Insulin-like growth factor-1 engaged in the mandibular condylar cartilage degeneration induced by experimental unilateral anterior crossbite

Arch Oral Biol. 2019 Feb:98:17-25. doi: 10.1016/j.archoralbio.2018.11.002. Epub 2018 Nov 3.

Abstract

Objective: To investigate the changes in insulin-like growth factor-1 (IGF-1) expression levels in the degenerative mandibular condylar cartilage.

Design: Thirty-six rats were divided into the unilateral anterior crossbite and control groups. The expression levels of IGF-1; IGF-1 receptor (IGF-1R); IGF-binding protein-3 and -5 (IGFBP-3 and -5); proliferating cell nuclear antigen (PCNA); aggrecan; type-I, -II, -VI, and -X collagen; tissue inhibitor of metalloproteinases-1 and -3 (TIMP-1 and -3); metalloproteinases of matrix metalloproteinases-3 and-13 (MMP-3 and -13); a disintegrin and metalloproteinase thrombospondin-4 and -5 (ADAMTS-4 and -5); alkaline phosphatase (ALP); β-glucuronidase; and N-acetyl-β-glucosaminidase in the mandibular condylar cartilage were assessed.

Results: The protein expression levels of IGF-1and IGF-1R were increased from week 4 in the unilateral anterior crossbite group. The mRNA expression level of IGFBP-3 and -5 was upregulated from week 4 and week 2, respectively; that of IGFBP-3 was downregulated at week 8; and that of PCNA, type-II collagen, type-X collagen, aggrecan, TIMP-1, and TIMP-3 was downregulated, whereas that of MMP-3, MMP-13, ADAMTS-4, ADAMTS-5, β-glucuronidase, and N-acetyl-β-glucosaminidase were upregulated from week 2. The positive area size of type-I collagen was increased and that of type VI collagen was decreased from week 2. The positive area size of type X collagen was increased at week 2 but decreased at week 8. The percentage of ALP-positive cells was increased from week 4.

Conclusions: Unilateral anterior crossbite stimulated the multifarious expression of IGF-1 and IGFBP, which may be linked to chondrocyte proliferation and differentiation in the mandibular condylar cartilage that showed progressive degeneration.

Keywords: Articular cartilage; Chondrocyte; Dental occlusion; Insulin-like growth factor-1 (IGF-1); Osteoarthritis; Temporomandibular joint.

MeSH terms

  • ADAMTS4 Protein / metabolism
  • ADAMTS5 Protein / metabolism
  • Aggrecans / metabolism
  • Alkaline Phosphatase / metabolism
  • Animals
  • Cartilage Diseases / etiology*
  • Cartilage, Articular / pathology*
  • Chondrocytes / pathology
  • Collagen / metabolism
  • Disease Models, Animal
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation, Enzymologic
  • Glucuronidase / metabolism
  • Insulin-Like Growth Factor Binding Protein 3 / metabolism
  • Insulin-Like Growth Factor Binding Protein 5 / metabolism
  • Insulin-Like Growth Factor I / metabolism*
  • Malocclusion / complications*
  • Mandibular Condyle / metabolism*
  • Mandibular Condyle / pathology*
  • Matrix Metalloproteinase 13 / metabolism
  • Matrix Metalloproteinase 3 / metabolism
  • Proliferating Cell Nuclear Antigen / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, IGF Type 1 / metabolism
  • Temporomandibular Joint Disorders / etiology*
  • Tissue Inhibitor of Metalloproteinase-1 / metabolism
  • Tissue Inhibitor of Metalloproteinase-3 / metabolism
  • Up-Regulation

Substances

  • Aggrecans
  • Insulin-Like Growth Factor Binding Protein 3
  • Insulin-Like Growth Factor Binding Protein 5
  • Proliferating Cell Nuclear Antigen
  • Tissue Inhibitor of Metalloproteinase-1
  • Tissue Inhibitor of Metalloproteinase-3
  • insulin-like growth factor-1, rat
  • Insulin-Like Growth Factor I
  • Collagen
  • Receptor, IGF Type 1
  • Alkaline Phosphatase
  • Glucuronidase
  • ADAMTS5 Protein
  • Matrix Metalloproteinase 13
  • Matrix Metalloproteinase 3
  • ADAMTS4 Protein