Matrix metalloproteinases regulate extracellular levels of SDF-1/CXCL12, IL-6 and VEGF in hydrogen peroxide-stimulated human periodontal ligament fibroblasts

Cytokine. 2015 May;73(1):114-21. doi: 10.1016/j.cyto.2015.02.001. Epub 2015 Mar 6.

Abstract

Periodontitis is a highly prevalent infectious disease characterized by the progressive inflammatory destruction of tooth-supporting structures, leading to tooth loss. The underling molecular mechanisms of the disease are incompletely understood, precluding the development of more efficient screening, diagnostic and therapeutic approaches. We investigated the interrelation of three known effector mechanisms of the cellular response to periodontal infection, namely reactive oxygen species (ROS), matrix metalloproteinases (MMPs) and cytokines in primary cell cultures of human periodontal ligament fibroblast (hPDLF). We demonstrated that ROS increase the activity/levels of gelatinolytic MMPs, and stimulate cytokine secretion in hPDLF. Additionally, we proved that MMPs possesses immune modulatory capacity, regulating the secreted levels of cytokines in ROS-stimulated hPDLF cultures. This evidence provides further insight in the molecular pathogenesis of periodontitis, contributing to the future development of more effective therapies.

Keywords: Cytokines; Matrix metalloproteinases; Oxidative stress; Periodontal ligament fibroblast.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antioxidants / metabolism
  • Cell Movement / drug effects
  • Chemokine CXCL12 / metabolism*
  • Extracellular Space / drug effects
  • Extracellular Space / metabolism
  • Female
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Fibroblasts / enzymology*
  • Gelatin / metabolism
  • Humans
  • Hydrogen Peroxide / pharmacology*
  • Hydroxamic Acids
  • Indoles / pharmacology
  • Interleukin-6 / metabolism*
  • Male
  • Matrix Metalloproteinases / metabolism*
  • Periodontal Ligament / cytology*
  • Solubility
  • Vascular Endothelial Growth Factor A / metabolism*

Substances

  • Antioxidants
  • CXCL12 protein, human
  • Chemokine CXCL12
  • Hydroxamic Acids
  • IL6 protein, human
  • Indoles
  • Interleukin-6
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • Gelatin
  • Hydrogen Peroxide
  • Matrix Metalloproteinases
  • ilomastat