Cargando…

Fibrotic Lung Disease Alters Neutrophil Trafficking and Promotes Neutrophil Elastase and Extracellular Trap Release

Idiopathic pulmonary fibrosis (IPF) is a progressive, irreversible disease characterized by collagen deposition within the interstitium of the lung. This impairs gas exchange and results in eventual respiratory failure. Clinical studies show a correlation between elevated neutrophil numbers and IPF...

Descripción completa

Detalles Bibliográficos
Autores principales: Warheit-Niemi, Helen I., Huizinga, Gabrielle P., Edwards, Summer J., Wang, Yizhou, Murray, Susan K., O’Dwyer, David N., Moore, Bethany B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542701/
https://www.ncbi.nlm.nih.gov/pubmed/36534439
http://dx.doi.org/10.4049/immunohorizons.2200083
_version_ 1785114148377460736
author Warheit-Niemi, Helen I.
Huizinga, Gabrielle P.
Edwards, Summer J.
Wang, Yizhou
Murray, Susan K.
O’Dwyer, David N.
Moore, Bethany B.
author_facet Warheit-Niemi, Helen I.
Huizinga, Gabrielle P.
Edwards, Summer J.
Wang, Yizhou
Murray, Susan K.
O’Dwyer, David N.
Moore, Bethany B.
author_sort Warheit-Niemi, Helen I.
collection PubMed
description Idiopathic pulmonary fibrosis (IPF) is a progressive, irreversible disease characterized by collagen deposition within the interstitium of the lung. This impairs gas exchange and results in eventual respiratory failure. Clinical studies show a correlation between elevated neutrophil numbers and IPF disease progression; however, the mechanistic roles neutrophils play in this disease are not well described. In the present study, we describe alterations to the trafficking and function of neutrophils after the development of fibrosis. We observed increased numbers of total and aged neutrophils in peripheral tissues of fibrotic mice. This appeared to be driven by an upregulation of neutrophil chemokine Cxcl2 by lung cells. In addition, neutrophil recruitment back to the bone marrow for clearance appeared to be impaired, because we saw decreased aged neutrophils in the bone marrow of fibrotic mice. Neutrophils in fibrosis were activated, because ex vivo assays showed increased elastase and extracellular trap release by neutrophils from fibrotic mice. This likely mediated disease exacerbation, because mice exhibiting a progressive disease phenotype with greater weight loss and mortality had more activated neutrophils and increased levels of extracellular DNA present in their lungs than did mice with a nonprogressive disease phenotype. These findings further our understanding of the dynamics of neutrophil populations and their trafficking in progressive fibrotic lung disease and may help inform treatments targeting neutrophil function for patients with IPF experiencing disease exacerbation in the future.
format Online
Article
Text
id pubmed-10542701
institution National Center for Biotechnology Information
language English
publishDate 2022
record_format MEDLINE/PubMed
spelling pubmed-105427012023-10-02 Fibrotic Lung Disease Alters Neutrophil Trafficking and Promotes Neutrophil Elastase and Extracellular Trap Release Warheit-Niemi, Helen I. Huizinga, Gabrielle P. Edwards, Summer J. Wang, Yizhou Murray, Susan K. O’Dwyer, David N. Moore, Bethany B. Immunohorizons Article Idiopathic pulmonary fibrosis (IPF) is a progressive, irreversible disease characterized by collagen deposition within the interstitium of the lung. This impairs gas exchange and results in eventual respiratory failure. Clinical studies show a correlation between elevated neutrophil numbers and IPF disease progression; however, the mechanistic roles neutrophils play in this disease are not well described. In the present study, we describe alterations to the trafficking and function of neutrophils after the development of fibrosis. We observed increased numbers of total and aged neutrophils in peripheral tissues of fibrotic mice. This appeared to be driven by an upregulation of neutrophil chemokine Cxcl2 by lung cells. In addition, neutrophil recruitment back to the bone marrow for clearance appeared to be impaired, because we saw decreased aged neutrophils in the bone marrow of fibrotic mice. Neutrophils in fibrosis were activated, because ex vivo assays showed increased elastase and extracellular trap release by neutrophils from fibrotic mice. This likely mediated disease exacerbation, because mice exhibiting a progressive disease phenotype with greater weight loss and mortality had more activated neutrophils and increased levels of extracellular DNA present in their lungs than did mice with a nonprogressive disease phenotype. These findings further our understanding of the dynamics of neutrophil populations and their trafficking in progressive fibrotic lung disease and may help inform treatments targeting neutrophil function for patients with IPF experiencing disease exacerbation in the future. 2022-12-01 /pmc/articles/PMC10542701/ /pubmed/36534439 http://dx.doi.org/10.4049/immunohorizons.2200083 Text en https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the CC BY 4.0 Unported license.
spellingShingle Article
Warheit-Niemi, Helen I.
Huizinga, Gabrielle P.
Edwards, Summer J.
Wang, Yizhou
Murray, Susan K.
O’Dwyer, David N.
Moore, Bethany B.
Fibrotic Lung Disease Alters Neutrophil Trafficking and Promotes Neutrophil Elastase and Extracellular Trap Release
title Fibrotic Lung Disease Alters Neutrophil Trafficking and Promotes Neutrophil Elastase and Extracellular Trap Release
title_full Fibrotic Lung Disease Alters Neutrophil Trafficking and Promotes Neutrophil Elastase and Extracellular Trap Release
title_fullStr Fibrotic Lung Disease Alters Neutrophil Trafficking and Promotes Neutrophil Elastase and Extracellular Trap Release
title_full_unstemmed Fibrotic Lung Disease Alters Neutrophil Trafficking and Promotes Neutrophil Elastase and Extracellular Trap Release
title_short Fibrotic Lung Disease Alters Neutrophil Trafficking and Promotes Neutrophil Elastase and Extracellular Trap Release
title_sort fibrotic lung disease alters neutrophil trafficking and promotes neutrophil elastase and extracellular trap release
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542701/
https://www.ncbi.nlm.nih.gov/pubmed/36534439
http://dx.doi.org/10.4049/immunohorizons.2200083
work_keys_str_mv AT warheitniemiheleni fibroticlungdiseasealtersneutrophiltraffickingandpromotesneutrophilelastaseandextracellulartraprelease
AT huizingagabriellep fibroticlungdiseasealtersneutrophiltraffickingandpromotesneutrophilelastaseandextracellulartraprelease
AT edwardssummerj fibroticlungdiseasealtersneutrophiltraffickingandpromotesneutrophilelastaseandextracellulartraprelease
AT wangyizhou fibroticlungdiseasealtersneutrophiltraffickingandpromotesneutrophilelastaseandextracellulartraprelease
AT murraysusank fibroticlungdiseasealtersneutrophiltraffickingandpromotesneutrophilelastaseandextracellulartraprelease
AT odwyerdavidn fibroticlungdiseasealtersneutrophiltraffickingandpromotesneutrophilelastaseandextracellulartraprelease
AT moorebethanyb fibroticlungdiseasealtersneutrophiltraffickingandpromotesneutrophilelastaseandextracellulartraprelease