N-acetylated Proline-Glycine-Proline induced G-protein dependent chemotaxis of neutrophils is independent of CXCL8 release

Eur J Pharmacol. 2011 Oct 15;668(3):428-34. doi: 10.1016/j.ejphar.2011.03.022. Epub 2011 Mar 31.

Abstract

Chronic inflammation in lung diseases contributes to lung tissue destruction leading to the formation of chemotactic collagen fragments such as N-acetylated Proline-Glycine-Proline (N-ac-PGP). In this study, we investigated in more detail the mechanism of action of N-ac-PGP in neutrophilic inflammation. N-ac-PGP was chemotactic for human neutrophils via pertussis toxin sensitive G protein-coupled receptors in vitro and directly activated this cell type, which led to cytosolic calcium mobilization and release of CXCL8. Furthermore, using a selective CXCR2 antagonist confirmed that N-ac-PGP-induced neutrophil chemotaxis is mediated through CXCR2 activation. To determine whether N-ac-PGP was solely responsible for the migration and activation of human neutrophils in vitro and not the released CXCL8 upon stimulation with N-ac-PGP, an antibody directed against CXCL8 was used. Performing chemotaxis and calcium influx assays in the presence of this antibody did not alter the effects of N-ac-PGP whereas effects of CXCL8 were attenuated. These experiments indicate that N-ac-PGP, in addition to the direct induction of chemotaxis, also directly activates neutrophils to release CXCL8. In vivo, this may lead in the long term to a self-maintaining situation enhanced by both N-ac-PGP and CXCL8, leading to a further increase in neutrophil infiltration and chronic inflammation.

MeSH terms

  • Antibodies / immunology
  • Calcium / metabolism
  • Chemotaxis, Leukocyte / drug effects*
  • Collagen / metabolism
  • Heterotrimeric GTP-Binding Proteins / metabolism*
  • Humans
  • Imidazoles / chemistry
  • Imidazoles / pharmacology
  • Interleukin-8 / antagonists & inhibitors
  • Interleukin-8 / immunology
  • Interleukin-8 / metabolism*
  • Neutrophils / cytology*
  • Neutrophils / drug effects*
  • Neutrophils / metabolism
  • Oligopeptides / pharmacology*
  • Peptide Fragments / pharmacology
  • Pertussis Toxin / toxicity
  • Receptors, G-Protein-Coupled / metabolism
  • Receptors, Interleukin-8B / metabolism

Substances

  • Antibodies
  • Imidazoles
  • Interleukin-8
  • N-acetyl-proline-glycine-proline
  • Oligopeptides
  • Peptide Fragments
  • Receptors, G-Protein-Coupled
  • Receptors, Interleukin-8B
  • Collagen
  • Pertussis Toxin
  • Heterotrimeric GTP-Binding Proteins
  • Calcium