TRAIL induces neutrophil apoptosis and dampens sepsis-induced organ injury in murine colon ascendens stent peritonitis

PLoS One. 2014 Jun 2;9(6):e97451. doi: 10.1371/journal.pone.0097451. eCollection 2014.

Abstract

TNF-related apoptosis inducing ligand (TRAIL) influences several inflammatory reactions by partially still unknown mechanisms. TRAIL is produced and expressed by several cells of the immune system. Murine Colon Ascendens Stent Peritonitis (CASP) represents a hyperinflammatory model of diffuse peritonitis. As we have shown previously, TRAIL strongly improves survival in murine CASP. This is accompanied by a significantly reduced infiltration of neutrophils in the associated lymphoid tissue. Additionally, it is known that TRAIL induces apoptosis in neutrophils and acceleration of neutrophil apoptosis enhances resolution of inflammatory reactions. In this study, we investigated the correlation of the protective effect of TRAIL in sepsis and its influence on neutrophils. We found that neutrophils infiltrating the lymphoid organs express the TRAIL-receptor DR5 at high density. Furthermore, we demonstrated that TRAIL-treatment enhances apoptosis of neutrophils in the spleen, lung and liver and decreases organ injury during sepsis. To further examine a role for neutrophils in TRAIL-mediated protection in CASP, we have depleted neutrophils 24 hours prior to CASP. In these depleted mice, administration of TRAIL was ineffective. We conclude that TRAIL induces apoptosis in tissue-infiltrating neutrophils thereby protecting organs from sepsis-induced injury.

MeSH terms

  • Alanine Transaminase / metabolism
  • Animals
  • Apoptosis / drug effects*
  • Aspartate Aminotransferases / metabolism
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cell Survival / drug effects
  • Colon / drug effects
  • Colon / pathology*
  • Disease Models, Animal
  • Female
  • Lipopolysaccharides
  • Mice, Inbred C57BL
  • Neutrophils / drug effects
  • Neutrophils / metabolism
  • Neutrophils / pathology*
  • Organ Specificity / drug effects*
  • Peritonitis / complications
  • Peritonitis / pathology*
  • Receptors, TNF-Related Apoptosis-Inducing Ligand / metabolism
  • Sepsis / complications
  • Sepsis / pathology*
  • Spleen / pathology
  • Stents / adverse effects
  • Survival Analysis
  • TNF-Related Apoptosis-Inducing Ligand / pharmacology*

Substances

  • Lipopolysaccharides
  • Receptors, TNF-Related Apoptosis-Inducing Ligand
  • TNF-Related Apoptosis-Inducing Ligand
  • Aspartate Aminotransferases
  • Alanine Transaminase

Grants and funding

The authors have no support or funding to report.