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Stromal Cells Covering Omental Fat-Associated Lymphoid Clusters Trigger Formation of Neutrophil Aggregates to Capture Peritoneal Contaminants

The omentum is a visceral adipose tissue rich in fat-associated lymphoid clusters (FALCs) that collects peritoneal contaminants and provides a first layer of immunological defense within the abdomen. Here, we investigated the mechanisms that mediate the capture of peritoneal contaminants during peri...

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Autores principales: Jackson-Jones, Lucy Helen, Smith, Peter, Portman, Jordan Raymond, Magalhaes, Marlène Sophie, Mylonas, Katie Jude, Vermeren, Matthieu Marie, Nixon, Mark, Henderson, Beth Emily Pollot, Dobie, Ross, Vermeren, Sonja, Denby, Laura, Henderson, Neil Cowan, Mole, Damian James, Bénézech, Cécile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7156918/
https://www.ncbi.nlm.nih.gov/pubmed/32294409
http://dx.doi.org/10.1016/j.immuni.2020.03.011
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author Jackson-Jones, Lucy Helen
Smith, Peter
Portman, Jordan Raymond
Magalhaes, Marlène Sophie
Mylonas, Katie Jude
Vermeren, Matthieu Marie
Nixon, Mark
Henderson, Beth Emily Pollot
Dobie, Ross
Vermeren, Sonja
Denby, Laura
Henderson, Neil Cowan
Mole, Damian James
Bénézech, Cécile
author_facet Jackson-Jones, Lucy Helen
Smith, Peter
Portman, Jordan Raymond
Magalhaes, Marlène Sophie
Mylonas, Katie Jude
Vermeren, Matthieu Marie
Nixon, Mark
Henderson, Beth Emily Pollot
Dobie, Ross
Vermeren, Sonja
Denby, Laura
Henderson, Neil Cowan
Mole, Damian James
Bénézech, Cécile
author_sort Jackson-Jones, Lucy Helen
collection PubMed
description The omentum is a visceral adipose tissue rich in fat-associated lymphoid clusters (FALCs) that collects peritoneal contaminants and provides a first layer of immunological defense within the abdomen. Here, we investigated the mechanisms that mediate the capture of peritoneal contaminants during peritonitis. Single-cell RNA sequencing and spatial analysis of omental stromal cells revealed that the surface of FALCs were covered by CXCL1(+) mesothelial cells, which we termed FALC cover cells. Blockade of CXCL1 inhibited the recruitment and aggregation of neutrophils at FALCs during zymosan-induced peritonitis. Inhibition of protein arginine deiminase 4, an enzyme important for the release of neutrophil extracellular traps, abolished neutrophil aggregation and the capture of peritoneal contaminants by omental FALCs. Analysis of omental samples from patients with acute appendicitis confirmed neutrophil recruitment and bacterial capture at FALCs. Thus, specialized omental mesothelial cells coordinate the recruitment and aggregation of neutrophils to capture peritoneal contaminants.
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spelling pubmed-71569182020-04-22 Stromal Cells Covering Omental Fat-Associated Lymphoid Clusters Trigger Formation of Neutrophil Aggregates to Capture Peritoneal Contaminants Jackson-Jones, Lucy Helen Smith, Peter Portman, Jordan Raymond Magalhaes, Marlène Sophie Mylonas, Katie Jude Vermeren, Matthieu Marie Nixon, Mark Henderson, Beth Emily Pollot Dobie, Ross Vermeren, Sonja Denby, Laura Henderson, Neil Cowan Mole, Damian James Bénézech, Cécile Immunity Article The omentum is a visceral adipose tissue rich in fat-associated lymphoid clusters (FALCs) that collects peritoneal contaminants and provides a first layer of immunological defense within the abdomen. Here, we investigated the mechanisms that mediate the capture of peritoneal contaminants during peritonitis. Single-cell RNA sequencing and spatial analysis of omental stromal cells revealed that the surface of FALCs were covered by CXCL1(+) mesothelial cells, which we termed FALC cover cells. Blockade of CXCL1 inhibited the recruitment and aggregation of neutrophils at FALCs during zymosan-induced peritonitis. Inhibition of protein arginine deiminase 4, an enzyme important for the release of neutrophil extracellular traps, abolished neutrophil aggregation and the capture of peritoneal contaminants by omental FALCs. Analysis of omental samples from patients with acute appendicitis confirmed neutrophil recruitment and bacterial capture at FALCs. Thus, specialized omental mesothelial cells coordinate the recruitment and aggregation of neutrophils to capture peritoneal contaminants. Cell Press 2020-04-14 /pmc/articles/PMC7156918/ /pubmed/32294409 http://dx.doi.org/10.1016/j.immuni.2020.03.011 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jackson-Jones, Lucy Helen
Smith, Peter
Portman, Jordan Raymond
Magalhaes, Marlène Sophie
Mylonas, Katie Jude
Vermeren, Matthieu Marie
Nixon, Mark
Henderson, Beth Emily Pollot
Dobie, Ross
Vermeren, Sonja
Denby, Laura
Henderson, Neil Cowan
Mole, Damian James
Bénézech, Cécile
Stromal Cells Covering Omental Fat-Associated Lymphoid Clusters Trigger Formation of Neutrophil Aggregates to Capture Peritoneal Contaminants
title Stromal Cells Covering Omental Fat-Associated Lymphoid Clusters Trigger Formation of Neutrophil Aggregates to Capture Peritoneal Contaminants
title_full Stromal Cells Covering Omental Fat-Associated Lymphoid Clusters Trigger Formation of Neutrophil Aggregates to Capture Peritoneal Contaminants
title_fullStr Stromal Cells Covering Omental Fat-Associated Lymphoid Clusters Trigger Formation of Neutrophil Aggregates to Capture Peritoneal Contaminants
title_full_unstemmed Stromal Cells Covering Omental Fat-Associated Lymphoid Clusters Trigger Formation of Neutrophil Aggregates to Capture Peritoneal Contaminants
title_short Stromal Cells Covering Omental Fat-Associated Lymphoid Clusters Trigger Formation of Neutrophil Aggregates to Capture Peritoneal Contaminants
title_sort stromal cells covering omental fat-associated lymphoid clusters trigger formation of neutrophil aggregates to capture peritoneal contaminants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7156918/
https://www.ncbi.nlm.nih.gov/pubmed/32294409
http://dx.doi.org/10.1016/j.immuni.2020.03.011
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