Cargando…

CXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis

Sepsis is a life-threatening organ dysfunction condition caused by a dysregulated host response to an infection. Here we report that the circulating levels of growth and differentiation factor-15 (GDF15) are strongly increased in septic shock patients and correlate with mortality. In mice, we find t...

Descripción completa

Detalles Bibliográficos
Autores principales: Santos, Isa, Colaço, Henrique G., Neves-Costa, Ana, Seixas, Elsa, Velho, Tiago R., Pedroso, Dora, Barros, André, Martins, Rui, Carvalho, Nuno, Payen, Didier, Weis, Sebastian, Yi, Hyon-Seung, Shong, Minho, Moita, Luís F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275717/
https://www.ncbi.nlm.nih.gov/pubmed/32424099
http://dx.doi.org/10.1073/pnas.1918508117
_version_ 1783542841540083712
author Santos, Isa
Colaço, Henrique G.
Neves-Costa, Ana
Seixas, Elsa
Velho, Tiago R.
Pedroso, Dora
Barros, André
Martins, Rui
Carvalho, Nuno
Payen, Didier
Weis, Sebastian
Yi, Hyon-Seung
Shong, Minho
Moita, Luís F.
author_facet Santos, Isa
Colaço, Henrique G.
Neves-Costa, Ana
Seixas, Elsa
Velho, Tiago R.
Pedroso, Dora
Barros, André
Martins, Rui
Carvalho, Nuno
Payen, Didier
Weis, Sebastian
Yi, Hyon-Seung
Shong, Minho
Moita, Luís F.
author_sort Santos, Isa
collection PubMed
description Sepsis is a life-threatening organ dysfunction condition caused by a dysregulated host response to an infection. Here we report that the circulating levels of growth and differentiation factor-15 (GDF15) are strongly increased in septic shock patients and correlate with mortality. In mice, we find that peptidoglycan is a potent ligand that signals through the TLR2-Myd88 axis for the secretion of GDF15, and that Gdf15-deficient mice are protected against abdominal sepsis due to increased chemokine CXC ligand 5 (CXCL5)-mediated recruitment of neutrophils into the peritoneum, leading to better local bacterial control. Our results identify GDF15 as a potential target to improve sepsis treatment. Its inhibition should increase neutrophil recruitment to the site of infection and consequently lead to better pathogen control and clearance.
format Online
Article
Text
id pubmed-7275717
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-72757172020-06-11 CXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis Santos, Isa Colaço, Henrique G. Neves-Costa, Ana Seixas, Elsa Velho, Tiago R. Pedroso, Dora Barros, André Martins, Rui Carvalho, Nuno Payen, Didier Weis, Sebastian Yi, Hyon-Seung Shong, Minho Moita, Luís F. Proc Natl Acad Sci U S A Biological Sciences Sepsis is a life-threatening organ dysfunction condition caused by a dysregulated host response to an infection. Here we report that the circulating levels of growth and differentiation factor-15 (GDF15) are strongly increased in septic shock patients and correlate with mortality. In mice, we find that peptidoglycan is a potent ligand that signals through the TLR2-Myd88 axis for the secretion of GDF15, and that Gdf15-deficient mice are protected against abdominal sepsis due to increased chemokine CXC ligand 5 (CXCL5)-mediated recruitment of neutrophils into the peritoneum, leading to better local bacterial control. Our results identify GDF15 as a potential target to improve sepsis treatment. Its inhibition should increase neutrophil recruitment to the site of infection and consequently lead to better pathogen control and clearance. National Academy of Sciences 2020-06-02 2020-05-18 /pmc/articles/PMC7275717/ /pubmed/32424099 http://dx.doi.org/10.1073/pnas.1918508117 Text en Copyright © 2020 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Santos, Isa
Colaço, Henrique G.
Neves-Costa, Ana
Seixas, Elsa
Velho, Tiago R.
Pedroso, Dora
Barros, André
Martins, Rui
Carvalho, Nuno
Payen, Didier
Weis, Sebastian
Yi, Hyon-Seung
Shong, Minho
Moita, Luís F.
CXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis
title CXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis
title_full CXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis
title_fullStr CXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis
title_full_unstemmed CXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis
title_short CXCL5-mediated recruitment of neutrophils into the peritoneal cavity of Gdf15-deficient mice protects against abdominal sepsis
title_sort cxcl5-mediated recruitment of neutrophils into the peritoneal cavity of gdf15-deficient mice protects against abdominal sepsis
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275717/
https://www.ncbi.nlm.nih.gov/pubmed/32424099
http://dx.doi.org/10.1073/pnas.1918508117
work_keys_str_mv AT santosisa cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT colacohenriqueg cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT nevescostaana cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT seixaselsa cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT velhotiagor cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT pedrosodora cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT barrosandre cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT martinsrui cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT carvalhonuno cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT payendidier cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT weissebastian cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT yihyonseung cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT shongminho cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis
AT moitaluisf cxcl5mediatedrecruitmentofneutrophilsintotheperitonealcavityofgdf15deficientmiceprotectsagainstabdominalsepsis