Inhibitory Effects of Viscum coloratum Extract on IgE/Antigen-Activated Mast Cells and Mast Cell-Derived Inflammatory Mediator-Activated Chondrocytes

Molecules. 2016 Dec 28;22(1):37. doi: 10.3390/molecules22010037.

Abstract

The accumulation and infiltration of mast cells are found in osteoarthritic lesions in humans and rodents. Nonetheless, the roles of mast cells in osteoarthritis are almost unknown. Although Viscum coloratum has various beneficial actions, its effect on allergic and osteoarthritic responses is unknown. In this study, we established an in vitro model of mast cell-mediated osteoarthritis and investigated the effect of the ethanol extract of Viscum coloratum (VEE) on IgE/antigen (IgE/Ag)-activated mast cells and mast cell-derived inflammatory mediator (MDIM)-stimulated chondrocytes. The anti-allergic effect of VEE was evaluated by degranulation, inflammatory mediators, and the FcεRI signaling cascade in IgE/Ag-activated RBL-2H3 cells. The anti-osteoarthritic action of VEE was evaluated by cell migration, and the expression, secretion, and activity of MMPs in MDIM-stimulated SW1353 cells. VEE significantly inhibited degranulation (IC50: 93.04 μg/mL), the production of IL-4 (IC50: 73.28 μg/mL), TNF-α (IC50: 50.59 μg/mL), PGD₂ and LTC₄, and activation of the FcεRI signaling cascade in IgE/Ag-activated RBL-2H3 cells. Moreover, VEE not only reduced cell migration but also inhibited the expression, secretion, and/or activity of MMP-1, MMP-3, or MMP-13 in MDIM-stimulated SW1353 cells. In conclusion, VEE possesses both anti-allergic and anti-osteoarthritic properties. Therefore, VEE could possibly be considered a new herbal drug for anti-allergic and anti-osteoarthritic therapy. Moreover, the in vitro model may be useful for the development of anti-osteoarthritic drugs.

Keywords: Viscum coloratum extract; chondrocyte; mast cell-derived inflammatory mediator; mast cells; matrix metalloprotease.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Cell Degranulation / drug effects
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Survival / drug effects
  • Chondrocytes / drug effects*
  • Chondrocytes / immunology*
  • Humans
  • Immunoglobulin E / immunology
  • Inflammation Mediators / metabolism
  • Mast Cells / drug effects*
  • Mast Cells / immunology*
  • Matrix Metalloproteinase 1 / immunology
  • Matrix Metalloproteinase 13 / immunology
  • Matrix Metalloproteinase 3 / immunology
  • Osteoarthritis / drug therapy*
  • Osteoarthritis / pathology
  • Plant Extracts / pharmacology*
  • Rats
  • Receptors, IgE / immunology
  • Signal Transduction / immunology
  • Tumor Necrosis Factor-alpha / metabolism
  • Viscum / chemistry*

Substances

  • Anti-Inflammatory Agents
  • FCER1A protein, rat
  • Inflammation Mediators
  • Plant Extracts
  • Receptors, IgE
  • Tumor Necrosis Factor-alpha
  • Immunoglobulin E
  • MMP13 protein, human
  • Matrix Metalloproteinase 13
  • MMP3 protein, human
  • Matrix Metalloproteinase 3
  • MMP1 protein, human
  • Matrix Metalloproteinase 1