Accelerated osteoarthritis in the temporomandibular joint of biglycan/fibromodulin double-deficient mice

• Published in: Osteoarthritis and cartilage Vol. 13; no. 9; pp. 817 - 827
• Main Authors: Wadhwa, S., Embree, M.C., Kilts, T., Young, M.F., Ameye, L.G.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.09.2005
• Subjects: Animals; Biglycan; Biomarkers - analysis; Breeding; Cartilage, Articular - pathology; Cell Proliferation; Disease Progression; Extracellular Matrix Proteins - analysis; Extracellular Matrix Proteins - genetics; Female; Fibromodulin; Immunohistochemistry; Male; Mice; Mice, Knockout; Osteoarthritis; Osteoarthritis - pathology; Proliferating Cell Nuclear Antigen - analysis; Proliferation; Proteoglycans - analysis; Proteoglycans - genetics; Staining and Labeling; Temporomandibular joint (TMJ); Temporomandibular Joint Disorders - pathology; Fibromodulin; Biglycan; Mice; Temporomandibular joint (TMJ); Proliferation; Osteoarthritis
• ISSN: 1063-4584; 1522-9653
• DOI: 10.1016/j.joca.2005.04.016

To investigate whether the absence of biglycan and fibromodulin, two proteoglycans expressed in cartilage, bone and tendon, resulted in accelerated osteoarthritis in the temporomandibular joint (TMJ). Histological sections of TMJ from 3-, 6-, 9- and 18-month-old wild-type (WT) and biglycan/fibromodulin double-deficient (DKO) mice were compared. Immunostainings for biglycan, fibromodulin and proliferating cell nuclear antigen (PCNA) were performed. Biglycan and fibromodulin were highly expressed in the disc and articular cartilage of the TMJ. At 3 months of age, both WT and DKO presented early signs of cartilage degeneration visible as small acellular areas under the articular surfaces and superficial waving. From 6 months of age, DKOs developed accelerated osteoarthritis compared to WT. At 6 months, small vertical clefts in the condylar cartilage and partial disruption of the disk were visible in the DKO. In addition, chondrocytes had lost their regular columnar organization to form clusters. At 9 months, these differences were even more pronounced. At 18 months, extended cartilage erosion was visible in DKOs when by comparison the thickness of the articular cartilage in WT controls was basically intact. PCNA staining was stronger in 3-month-old WT TMJ fibrocartilage than in 3-month-old DKO TMJ fibrocartilage suggesting that chondrocyte proliferation might be impaired in DKOs. The biglycan/fibromodulin double knock-out mouse constitutes a useful animal model to decipher the pathobiology of osteoarthritis in the TMJ.