythemia / genetics
  • Protein Isoforms
  • Protein Processing, Post-Translational
  • Repressor Proteins / physiology
  • Von Hippel-Lindau Tumor Suppressor Protein / genetics
  • Von Hippel-Lindau Tumor Suppressor Protein / metabolism

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Protein Isoforms
  • Repressor Proteins
  • endothelial PAS domain-containing protein 1
  • Iron
  • Mixed Function Oxygenases
  • HIF1AN protein, human
  • EGLN1 protein, human
  • Hypoxia-Inducible Factor-Proline Dioxygenases
  • Von Hippel-Lindau Tumor Suppressor Protein
  • Oxygen