Arginine-specific gingipain A from Porphyromonas gingivalis induces Weibel-Palade body exocytosis and enhanced activation of vascular endothelial cells through protease-activated receptors

Microbes Infect. 2007 Oct;9(12-13):1500-6. doi: 10.1016/j.micinf.2007.08.005. Epub 2007 Aug 23.

Abstract

Gingipains, cysteine proteases derived from Porphyromonas gingivalis, are important virulence factors in periodontal diseases. We found that arginine-specific gingipain A (RgpA) increased the responsiveness of vascular endothelial cells to P. gingivalis lipopolysaccharides (LPS) and P. gingivalis whole cells to induce enhanced IL-8 production through protease-activated receptors (PARs) and phospholipase C (PLC) gamma. We therefore investigated whether RgpA-induced enhanced cell activation is mediated through exocytosis of Weibel-Palade bodies (WPBs) because they store vasoactive substances. RgpA rapidly activated PAR- and PLCgamma-dependent WPB exocytosis. In addition, angiopoietin (Ang)-2, a substance of WPB, enhanced IL-8 production by P. gingivalis LPS, suggesting that Ang-2 mediates the RgpA-induced enhanced cell responses. Thus, we propose a novel role for RgpA in induction of a proinflammatory event through PAR-mediated WPB exocytosis, which may be an important step for enhanced endothelial responses to P. gingivalis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adhesins, Bacterial / immunology*
  • Cells, Cultured
  • Cysteine Endopeptidases / immunology*
  • Endothelial Cells / immunology*
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / immunology*
  • Exocytosis / physiology*
  • Gingipain Cysteine Endopeptidases
  • Humans
  • Porphyromonas gingivalis / immunology*
  • Receptors, Proteinase-Activated / metabolism*
  • Umbilical Veins
  • Weibel-Palade Bodies / physiology*

Substances

  • Adhesins, Bacterial
  • Gingipain Cysteine Endopeptidases
  • Receptors, Proteinase-Activated
  • Cysteine Endopeptidases