Angiogenic signaling triggered by cariogenic bacteria in pulp cells

J Dent Res. 2009 Sep;88(9):835-40. doi: 10.1177/0022034509341946.

Abstract

The inflammation observed in the dental pulp of teeth with deep caries lesions is characterized by a significant increase in blood vessel density. It is known that lipoteichoic acid (LTA) from Gram-positive cariogenic bacteria induces expression of vascular endothelial growth factor (VEGF) in dental pulp cells. The hypothesis underlying this study was that LTA induces VEGF expression in dental pulp cells through TLR2 and PI3k/Akt signaling. Odontoblast-like cells (MDPC-23) and undifferentiated pulp cells (OD-21) were exposed to LTA from Streptococcus sanguis, and the role of TLR2, PI3K/Akt, and IKK signaling in LTA-induced VEGF expression was evaluated. These studies demonstrated that TLR2 signaling through the PI3K-Akt pathway is necessary for LTA-induced VEGF expression in pulp cells. In contrast, inhibition of IKK signaling did not prevent VEGF up-regulation in response to LTA. Understanding signaling pathways triggered by cariogenic bacteria may reveal novel therapeutic targets for the clinical management of pulpitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Dental Caries / microbiology*
  • Dental Pulp / blood supply
  • Dental Pulp / cytology
  • Dental Pulp / microbiology*
  • Fibroblasts / drug effects
  • Gingiva / cytology
  • Gingiva / drug effects
  • I-kappa B Kinase / analysis
  • I-kappa B Kinase / drug effects
  • Lipopolysaccharides / pharmacology
  • Macrophages / drug effects
  • Mice
  • Microvessels / drug effects
  • Microvessels / pathology
  • Neovascularization, Physiologic / physiology*
  • Odontoblasts / drug effects
  • Phosphatidylinositol 3-Kinases / analysis
  • Phosphatidylinositol 3-Kinases / drug effects
  • Proto-Oncogene Proteins c-akt / analysis
  • Proto-Oncogene Proteins c-akt / drug effects
  • Pulpitis / microbiology
  • Pulpitis / pathology
  • Signal Transduction / physiology*
  • Streptococcus sanguis / physiology*
  • Teichoic Acids / pharmacology
  • Toll-Like Receptor 2 / analysis
  • Toll-Like Receptor 2 / drug effects
  • Up-Regulation
  • Vascular Endothelial Growth Factor A / analysis
  • Vascular Endothelial Growth Factor A / drug effects
  • Vascular Endothelial Growth Factor Receptor-2 / analysis
  • Vascular Endothelial Growth Factor Receptor-2 / drug effects

Substances

  • Lipopolysaccharides
  • Teichoic Acids
  • Tlr2 protein, mouse
  • Toll-Like Receptor 2
  • Vascular Endothelial Growth Factor A
  • vascular endothelial growth factor A, mouse
  • lipoteichoic acid
  • Vascular Endothelial Growth Factor Receptor-2
  • Proto-Oncogene Proteins c-akt
  • I-kappa B Kinase
  • Ikbkb protein, mouse