Transglutaminase-2 differently regulates cartilage destruction and osteophyte formation in a surgical model of osteoarthritis

Amino Acids. 2009 Apr;36(4):755-63. doi: 10.1007/s00726-008-0129-3. Epub 2008 Jun 27.

Abstract

Osteoarthritis is a progressive joint disease characterized by cartilage degradation and bone remodeling. Transglutaminases catalyze a calcium-dependent transamidation reaction that produces covalent cross-linking of available substrate glutamine residues and modifies the extracellular matrix. Increased transglutaminases-mediated activity is reported in osteoarthritis, but the relative contribution of transglutaminases-2 (TG2) is uncertain. We describe TG2 expression in human femoral osteoarthritis and in wild-type and homozygous TG2 knockout mice after surgically-induced knee joint instability. Increased TG2 levels were observed in human and wild-type murine osteoarthritic cartilage compared to the respective controls. Histomorphometrical but not X-ray investigation documented in osteoarthritic TG2 knockout mice reduced cartilage destruction and an increased osteophyte formation compared to wild-type mice. These differences were associated with increased TGFbeta-1 expression. In addition to confirming its important role in osteoarthritis development, our results demonstrated that TG2 expression differently influences cartilage destruction and bone remodeling, suggesting new targeted TG2-related therapeutic strategies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cartilage / enzymology
  • Cartilage / metabolism*
  • Cartilage / pathology
  • Disease Models, Animal
  • Female
  • GTP-Binding Proteins / biosynthesis
  • GTP-Binding Proteins / metabolism*
  • Humans
  • Male
  • Mice
  • Mice, Knockout
  • Osteoarthritis / enzymology
  • Osteoarthritis / metabolism*
  • Osteoarthritis / surgery*
  • Osteophyte / enzymology
  • Osteophyte / metabolism*
  • Osteophyte / pathology
  • Protein Glutamine gamma Glutamyltransferase 2
  • Transforming Growth Factor beta1 / biosynthesis
  • Transglutaminases / biosynthesis
  • Transglutaminases / metabolism*

Substances

  • Transforming Growth Factor beta1
  • Protein Glutamine gamma Glutamyltransferase 2
  • Transglutaminases
  • GTP-Binding Proteins