Effects of dendritic polyglycerol sulfate on articular chondrocytes

Inflamm Res. 2015 Nov;64(11):917-28. doi: 10.1007/s00011-015-0875-0. Epub 2015 Sep 9.

Abstract

Introduction: Inflammatory processes driven by cytokines play a crucial role during osteoarthritis (OA) progression. Dendritic polyglycerol sulfate (dPGS) was analyzed in vitro for its effects on articular chondrocytes, cartilage and cytokines involved in the OA process.

Methods: The metabolic activity of cultured human articular chondrocytes stimulated for 24 h with dPGS (10(-3)-10(-6) mol/L) was monitored using AlamarBlue(®) assay. The dPGS uptake was studied using fluorescence labeled nanoparticles. Further, chondrocytes were either treated with 10(-6) M dPGS, TNFα (10 ng/mL) alone or with a combination of both. The influence on extracellular matrix components, pro- and anti-inflammatory cytokines, matrix metalloproteinase (MMP)1 and the anaphylatoxin receptor C3aR was analyzed by RTD-PCR, flow cytometry and ELISA.

Results: Even at higher dosages (10(-3) mol/L), dPGS did not influence chondrocytes viability. Uptake of dPGS was successfully monitored in human articular chondrocytes and synovial fibroblasts, penetration into cartilage chips was up to ~50 µm. Cellular treatment with dPGS had no effect on synthesis of pro-inflammatory cytokines TNFα and IL-6, but expression of the anti-inflammatory IL-10 was upregulated. Cotreatment with TNFα and dPGS reduced the TNFα level, while IL-1β, IL-6 and IL-10 expression did not change. Collagen type II gene expression was significantly reduced after preincubating cells with dPGS, but remained unaffected at the protein level.

Conclusion: Results indicate that dPGS could play a role in regulation of cytokines associated with the inflammatory aspect of OA progression.

Keywords: Chondrocytes; Cytokines; Nanoparticles; Synovial fibroblasts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Animals
  • Cartilage, Articular / cytology
  • Cell Line
  • Cells, Cultured
  • Chondrocytes / drug effects*
  • Chondrocytes / metabolism
  • Collagen Type II / genetics
  • Collagen Type II / metabolism
  • Cytokines / metabolism
  • Dendrimers / pharmacology*
  • Extracellular Matrix / metabolism
  • Female
  • Fibroblasts / metabolism
  • Gene Expression Regulation / drug effects
  • Glycerol / pharmacology*
  • Humans
  • Male
  • Mice
  • Middle Aged
  • Polymers / pharmacology*
  • Swine

Substances

  • Collagen Type II
  • Cytokines
  • Dendrimers
  • Polymers
  • polyglycerol
  • Glycerol