Micronutrient modulation of NF-κB in oral keratinocytes exposed to periodontal bacteria

Innate Immun. 2013;19(2):140-51. doi: 10.1177/1753425912454761. Epub 2012 Aug 13.

Abstract

Chronic periodontal diseases are characterised by a dysregulated and exaggerated inflammatory/immune response to plaque bacteria. We have demonstrated previously that oral keratinocytes up-regulate key molecular markers of inflammation, including NF-κB and cytokine signalling, when exposed to the periodontal bacteria Porphyromonas gingivalis and Fusobacterium nucleatum in vitro. The purpose of the current study was to investigate whether α-lipoic acid was able to abrogate bacterially-induced pro-inflammatory changes in the H400 oral epithelial cell line. Initial studies indicated that α-lipoic acid supplementation (1-4 mM) significantly reduced cell attachment; lower concentrations (<0.5 mM) enabled >85% cell adhesion at 24 h. While a pro-inflammatory response, demonstrable by NF-κB translocation, gene expression and protein production was evident in H400 cells following exposure to P. gingivalis and F. nucleatum, pre-incubation of cells with 0.5 mM α-lipoic acid modulated this response. α-Lipoic acid pre-treatment significantly decreased levels of bacterially-induced NF-κB activation and IL-8 protein production, and differentially modulated transcript levels for IL-8, IL-1β, TNF-α and GM-CSF, TLR2, 4, 9, S100A8, S100A9, lysyl oxidase, NF-κB1, HMOX, and SOD2. Overall, the data indicate that α-lipoic acid exerts an anti-inflammatory effect on oral epithelial cells exposed to periodontal bacteria and thus may provide a novel adjunctive treatment for periodontal diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteroidaceae Infections / drug therapy
  • Bacteroidaceae Infections / immunology*
  • Cell Line
  • Fusobacterium Infections / drug therapy
  • Fusobacterium Infections / immunology*
  • Fusobacterium nucleatum / immunology*
  • Humans
  • Inflammation Mediators / metabolism
  • Interleukin-8 / metabolism
  • Keratinocytes / drug effects
  • Keratinocytes / immunology*
  • Keratinocytes / microbiology
  • Mouth / immunology
  • Mouth / pathology
  • NF-kappa B / metabolism*
  • Porphyromonas gingivalis / immunology*
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • Thioctic Acid / pharmacology
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcriptional Activation / drug effects
  • Transcriptional Activation / immunology

Substances

  • Inflammation Mediators
  • Interleukin-8
  • NF-kappa B
  • Transcription Factors
  • Thioctic Acid