Effect of proinflammatory cytokines on the expression and regulation of human beta-defensin 2 in human dental pulp cells

J Endod. 2010 Jan;36(1):64-9. doi: 10.1016/j.joen.2009.09.022.

Abstract

Introduction: Although the expression of human beta-defensin-2 (hBD-2) in odontoblasts from human dental pulp (HDP) has been reported, the production of hBD-2 and its regulation remains poorly understood. The aim of this study was to investigate the effect of cytokines on the induction of hBD-2 and its signaling mechanisms in HDP cells.

Methods: After stimulation with tumor necrosis factor alpha (TNF-alpha) and interleukin 1 alpha (IL-1 alpha), reverse-transcriptase polymerase chain reaction, Western blot, and enzyme-linked immunosorbent assay experiments were performed to evaluate the effects of these cytokines on the production of hBD-2.

Results: TNF-alpha and IL-1 alpha synergistically increased hBD-2 messenger RNA levels, protein expression, and activity. The up-regulation of hBD-2 by cytokines was attenuated by pretreatment with inhibitors of PKC, JNK, p38, ERK MAPK, nuclear factor-kappaB, and adenosine monophosphate-activated protein kinase (AMPK).

Conclusion: These results suggest that TNF-alpha and IL-1 alpha up-regulate HBD-2 expression in HDP cells through the PKC, JNK MAPK, p38, ERK, NF-kappaB, and AMPK pathways. Thus, the induction of hBD-2 by proinflammatory cytokines might up-regulate the pulpal host immune defense system.

MeSH terms

  • AMP-Activated Protein Kinases / antagonists & inhibitors
  • AMP-Activated Protein Kinases / metabolism
  • Cell Line, Transformed
  • Cytokines / physiology*
  • Dental Pulp / cytology
  • Dental Pulp / drug effects
  • Dental Pulp / immunology*
  • Dental Pulp / metabolism*
  • Gene Expression
  • Gene Knockdown Techniques
  • Humans
  • Inflammation Mediators / pharmacology*
  • Interleukin-1alpha / pharmacology
  • Interleukin-1alpha / physiology
  • MAP Kinase Signaling System
  • NF-kappa B / antagonists & inhibitors
  • NF-kappa B / metabolism
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / metabolism
  • Recombinant Proteins / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / pharmacology
  • Tumor Necrosis Factor-alpha / physiology
  • Up-Regulation
  • beta-Defensins / genetics
  • beta-Defensins / metabolism*

Substances

  • Cytokines
  • DEFB4A protein, human
  • Inflammation Mediators
  • Interleukin-1alpha
  • NF-kappa B
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • beta-Defensins
  • Protein Kinase C
  • AMP-Activated Protein Kinases