Cytokine and matrix metalloproteinase expression in fibroblasts from peri-implantitis lesions in response to viable Porphyromonas gingivalis

J Periodontal Res. 2013 Oct;48(5):647-56. doi: 10.1111/jre.12051. Epub 2013 Feb 27.

Abstract

Background and objective: To assess inflammatory reactions of fibroblasts in the pathophysiology of peri-implantitis, we compared the pro-inflammatory and matrix-degrading responses of gingival and granulation tissue fibroblasts from periodontally healthy controls, peri-implantitis, and periodontitis lesions to an in vitro challenge with Porphyromonas gingivalis.

Methods: Fibroblasts from periodontally healthy, peri-implantitis and periodontitis donors were challenged with viable P. gingivalis. The inflammatory reactions of fibroblasts were analyzed before and after 6 h P. gingivalis challenge, and 2.5 and 18 h after removal of the challenge. Gene expression and induction of pro-inflammatory mediators, and matrix metalloproteinases (MMPs) were assessed by real-time polymerase chain reaction. Protein expression was measured by enzyme-linked immunosorbent assay.

Results: Non-challenged fibroblasts from peri-implantitis and periodontitis lesions expressed higher levels of interleukin (IL)-1β, IL-8, and monocyte chemotactic protein (MCP)-1 than fibroblasts from periodontally healthy individuals. The P. gingivalis challenge induced expression of IL-1β, IL-8, IL-6, MCP-1, and MMP-1 in periodontitis and peri-implantitis fibroblasts, but not in fibroblasts from periodontally healthy individuals. MMP-8 expression was higher in non-challenged peri-implantitis fibroblasts than in fibroblasts from periodontally healthy individuals. However, the P. gingivalis challenge downregulated MMP-8 gene expression in peri-implantitis fibroblasts. After removal of the P. gingivalis challenge, peri-implantitis fibroblasts sustained higher induction of IL-1β, MCP-1, and MMP-1 compared to periodontitis fibroblasts.

Conclusions: Fibroblasts from peri-implantitis and periodontitis lesions gave a more pronounced inflammatory response to the P. gingivalis challenge than fibroblasts from healthy donors. They may therefore be involved in the development of inflammation in peri-implantitis and periodontitis. Moreover, the sustained upregulation of inflammatory mediators and MMP-1 in peri-implantitis fibroblasts may play a role in the pathogenesis of peri-implantitis.

Keywords: cytokines; dental implants; matrix metalloproteinases; periodontitis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Culture Techniques
  • Cells, Cultured
  • Chemokine CCL2 / analysis
  • Chronic Periodontitis / enzymology
  • Chronic Periodontitis / immunology
  • Chronic Periodontitis / microbiology
  • Cytokines / analysis*
  • Female
  • Fibroblasts / enzymology
  • Fibroblasts / immunology
  • Fibroblasts / microbiology
  • Gingiva / enzymology
  • Gingiva / immunology
  • Gingiva / microbiology*
  • Granulation Tissue / enzymology
  • Granulation Tissue / immunology
  • Granulation Tissue / microbiology
  • Humans
  • Inflammation Mediators / analysis
  • Interleukin-1beta / analysis
  • Interleukin-6 / analysis
  • Interleukin-8 / analysis
  • Male
  • Matrix Metalloproteinase 1 / analysis
  • Matrix Metalloproteinase 8 / analysis
  • Matrix Metalloproteinases / analysis*
  • Middle Aged
  • Peri-Implantitis / enzymology
  • Peri-Implantitis / immunology
  • Peri-Implantitis / microbiology*
  • Porphyromonas gingivalis / enzymology
  • Porphyromonas gingivalis / immunology*
  • Real-Time Polymerase Chain Reaction
  • Time Factors
  • Up-Regulation

Substances

  • CCL2 protein, human
  • CXCL8 protein, human
  • Chemokine CCL2
  • Cytokines
  • IL6 protein, human
  • Inflammation Mediators
  • Interleukin-1beta
  • Interleukin-6
  • Interleukin-8
  • Matrix Metalloproteinases
  • MMP8 protein, human
  • Matrix Metalloproteinase 8
  • MMP1 protein, human
  • Matrix Metalloproteinase 1