Combined degenerative and regenerative remodeling responses of the mandibular condyle to experimentally induced disordered occlusion

Am J Orthod Dentofacial Orthop. 2013 Jan;143(1):69-76. doi: 10.1016/j.ajodo.2012.08.024.

Abstract

Introduction: The purposes of this research were to investigate the long-term responses of mandibular condylar cartilage to experimentally induced disordered occlusion and to evaluate changes in the expression of the SDF-1/CXCR4 axis.

Methods: Experimentally induced disordered occlusions were created in 8-week-old female Sprague-Dawley rats by orthodontic methods. After 24 weeks, remodeling of the mandibular condylar cartilage was assessed by hematoxylin and eosin staining. Protein and mRNA expression of SDF-1, CXCR4, MMP9, IL6, OPG, and RANKL were investigated by means of immunohistochemical staining and real-time polymerase chain reaction.

Results: Obvious cartilage degenerative remodeling responses were observed; they appeared as uneven distributions of cellular disposition, loss of cartilage surface integrity, and cell-free areas. Regenerative responses presenting as thickening of the whole and the calcified cartilage layers in the experimental group were also observed. Compared with the age-matched controls, the protein and mRNA levels of SDF-1, CXCR4, MMP9, IL6, and OPG, but not RANKL, were increased in the experimental group (all, P <0.05). In addition, the mRNA level of RANKL/OPG showed a decreasing trend in the experimental group compared with the age-matched controls (P = 0.052).

Conclusions: This study demonstrated that long-term experimentally induced disordered occlusion leads to a combined response in degeneration and regeneration of mandibular cartilage, accompanied by active interaction of the SDF-1/CXCR4 axis and local upregulation of MMP9, IL6, and OPG.

MeSH terms

  • Animals
  • Bone Remodeling
  • Cartilage, Articular / metabolism*
  • Cartilage, Articular / pathology*
  • Chemokine CXCL12 / metabolism
  • Female
  • Interleukin-6 / metabolism
  • Malocclusion / complications*
  • Mandibular Condyle / physiopathology*
  • Matrix Metalloproteinase 9 / metabolism
  • Osteoarthritis / etiology
  • Osteoarthritis / pathology*
  • Osteoprotegerin / metabolism
  • RANK Ligand / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, CXCR4 / metabolism
  • Regeneration
  • Temporomandibular Joint Disorders / etiology
  • Temporomandibular Joint Disorders / pathology*

Substances

  • CXCL12 protein, rat
  • Chemokine CXCL12
  • Cxcr4 protein, rat
  • Interleukin-6
  • Osteoprotegerin
  • RANK Ligand
  • Receptors, CXCR4
  • Matrix Metalloproteinase 9