Unilateral anterior crossbite induces aberrant mineral deposition in degenerative temporomandibular cartilage in rats

Osteoarthritis Cartilage. 2016 May;24(5):921-31. doi: 10.1016/j.joca.2015.12.009. Epub 2015 Dec 31.

Abstract

Objective: To investigate whether mechanical stress induces mineral deposits that contribute to matrix degradation at the onset of osteoarthritis (OA) in temporomandibular joint (TMJ) cartilage.

Design: Female Spraguee-Dawley rats were subjected to an unilateral anterior crossbite (UAC) procedure. Histology, electron microscopy, and energy dispersive spectrometer (EDS) were used to examine cartilage matrix structures and composition of mineral deposit in the affected TMJ cartilage. Protein and/or RNA expression of phenotypic markers and mineralization modulators and matrix degradation was analyzed by immunohistochemistry and/or real-time PCR. Synthetic basic calcium phosphate (BCP) and calcium pyrophosphate dehydrate (CPPD) crystals were used to stimulate ATDC5 cells for their impact on cell differentiation and gene expression.

Results: Fragmented and disorganized collagen fibers, expanded fibrous spaces, and enhancement of matrix vesicle production and mineral deposition were observed in matrices surrounding hypertrophic chondrocytes in cartilage as early as 2-weeks post-UAC and exacerbated with time. The mineral deposits in TMJ cartilage at 12- and 20-weeks post-UAC had Ca/P ratios of 1.42 and 1.44, which are similar to the ratios for BCP. The expression of mineralization inhibitors, NPP1, ANK, CD73, and Matrix gla protein (MGP) was decreased from 2 to 8 weeks post-UAC, so were the chondrogenic markers, Col-2, Col-X and aggrecan. In contrast, the expression of tissue-nonspecific alkaline phosphatase (TNAP) and MMP13 was increased 4-weeks post-UAC. Treating ADTC5 cells with BCP crystals increased MMPs and ADAMTS5 expression, but reduced matrix production in a time-dependent manner.

Conclusion: UAC induces deposition of BCP-like minerals in osteoarthritic cartilage, which can stimulate matrix degradation by promoting the expression of cartilage-degrading enzymes to facilitate OA progression.

Keywords: BCP; CPPD; Calcium-crystal; Osteoarthritis (OA); Temporomandibular joint (TMJ).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium Phosphates / metabolism
  • Calcium Phosphates / pharmacology
  • Calcium Pyrophosphate / metabolism
  • Calcium Pyrophosphate / pharmacology
  • Cartilage Diseases / etiology*
  • Cartilage Diseases / pathology
  • Cartilage, Articular / metabolism
  • Cartilage, Articular / ultrastructure
  • Cell Differentiation / drug effects
  • Chondrocalcinosis / etiology*
  • Chondrocalcinosis / pathology
  • Chondrocytes / drug effects
  • Chondrocytes / pathology
  • Female
  • Malocclusion / complications*
  • Microscopy, Electron
  • Rats, Sprague-Dawley
  • Temporomandibular Joint / metabolism
  • Temporomandibular Joint / ultrastructure
  • Temporomandibular Joint Disorders / etiology*
  • Temporomandibular Joint Disorders / pathology

Substances

  • Calcium Phosphates
  • calcium phosphate
  • Calcium Pyrophosphate