Mechanisms of IL-8 suppression by Treponema denticola in gingival epithelial cells

Immunol Cell Biol. 2014 Feb;92(2):139-47. doi: 10.1038/icb.2013.80. Epub 2013 Dec 3.

Abstract

The purpose of this study was to investigate the mechanism(s) of interleukin (IL)-8 suppression by Treponema denticola, one of the major periodontal pathogens, in gingival epithelial cells. Immortalized human gingival epithelial HOK-16B cells were infected with wild-type (WT), dentilisin-deficient (K1) or flagellin-deficient (flgE) T. denticola in the presence or absence of 2% human serum for 24 h. The levels of IL-8 expression were measured with real-time reverse transcription PCR and ELISA. In the absence of human serum, the WT and flgE, but not K1, substantially reduced not only the levels of IL-8 protein but also of IL-8 mRNA. Such downregulation of IL-8 mRNA was independent of bacterial invasion. Degradation of cytokine mixture by the WT, K1 and flgE revealed dentilisin-dependent preferential degradation of tumor necrosis factor (TNF)-α, an IL-8-inducing cytokine. WT and flgE significantly decreased the levels of TNFα secreted by HOK-16B cells, suggesting modulation of IL-8 through dentilisin-mediated degradation of TNFα. The addition of human serum to the culture potentiated the suppressive effect of T. denticola, resulting in substantial reductions of IL-8 and TNFα levels, even by K1. The serum-dependent effects of T. denticola were attributed to its ability to suppress the accumulation of intracellular reactive-oxygen species (ROS), a group of ubiquitous signaling molecules. Pretreatment with an antioxidant suppressed TNFα-induced IL-8 expression, confirming the role of ROS in TNFα signaling. Collectively, T. denticola targeted a key inflammatory cytokine and its signaling molecule to modulate the host innate immune response, which provides a new insight into modulation of host immunity by a periodontal pathogen.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / immunology
  • Bacterial Proteins / metabolism
  • Cell Line
  • Chymotrypsin / genetics
  • Chymotrypsin / immunology
  • Chymotrypsin / metabolism
  • Gene Expression Regulation / immunology*
  • Gingiva / immunology*
  • Gingiva / metabolism
  • Gingiva / microbiology
  • Gingiva / pathology
  • Humans
  • Inflammation / genetics
  • Inflammation / immunology
  • Inflammation / metabolism
  • Inflammation / microbiology
  • Inflammation / pathology
  • Interleukin-8 / biosynthesis
  • Interleukin-8 / genetics
  • Interleukin-8 / immunology*
  • Keratinocytes / immunology*
  • Keratinocytes / metabolism
  • Keratinocytes / pathology
  • Peptide Hydrolases
  • Proteolysis
  • Reactive Oxygen Species / immunology
  • Reactive Oxygen Species / metabolism
  • Treponema denticola / genetics
  • Treponema denticola / immunology*
  • Treponema denticola / metabolism
  • Treponemal Infections / genetics
  • Treponemal Infections / immunology*
  • Treponemal Infections / metabolism
  • Treponemal Infections / pathology
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Bacterial Proteins
  • CXCL8 protein, human
  • FlgE protein, Bacteria
  • Interleukin-8
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • Peptide Hydrolases
  • dentilisin
  • Chymotrypsin