Role of the lipoxin A4 receptor in the development of neutrophil extracellular traps in Leishmania infantum infection

Parasit Vectors. 2019 May 29;12(1):275. doi: 10.1186/s13071-019-3530-8.

Abstract

Background: Neutrophils play an immunomodulatory role through the release of neutrophil extracellular traps (NETs). NETs are released in response to Leishmania infection, but the mechanism of NET extrusion has not been elucidated. The lipoxin A4 receptor on neutrophils is crucial for the inflammatory response and immune regulation of many diseases, including Leishmania infection. Therefore, in the present study, we tried to explore whether Leishmania infantum promastigotes stimulate neutrophil activation and NET release via activating the lipoxin A4 receptor.

Results: Leishmania infantum promastigotes stimulated neutrophil activity, but blocking of the lipoxin A4 receptor with its antagonist Boc prior to L. infantum stimulation abrogated these effects. Neutrophils showed citrullinated histone H3 expression and simultaneous NET extrusion on L. infantum stimulation, but a decline in both was observed on blocking of the lipoxin A4 receptor. Moreover, differentiated HL-60 cells with lipoxin A4 receptor silencing showed a decrease in citrullinated histone H3 expression as compared to the unsilenced HL-60 samples on stimulation with promastigotes.

Conclusions: Leishmania infantum promastigotes altered the characteristics of neutrophils and induced NET extrusion by activating the lipoxin A4 receptor. The lipoxin A4 receptor may have potential as a therapeutic target in relation to NET extrusion in the treatment of leishmaniasis, but its mechanisms of action need to be explored in more depth.

Keywords: Citrullinated histone H3; Leishmania infantum; Lipoxin A4 receptor; Neutrophil extracellular traps.

MeSH terms

  • Animals
  • Citrullination
  • Extracellular Traps / immunology*
  • Female
  • Gene Silencing
  • HL-60 Cells
  • Histones / metabolism
  • Humans
  • Leishmania infantum / immunology*
  • Lipoxins / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • Neutrophils / immunology*
  • Neutrophils / parasitology
  • Receptors, Formyl Peptide / antagonists & inhibitors
  • Receptors, Formyl Peptide / immunology*
  • Receptors, Lipoxin / antagonists & inhibitors
  • Receptors, Lipoxin / immunology*

Substances

  • FPR2 protein, human
  • Histones
  • Lipoxins
  • Receptors, Formyl Peptide
  • Receptors, Lipoxin
  • lipoxin A4