Pressure and inflammatory stimulation induced increase of cadherin-11 is mediated by PI3K/Akt pathway in synovial fibroblasts from temporomandibular joint

Osteoarthritis Cartilage. 2013 Oct;21(10):1605-12. doi: 10.1016/j.joca.2013.07.015. Epub 2013 Jul 31.

Abstract

Objective: The goal of the study was to investigate the expression of cadherin-11 in synovial fibroblasts (SFs) under mechanical or inflammatory stimuli, and its potential relationship with PI3K/Akt signaling pathway.

Methods: SFs separated from rat temporomandibular joint (TMJ) were treated with hydrostatic pressures (HP) of 30, 60, 90, and 120 kPa, as well as tumor necrosis factor-α (TNF-α) for 12, 24, 48, and 72 h. The location of cadherin-11 was observed by immunofluorescence microscopy, and its expression was detected by real-time PCR and Western blot. We also studied the activation of PI3K/Akt signaling pathway in SFs with HP or TNF-α stimulation.

Results: The results showed that increased expression of cadherin-11 could be found in the cell-cell contact site of SFs in response to HP and inflammatory stimulation. The mRNA and protein expression of cadherin-11 was positively correlated with the intensity of HP and the duration time of TNF-α treatment. Increased expression of vascular endothelial growth factor-D (VEGF-D) and activation of Akt were also found. Treatment with PI3K inhibitor LY294002 attenuated the pressure or inflammatory cytokine induction increases of cadherin-11, VEGF-D, and FGF-2 both in mRNA and protein levels.

Conclusions: These findings suggest that cadherin-11 may play important roles in SFs following exposure to mechanical loading and inflammatory stimulation. In addition, PI3K/Akt pathway was associated with pressure or inflammation-induced cadherin-11 expression, which may involve in the pathogenesis of temporomandibular diseases.

Keywords: Cadherin-11; Hydrostatic pressure; Synovial fibroblasts; TNF-α; Temporomandibular disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cadherins / biosynthesis*
  • Cadherins / genetics
  • Cells, Cultured
  • Chromones / pharmacology
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism*
  • Fibroblasts / physiology
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / physiology
  • Hydrostatic Pressure
  • Inflammation Mediators / pharmacology
  • Male
  • Mechanotransduction, Cellular / physiology
  • Morpholines / pharmacology
  • Phosphatidylinositol 3-Kinases / physiology
  • Phosphoinositide-3 Kinase Inhibitors
  • Proto-Oncogene Proteins c-akt / physiology
  • RNA, Messenger / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / physiology
  • Synovial Membrane / cytology*
  • Synovial Membrane / drug effects
  • Synovial Membrane / metabolism
  • Temporomandibular Joint / cytology*
  • Temporomandibular Joint / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Cadherins
  • Chromones
  • Inflammation Mediators
  • Morpholines
  • Phosphoinositide-3 Kinase Inhibitors
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • osteoblast cadherin
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • Proto-Oncogene Proteins c-akt