Priming of Human Neutrophils Is Necessary for Their Activation by Extracellular DNA

Biochemistry (Mosc). 2016 Jun;81(6):609-14. doi: 10.1134/S0006297916060079.

Abstract

Extracellular plasma DNA is thought to act as a damage-associated molecular pattern causing activation of immune cells. However, purified preparations of mitochondrial and nuclear DNA were unable to induce neutrophil activation in vitro. Thus, we examined whether granulocyte-macrophage colony-stimulating factor (GM-CSF) acting as a neutrophil priming agent can promote the activation of neutrophils by different types of extracellular DNA. GM-CSF pretreatment greatly increased p38 MAPK phosphorylation and promoted CD11b/CD66b expression in human neutrophils treated with mitochondrial and, to a lesser extent, with nuclear DNA. Our experiments clearly indicate that GM-CSF-induced priming of human neutrophils is necessary for their subsequent activation by extracellular DNA.

MeSH terms

  • Antigens, CD / metabolism
  • CD11b Antigen / metabolism
  • Cell Adhesion Molecules / metabolism
  • Cells, Cultured
  • DNA / pharmacology*
  • DNA, Mitochondrial / pharmacology
  • GPI-Linked Proteins / metabolism
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Humans
  • Neutrophil Activation / drug effects*
  • Neutrophils / cytology
  • Neutrophils / drug effects
  • Neutrophils / metabolism*
  • Phosphorylation / drug effects
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Antigens, CD
  • CD11b Antigen
  • CEACAM8 protein, human
  • Cell Adhesion Molecules
  • DNA, Mitochondrial
  • GPI-Linked Proteins
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • DNA
  • p38 Mitogen-Activated Protein Kinases