Activated protein C inhibits neutrophil extracellular trap formation in vitro and activation in vivo

J Biol Chem. 2017 May 26;292(21):8616-8629. doi: 10.1074/jbc.M116.768309. Epub 2017 Apr 13.

Abstract

Activated protein C (APC) is a multifunctional serine protease with anticoagulant, cytoprotective, and anti-inflammatory activities. In addition to the cytoprotective effects of APC on endothelial cells, podocytes, and neurons, APC cleaves and detoxifies extracellular histones, a major component of neutrophil extracellular traps (NETs). NETs promote pathogen clearance but also can lead to thrombosis; the pathways that negatively regulate NETosis are largely unknown. Thus, we studied whether APC is capable of directly inhibiting NETosis via receptor-mediated cell signaling mechanisms. Here, by quantifying extracellular DNA or myeloperoxidase, we demonstrate that APC binds human leukocytes and prevents activated platelet supernatant or phorbol 12-myristate 13-acetate (PMA) from inducing NETosis. Of note, APC proteolytic activity was required for inhibiting NETosis. Moreover, antibodies against the neutrophil receptors endothelial protein C receptor (EPCR), protease-activated receptor 3 (PAR3), and macrophage-1 antigen (Mac-1) blocked APC inhibition of NETosis. Select mutations in the Gla and protease domains of recombinant APC caused a loss of NETosis. Interestingly, pretreatment of neutrophils with APC prior to induction of NETosis inhibited platelet adhesion to NETs. Lastly, in a nonhuman primate model of Escherichia coli-induced sepsis, pretreatment of animals with APC abrogated release of myeloperoxidase from neutrophils, a marker of neutrophil activation. These findings suggest that the anti-inflammatory function of APC at therapeutic concentrations may include the inhibition of NETosis in an EPCR-, PAR3-, and Mac-1-dependent manner, providing additional mechanistic insight into the diverse functions of neutrophils and APC in disease states including sepsis.

Keywords: Mac-1; PAR3; activated protein C; cell biology; cell signaling; coagulation factor; endothelial protein C receptor; hemostasis; neutrophil; neutrophil extracellular traps; protein C; thrombosis.

MeSH terms

  • Animals
  • Antigens, CD / immunology
  • Antigens, CD / metabolism
  • Disease Models, Animal
  • Endothelial Protein C Receptor
  • Escherichia coli
  • Escherichia coli Infections / blood
  • Escherichia coli Infections / immunology
  • Extracellular Traps / immunology*
  • Extracellular Traps / metabolism
  • Female
  • Humans
  • Macrophage-1 Antigen / immunology
  • Macrophage-1 Antigen / metabolism
  • Male
  • Neutrophil Activation / drug effects
  • Neutrophil Activation / immunology*
  • Neutrophils / immunology*
  • Neutrophils / metabolism
  • Papio anubis
  • Protein C / immunology*
  • Protein C / metabolism
  • Receptors, Cell Surface / immunology
  • Receptors, Cell Surface / metabolism
  • Sepsis / blood
  • Sepsis / immunology
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Antigens, CD
  • Endothelial Protein C Receptor
  • Macrophage-1 Antigen
  • PROCR protein, human
  • Protein C
  • Receptors, Cell Surface
  • Tetradecanoylphorbol Acetate