Phospholipase C, p38/MAPK, and NF-kappaB-mediated induction of MIP-3alpha/CCL20 by Porphyromonas gingivalis

Innate Immun. 2010 Aug;16(4):226-34. doi: 10.1177/1753425909339237. Epub 2009 Aug 26.

Abstract

Macrophage inflammatory protein-3alpha/C-C chemokine ligand 20 (MIP-3alpha/CCL20) is an antimicrobial peptide that plays an important role in innate immunity. In addition to direct microbicidal effects, MIP-3alpha/CCL20 also exhibits cytokine-like functions that are critical during dendritic cell activation. The aim of the present study was to investigate further which signaling pathways are involved in the MIP-3alpha/CCL20 mRNA expression in response to whole-cell Porphyromonas gingivalis. Primary gingival epithelial cells (GECs) and the immortalized oral keratinocyte cell-line OKF6/TERT-2 were stimulated with whole-cell P. gingivalis. Prior to stimulation, GECs and OKF6/TERT-2 cells were pretreated with specific inhibitors for nuclear-factor-kappaB (NF-kappaB), mitogen-activated protein kinase (MAPK), phospholipase C (PLC), and phosphatidylinositol-3-kinase (PI3K). In GECs and OKF6/TERT-2 cells, activation of NF-kappaB was examined after exposure to P. gingivalis. The gene expression of MIP-3alpha/CCL20 was significantly induced in response to P. gingivalis (P <or= 0.05) compared to unstimulated control cells. This induction was specifically blocked when cells were pre-incubated with inhibitors for NF-kappaB, MAPK, and PLC (P <or= 0.05), but not for PI3K. These results demonstrate that P. gingivalis induces the MIP-3alpha/CCL20 mRNA in a NF-kappaB-, PLC-, and MAPK-dependent manner.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Chemokine CCL20 / biosynthesis*
  • Chemokine CCL20 / genetics
  • Epithelial Cells / physiology
  • Gingiva / cytology
  • Humans
  • Indicators and Reagents
  • Interleukin-6 / biosynthesis
  • Interleukin-6 / genetics
  • NF-kappa B / physiology*
  • NFATC Transcription Factors / physiology
  • Phosphatidylinositol 3-Kinases / physiology
  • Porphyromonas gingivalis / metabolism*
  • RNA / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factor RelA / biosynthesis
  • Transcription Factor RelA / genetics
  • Transcription Factor RelA / physiology
  • Transfection
  • Type C Phospholipases / physiology*
  • p38 Mitogen-Activated Protein Kinases / physiology*

Substances

  • CCL20 protein, human
  • Chemokine CCL20
  • Indicators and Reagents
  • Interleukin-6
  • NF-kappa B
  • NFATC Transcription Factors
  • Transcription Factor RelA
  • RNA
  • Phosphatidylinositol 3-Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Type C Phospholipases