Hyaluronan suppresses mechanical stress-induced expression of catabolic enzymes by human chondrocytes via inhibition of IL-1β production and subsequent NF-κB activation

Inflamm Res. 2015 Apr;64(3-4):243-52. doi: 10.1007/s00011-015-0804-2. Epub 2015 Feb 19.

Abstract

Objective: To investigate the inhibitory effect of hyaluronan (HA) on mechanical stress- induced expression of a disintegrin and metalloproteinase with thrombospondin type 1 motifs (ADAMTS)-4, -5 and matrix metalloproteinase (MMP)-13 by human chondrocytes.

Materials and methods: Normal human articular chondrocytes were pre-incubated with or without 1.0 mg/mL HA (2700 kDa) for 12 h at 37 °C in stretch chambers, then they were exposed to uni-axial cyclic tensile strain (CTS, 0.5 Hz, 10% elongation). The expression of ADAMTS-4, -5, and MMP-13 were analyzed by real-time polymerase chain reaction and Immunocytochemistry. The concentration of IL-1β in the supernatant was measured using enzyme-linked immunosorbent assay (ELISA). The nuclear translocation of runt-related transcription factor 2 (RUNX-2) and nuclear factor-κB (NF-κB) was examined by ELISA and immunocytochemistry, and phosphorylation of NF-κB was examined by western blotting.

Results: HA inhibited mRNA expression of ADAMTS-4, -5, and MMP13 after 24 h CTS via inhibition of IL-1β secretion and NF-κB activation. However, HA failed to inhibit CTS-induced RUNX-2 expression and subsequent expression of ADAMTS-5 and MMP-13 1 h after CTS.

Conclusions: Our results demonstrated that HA significantly suppressed mechanical stress-induced expression of catabolic proteases by inhibition of the NF-κB-IL-1β pathway, but did not suppress mechanical stress-induced RUNX-2 signaling.

MeSH terms

  • ADAM Proteins / antagonists & inhibitors*
  • ADAM Proteins / metabolism
  • ADAMTS4 Protein
  • ADAMTS5 Protein
  • Adolescent
  • Adult
  • Cells, Cultured
  • Chondrocytes / cytology
  • Chondrocytes / drug effects*
  • Chondrocytes / metabolism
  • Core Binding Factor Alpha 1 Subunit / metabolism
  • Disintegrins / antagonists & inhibitors*
  • Disintegrins / metabolism
  • Humans
  • Hyaluronic Acid / pharmacology*
  • In Vitro Techniques
  • Interleukin-1beta / antagonists & inhibitors
  • Interleukin-1beta / metabolism
  • Matrix Metalloproteinase 13 / metabolism
  • NF-kappa B / metabolism
  • Procollagen N-Endopeptidase / antagonists & inhibitors*
  • Procollagen N-Endopeptidase / metabolism
  • RNA, Messenger / antagonists & inhibitors
  • RNA, Messenger / metabolism
  • Signal Transduction / drug effects
  • Stress, Mechanical*

Substances

  • Core Binding Factor Alpha 1 Subunit
  • Disintegrins
  • Interleukin-1beta
  • NF-kappa B
  • RNA, Messenger
  • RUNX2 protein, human
  • Hyaluronic Acid
  • ADAM Proteins
  • ADAMTS5 Protein
  • ADAMTS5 protein, human
  • Matrix Metalloproteinase 13
  • Procollagen N-Endopeptidase
  • ADAMTS4 Protein
  • ADAMTS4 protein, human