Osteochondral angiogenesis in rat mandibular condyles with osteoarthritis-like changes

Arch Oral Biol. 2012 Jun;57(6):620-9. doi: 10.1016/j.archoralbio.2011.12.006. Epub 2012 Jan 10.

Abstract

Objective: To investigate angiogenesis at the osteochondral junction and changes in expression of pro- and anti-angiogenic factors in rat mandibular condyles with osteoarthritis-like changes.

Methods: In order to evoke osteoarthritis-like lesions in mandibular condyles, disordered occlusion was created experimentally in rats. Osteochondral vascularity was assessed histologically at 20 and 24 weeks. Protein and mRNA levels of pro-angiogenic factors including vascular endothelial growth factor (VEGF), connective tissue growth factor (CTGF) and matrix metalloproteases 9 (MMP9), and anti-angiogenic factor chondromodulin-I (CHM-I) were investigated by means of immunohistochemical staining and real-time PCR.

Results: Osteochondral angiogenesis was demonstrated as increased numbers of vascular channels terminating in the calcified cartilage and non-calcified cartilage in 20- and 24-week experimental groups compared with controls (all P<0.05). In the experimental groups, VEGF, CTGF and MMP9 were highly expressed in the tissues adjacent to the osteochondral junction. However, CHM-I was more expressed in the superior but not deep hypertrophic chondrocytes. Compared to their age-matched controls, the protein levels of VEGF and CTGF were higher in 20-week experimental group, and the protein and mRNA levels of CTGF, MMP-9, and CHM-I increased in the 24-week experimental group (all P<0.05).

Conclusion: In the present rat model, osteochondral angiogenesis was observed in mandibular condyles with osteoarthritis-like changes, accompanied with local upregulation of VEGF, CTGF and MMP9. Although the increase in CHM-I may moderate pro-angiogenic factors effects in the superior cartilage, the deficiency of deep hypertrophic chondrocytes to express CHM-I may permit vascular invasion into condylar cartilage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Connective Tissue Growth Factor / metabolism
  • Female
  • Immunohistochemistry
  • Mandibular Condyle / blood supply*
  • Mandibular Condyle / metabolism*
  • Mandibular Condyle / pathology*
  • Matrix Metalloproteinase 9 / metabolism
  • Neovascularization, Pathologic / pathology*
  • Osteoarthritis / psychology*
  • Rats
  • Rats, Sprague-Dawley
  • Real-Time Polymerase Chain Reaction
  • Statistics, Nonparametric
  • Up-Regulation
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Biomarkers
  • Vascular Endothelial Growth Factor A
  • Connective Tissue Growth Factor
  • Matrix Metalloproteinase 9