Ectopic expression of cyclooxygenase-2-induced dedifferentiation in articular chondrocytes

Exp Mol Med. 2008 Dec 31;40(6):721-7. doi: 10.3858/emm.2008.40.6.721.

Abstract

Cyclooxygenase-2 (COX-2) is known to modulate bone metabolism, including bone formation and resorption. Because cartilage serves as a template for endochondral bone formation and because cartilage development is initiated by the differentiation of mesenchymal cells into chondrocytes (Ahrens et al., 1977; Sandell and Adler, 1999; Solursh, 1989), it is of interest to know whether COX-2 expression affect chondrocyte differentiation. Therefore, we investigated the effects of COX-2 protein on differentiation in rabbit articular chondrocyte and chick limb bud mesenchymal cells. Overexpression of COX-2 protein was induced by the COX-2 cDNA transfection. Ectopic expression of COX-2 was sufficient to causes dedifferentiation in articular chondrocytes as determined by the expression of type II collagen via Alcian blue staining and Western blot. Also, COX-2 overexpression caused suppression of SOX-9 expression, a major transcription factor that regulates type II collagen expression, as indicated by the Western blot and RT-PCR. We further examined ectopic expression of COX-2 in chondrifying mesenchymal cells. As expected, COX-2 cDNA transfection blocked cartilage nodule formation as determined by Alcian blue staining. Our results collectively suggest that COX-2 overexpression causes dedifferentiation in articular chondrocytes and inhibits chondrogenic differentiation of mesenchymal cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cartilage, Articular / cytology
  • Cell Differentiation
  • Cells, Cultured
  • Chick Embryo
  • Chondrocytes / cytology*
  • Chondrocytes / enzymology
  • Chondrogenesis
  • Collagen Type II / metabolism
  • Cyclooxygenase 2 / biosynthesis*
  • Cyclooxygenase 2 / genetics
  • Interleukin-1beta / pharmacology
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / enzymology
  • Rabbits
  • SOX9 Transcription Factor / metabolism

Substances

  • Collagen Type II
  • Interleukin-1beta
  • SOX9 Transcription Factor
  • Cyclooxygenase 2