Hyaluronan differently modulates TLR-4 and the inflammatory response in mouse chondrocytes

Biofactors. 2012 Jan-Feb;38(1):69-76. doi: 10.1002/biof.202. Epub 2012 Jan 30.

Abstract

Hyaluronic acid (HA) may exert different action depending on its degree of polymerization. Small HA fragments induce proinflammatory responses, while highly polymerized HA exerts a protective effect in inflammatory pathologies such as rheumatoid arthritis. In both cases the toll-like receptor 4 (TLR-4) seems to be involved in the modulation of the inflammation process. The aim of this study was to investigate the influence of short HA oligosaccharides (HA 4-mers) and high molecular weight HA (HMWHA) in the inflammatory response in normal mouse chondrocytes. Messenger RNA and related protein levels were measured for TLR-4, tumor necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta), interleukin-6 (IL-6), and interleukin-18 (IL-18) in cells with and without the addition of HA. NF-kB activation was also evaluated. 4-mer HA treatment produced a significant up-regulation of all parameters considered while HMWHA did not exert any activity in untreated cells although it was able to reduce the effects of 4- mers HA significantly. Specific TLR-4 small interference RNA (siRNA) was used to confirm TLR-4 as the target of HA action. This study suggests that HA may modulate proinflammatory cytokines via its different degree of polymerization and inflammatory action may be modulated as a result of the interaction between HA and TLR-4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cartilage, Articular / cytology
  • Cell Shape
  • Cell Survival / drug effects
  • Cells, Cultured
  • Chondrocytes / drug effects*
  • Chondrocytes / metabolism
  • Cytokines / genetics
  • Cytokines / metabolism
  • Hyaluronic Acid / pharmacology*
  • Inflammation Mediators / metabolism
  • Male
  • Mice
  • Mice, Inbred DBA
  • NF-kappa B / metabolism
  • Protein Binding
  • Protein Transport
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / metabolism*
  • Transcription, Genetic

Substances

  • Cytokines
  • Inflammation Mediators
  • NF-kappa B
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • Hyaluronic Acid