Cellular Hypoxia Promotes Heterotopic Ossification by Amplifying BMP Signaling

J Bone Miner Res. 2016 Sep;31(9):1652-65. doi: 10.1002/jbmr.2848. Epub 2016 Apr 20.

Abstract

Hypoxia and inflammation are implicated in the episodic induction of heterotopic endochondral ossification (HEO); however, the molecular mechanisms are unknown. HIF-1α integrates the cellular response to both hypoxia and inflammation and is a prime candidate for regulating HEO. We investigated the role of hypoxia and HIF-1α in fibrodysplasia ossificans progressiva (FOP), the most catastrophic form of HEO in humans. We found that HIF-1α increases the intensity and duration of canonical bone morphogenetic protein (BMP) signaling through Rabaptin 5 (RABEP1)-mediated retention of Activin A receptor, type I (ACVR1), a BMP receptor, in the endosomal compartment of hypoxic connective tissue progenitor cells from patients with FOP. We further show that early inflammatory FOP lesions in humans and in a mouse model are markedly hypoxic, and inhibition of HIF-1α by genetic or pharmacologic means restores canonical BMP signaling to normoxic levels in human FOP cells and profoundly reduces HEO in a constitutively active Acvr1(Q207D/+) mouse model of FOP. Thus, an inflammation and cellular oxygen-sensing mechanism that modulates intracellular retention of a mutant BMP receptor determines, in part, its pathologic activity in FOP. Our study provides critical insight into a previously unrecognized role of HIF-1α in the hypoxic amplification of BMP signaling and in the episodic induction of HEO in FOP and further identifies HIF-1α as a therapeutic target for FOP and perhaps nongenetic forms of HEO. © 2016 American Society for Bone and Mineral Research.

Keywords: CELL/TISSUE SIGNALING; FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; PRECLINICAL STUDIES.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activin Receptors, Type I / metabolism
  • Animals
  • Bone Morphogenetic Proteins / metabolism*
  • Cell Hypoxia
  • Chondrogenesis
  • Disease Models, Animal
  • Endosomes / metabolism
  • Female
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Inflammation / pathology
  • Ligands
  • Male
  • Mice, Transgenic
  • Models, Biological
  • Myositis Ossificans / pathology
  • Ossification, Heterotopic / metabolism*
  • Ossification, Heterotopic / pathology*
  • Signal Transduction*
  • Stem Cells / metabolism
  • Stem Cells / pathology
  • Tooth Exfoliation / pathology
  • Tooth, Deciduous / pathology

Substances

  • Bone Morphogenetic Proteins
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Ligands
  • Activin Receptors, Type I