Epithelial cell-derived human beta-defensin-2 acts as a chemotaxin for mast cells through a pertussis toxin-sensitive and phospholipase C-dependent pathway

Int Immunol. 2002 Apr;14(4):421-6. doi: 10.1093/intimm/14.4.421.

Abstract

Mast cells are known to accumulate at the sites of inflammation in response to chemoattractants generated in the local milieu. Since human beta-defensin-2 (hBD-2) is generated in several epithelial tissues where mast cells are present and because we have recently reported that this human antibacterial peptide induces mast cell degranulation, we thus hypothesized that hBD-2 could be a mast cell chemotaxin. Here we report that hBD-2 directly and specifically induces mast cell migration with an optimal concentration of 3 microg/ml. Checkerboard analysis showed that the migration was more chemotactic rather than chemokinetic. Moreover, Scatchard analysis using 125I-labeled hBD-2 revealed that mast cells have at least two classes of receptors, high- and low-affinity receptors, for this peptide. Moreover, the competitive binding assay suggested that hBD-2 is unlikely to utilize CCR6, a functional receptor for hBD-2-mediated dendritic and T cell migration, on mast cells. In addition, treatment of mast cells with G protein inhibitor, pertussis toxin, and phospholipase C inhibitor, U-73122, abolished the cell chemotaxis in response to hBD-2, indicating that the G protein-phospholipase C signaling pathway is involved in hBD-2-induced mast cell activation. Thus, we suggest that hBD-2, which was originally believed to be involved in innate host defense, may participate in the recruitment of mast cells to inflammation foci.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Movement / drug effects
  • Chemotactic Factors / pharmacology
  • Chemotaxis / drug effects
  • Epithelium / metabolism*
  • Estrenes / antagonists & inhibitors
  • Humans
  • Mast Cells / drug effects*
  • Pertussis Toxin
  • Pyrrolidinones / antagonists & inhibitors
  • Rats
  • Signal Transduction / physiology
  • Type C Phospholipases / metabolism*
  • Virulence Factors, Bordetella / pharmacology
  • beta-Defensins / pharmacology
  • beta-Defensins / physiology*

Substances

  • Chemotactic Factors
  • DEFB4A protein, human
  • Estrenes
  • Pyrrolidinones
  • Virulence Factors, Bordetella
  • beta-Defensins
  • 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione
  • Pertussis Toxin
  • Type C Phospholipases