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

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 inflammator...

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Autores principales: Wei, Furong, Gong, Wenci, Wang, Junyun, Yang, Yuetao, Liu, Jianxiu, Wang, Yanjuan, Cao, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542009/
https://www.ncbi.nlm.nih.gov/pubmed/31142352
http://dx.doi.org/10.1186/s13071-019-3530-8
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author Wei, Furong
Gong, Wenci
Wang, Junyun
Yang, Yuetao
Liu, Jianxiu
Wang, Yanjuan
Cao, Jianping
author_facet Wei, Furong
Gong, Wenci
Wang, Junyun
Yang, Yuetao
Liu, Jianxiu
Wang, Yanjuan
Cao, Jianping
author_sort Wei, Furong
collection PubMed
description 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.
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spelling pubmed-65420092019-06-03 Role of the lipoxin A4 receptor in the development of neutrophil extracellular traps in Leishmania infantum infection Wei, Furong Gong, Wenci Wang, Junyun Yang, Yuetao Liu, Jianxiu Wang, Yanjuan Cao, Jianping Parasit Vectors Research 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. BioMed Central 2019-05-29 /pmc/articles/PMC6542009/ /pubmed/31142352 http://dx.doi.org/10.1186/s13071-019-3530-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wei, Furong
Gong, Wenci
Wang, Junyun
Yang, Yuetao
Liu, Jianxiu
Wang, Yanjuan
Cao, Jianping
Role of the lipoxin A4 receptor in the development of neutrophil extracellular traps in Leishmania infantum infection
title Role of the lipoxin A4 receptor in the development of neutrophil extracellular traps in Leishmania infantum infection
title_full Role of the lipoxin A4 receptor in the development of neutrophil extracellular traps in Leishmania infantum infection
title_fullStr Role of the lipoxin A4 receptor in the development of neutrophil extracellular traps in Leishmania infantum infection
title_full_unstemmed Role of the lipoxin A4 receptor in the development of neutrophil extracellular traps in Leishmania infantum infection
title_short Role of the lipoxin A4 receptor in the development of neutrophil extracellular traps in Leishmania infantum infection
title_sort role of the lipoxin a4 receptor in the development of neutrophil extracellular traps in leishmania infantum infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542009/
https://www.ncbi.nlm.nih.gov/pubmed/31142352
http://dx.doi.org/10.1186/s13071-019-3530-8
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