Substance P enhances expression of lipopolysaccharide-induced inflammatory factors in dental pulp cells

J Endod. 2004 Nov;30(11):770-3. doi: 10.1097/00004770-200411000-00005.

Abstract

To examine how substance P (SP) is related with dental pulp inflammation, we examined the effects of SP on expression of genes for inflammatory factors in human dental pulp cell cultures. Using reverse transcriptase-polymerase chain reaction, we found that Prevotella intermedia lipopolysaccharide (LPS) induced expression of SP and SP-receptor mRNAs, and that somatostatin inhibited the LPS-induced expression of SP mRNA. We also found that SP enhanced LPS-induced stimulation of NF-kappaB binding activity. In addition, SP induced expression of cyclooxygenase-2 and interleukin-10 receptor mRNAs. In contrast, SP inhibited expression of interferon-gamma receptor mRNA. These results suggest that SP may play a regulatory role in the immunological response of dental pulp tissue to pathogenic bacteria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autocrine Communication
  • Blotting, Western
  • Cells, Cultured
  • Cyclooxygenase 2
  • Dental Pulp / cytology
  • Dental Pulp / immunology*
  • Dental Pulp / metabolism*
  • Fibroblasts / metabolism
  • Gene Expression
  • Humans
  • Inflammation Mediators / metabolism*
  • Interferon gamma Receptor
  • Isoenzymes / biosynthesis
  • Isoenzymes / genetics
  • Lipopolysaccharides / pharmacology*
  • Membrane Proteins
  • NF-kappa B / metabolism
  • Prevotella intermedia / chemistry
  • Prostaglandin-Endoperoxide Synthases / biosynthesis
  • Prostaglandin-Endoperoxide Synthases / genetics
  • RNA, Messenger / analysis
  • Receptors, Interferon / antagonists & inhibitors
  • Receptors, Interleukin / biosynthesis
  • Receptors, Interleukin-10
  • Receptors, Neurokinin-1 / biosynthesis
  • Receptors, Neurokinin-1 / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Substance P / biosynthesis
  • Substance P / genetics
  • Substance P / physiology*
  • Up-Regulation

Substances

  • Inflammation Mediators
  • Isoenzymes
  • Lipopolysaccharides
  • Membrane Proteins
  • NF-kappa B
  • RNA, Messenger
  • Receptors, Interferon
  • Receptors, Interleukin
  • Receptors, Interleukin-10
  • Receptors, Neurokinin-1
  • Substance P
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases