Wnt/beta-catenin signaling stimulates matrix catabolic genes and activity in articular chondrocytes: its possible role in joint degeneration

Lab Invest. 2008 Mar;88(3):264-74. doi: 10.1038/labinvest.3700747. Epub 2008 Jan 28.

Abstract

A fine balance between anabolic and catabolic mechanisms maintains extracellular matrix homeostasis in articular cartilage, and shifts toward degradation are associated with joint conditions such as osteoarthritis. To test the possible involvement, relevance and significance of the Wnt/beta-catenin-signaling pathway in those catabolic shifts, rabbit articular chondrocyte cultures were subjected to experimental activation of beta-catenin signaling by Wnt3A treatment or forced expression of constitutive-active beta-catenin (CA-beta-catenin). Both interventions provoked strong gelatinase activity and stimulated gene expression of matrix metalloprotease-3 and -13 and a disintegrin-like and metalloprotease with thrombospondin motif (ADAMTS)-4 and -5 proteases. Furthermore, Wnt3A treatment additively enhanced the effects of intereukin-1beta, a well-known catabolic culprit of proteoglycan matrix loss. To determine whether Wnt/beta-catenin signaling is associated with age-associated osteoarthritic changes in articular cartilage in vivo, we analyzed the presence and intracellular distribution of beta-catenin in a spontaneous guinea pig osteoarthritis model. Healthy articular chondrocytes in young guinea pig knees contained barely detectable levels of beta-catenin. In contrast, the protein was highly abundant in osteoarthritic-like chondrocytes present in older guinea pig joints, and was localized not only in the cytoplasm but also the nucleus, a clear reflection of activated Wnt signaling. These and other data suggest that Wnt/beta-catenin signaling is a powerful stimulator of chondrocyte matrix catabolic action and may be part of mechanisms leading to excessive remodeling and degradation of cartilage matrix in age-associated joint pathologies.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • ADAM Proteins / genetics
  • ADAM Proteins / metabolism
  • Adenoviridae / genetics
  • Animals
  • Cartilage, Articular / drug effects
  • Cartilage, Articular / metabolism*
  • Cell Culture Techniques
  • Cell Nucleus / metabolism
  • Cell Separation / methods
  • Cells, Cultured
  • Chondrocytes / cytology
  • Chondrocytes / metabolism*
  • Culture Media, Conditioned
  • Cytoplasm / metabolism
  • Disease Models, Animal
  • Epitopes
  • Extracellular Matrix / genetics
  • Extracellular Matrix / metabolism
  • Female
  • Genes, Reporter
  • Guinea Pigs
  • Hemagglutinins / metabolism
  • Immunohistochemistry
  • Interleukin-1beta / metabolism
  • Joints / pathology*
  • L Cells
  • Luciferases / analysis
  • Luciferases / metabolism
  • Matrix Metalloproteinase 13 / genetics
  • Matrix Metalloproteinase 13 / metabolism
  • Matrix Metalloproteinase 3 / genetics
  • Matrix Metalloproteinase 3 / metabolism
  • Mice
  • Osteoarthritis / pathology
  • Proteoglycans / analysis
  • Proteoglycans / metabolism
  • Rabbits
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / pharmacology
  • Signal Transduction*
  • Transfection
  • Trypsin / pharmacology
  • Wnt Proteins / genetics
  • Wnt Proteins / metabolism
  • Wnt Proteins / physiology*
  • beta Catenin

Substances

  • Culture Media, Conditioned
  • Epitopes
  • Hemagglutinins
  • Interleukin-1beta
  • Proteoglycans
  • Recombinant Proteins
  • Wnt Proteins
  • beta Catenin
  • Luciferases
  • Trypsin
  • ADAM Proteins
  • Matrix Metalloproteinase 13
  • Matrix Metalloproteinase 3