DJ-1 promotes angiogenesis and osteogenesis by activating FGF receptor-1 signaling

Nat Commun. 2012:3:1296. doi: 10.1038/ncomms2313.

Abstract

Communication between osteoblasts and endothelial cells is essential for bone fracture repair, but the molecular identities of such communicating factors are not well defined. Here we identify DJ-1 as a novel mediator of the cross-talk between osteoblasts and endothelial cells through an unbiased screening of molecules secreted from human mesenchymal stem cells during osteogenesis. We show that DJ-1 stimulates the differentiation of human mesenchymal stem cells to osteoblasts and that DJ-1 induces angiogenesis in endothelial cells through activation of fibroblast growth factor receptor-1 signalling. In a rodent model of bone fracture repair, extracellular application of DJ-1 enhances bone regeneration in vivo by stimulating the formation of blood vessels and new bones. Both these effects are blocked by antagonizing fibroblast growth factor receptor-1 signalling. These findings uncover previously undefined extracellular roles of DJ-1 to promote angiogenesis and osteogenesis, suggesting DJ-1 may have therapeutic potential to stimulate bone regeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Regeneration / physiology
  • Cell Differentiation / physiology
  • Cell Line
  • Humans
  • Intracellular Signaling Peptides and Proteins / physiology*
  • Male
  • Mesenchymal Stem Cells / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neovascularization, Physiologic / physiology*
  • Nuclear Proteins / physiology*
  • Oncogene Proteins / physiology*
  • Osteoblasts / physiology
  • Osteogenesis / physiology*
  • Protein Deglycase DJ-1
  • Rats

Substances

  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • Oncogene Proteins
  • PGAP2 protein, human
  • PARK7 protein, human
  • Protein Deglycase DJ-1