IL-10 overexpression differentially affects cartilage matrix gene expression in response to TNF-alpha in human articular chondrocytes in vitro

Cytokine. 2008 Dec;44(3):377-85. doi: 10.1016/j.cyto.2008.10.012. Epub 2008 Nov 20.

Abstract

Cartilage-specific extracellular matrix synthesis is the prerequisite for chondrocyte survival and cartilage function, but is affected by the pro-inflammatory cytokine TNF-alpha in arthritis. The aim of the present study was to characterize whether the immunoregulatory cytokine IL-10 might modulate cartilage matrix and cytokine expression in response to TNF-alpha. Primary human articular chondrocytes were treated with either recombinant IL-10, TNF-alpha or a combination of both (at 10ng/mL each) or transduced with an adenoviral vector overexpressing human IL-10 and subsequently stimulated with 10ng/ml TNF-alpha for 6 or 24h. The effects of IL-10 on the cartilage-specific matrix proteins collagen type II, aggrecan, matrix-metalloproteinases (MMP)-3, -13 and pro-inflammatory cytokines were evaluated by real-time RT-PCR and immunohistochemistry. Transduced chondrocytes overexpressed high levels of IL-10 which significantly up-regulated collagen type II expression. TNF-alpha suppressed collagen type II and aggrecan, but increased MMP and cytokine expression in chondrocytes compared to the non-stimulated controls. The TNF-alpha mediated down-regulation of aggrecan expression was significantly antagonized by IL-10 overexpression, whereas the suppression of collagen type II was barely affected. The MMP-13 and IL-1beta expression by TNF-alpha was slightly reduced by IL-10. These results suggest that IL-10 overexpression modulates some catabolic features of TNF-alpha in chondrocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics
  • Adenoviridae / metabolism
  • Aged
  • Aged, 80 and over
  • Arteries / metabolism
  • Cartilage Oligomeric Matrix Protein
  • Cells, Cultured
  • Chondrocytes / drug effects*
  • Chondrocytes / metabolism*
  • Chondrocytes / ultrastructure
  • Collagen Type II / genetics
  • Collagen Type II / metabolism
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / metabolism*
  • Gene Expression Regulation / drug effects*
  • Gene Expression Regulation / genetics*
  • Genetic Vectors / genetics
  • Glycoproteins / genetics
  • Glycoproteins / metabolism*
  • Humans
  • Interleukin-10 / genetics
  • Interleukin-10 / metabolism*
  • Matrilin Proteins
  • Matrix Metalloproteinase 13 / genetics
  • Matrix Metalloproteinase 13 / metabolism
  • Matrix Metalloproteinase 3 / genetics
  • Matrix Metalloproteinase 3 / metabolism
  • Microscopy, Electron, Transmission
  • Middle Aged
  • RNA, Messenger / genetics
  • Tumor Necrosis Factor-alpha

Substances

  • Cartilage Oligomeric Matrix Protein
  • Collagen Type II
  • Extracellular Matrix Proteins
  • Glycoproteins
  • Matrilin Proteins
  • RNA, Messenger
  • TSP5 protein, human
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Matrix Metalloproteinase 13
  • Matrix Metalloproteinase 3