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Acute Lung Injury: How Macrophages Orchestrate Resolution of Inflammation and Tissue Repair

Lung macrophages are long living cells with broad differentiation potential, which reside in the lung interstitium and alveoli or are organ-recruited upon inflammatory stimuli. A role of resident and recruited macrophages in initiating and maintaining pulmonary inflammation in lung infection or inju...

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Autores principales: Herold, Susanne, Mayer, Konstantin, Lohmeyer, Juergen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342347/
https://www.ncbi.nlm.nih.gov/pubmed/22566854
http://dx.doi.org/10.3389/fimmu.2011.00065
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author Herold, Susanne
Mayer, Konstantin
Lohmeyer, Juergen
author_facet Herold, Susanne
Mayer, Konstantin
Lohmeyer, Juergen
author_sort Herold, Susanne
collection PubMed
description Lung macrophages are long living cells with broad differentiation potential, which reside in the lung interstitium and alveoli or are organ-recruited upon inflammatory stimuli. A role of resident and recruited macrophages in initiating and maintaining pulmonary inflammation in lung infection or injury has been convincingly demonstrated. More recent reports suggest that lung macrophages are main orchestrators of termination and resolution of inflammation. They are also initiators of parenchymal repair processes that are essential for return to homeostasis with normal gas exchange. In this review we will discuss cellular cross-talk mechanisms and molecular pathways of macrophage plasticity which define their role in inflammation resolution and in initiation of lung barrier repair following lung injury.
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spelling pubmed-33423472012-05-07 Acute Lung Injury: How Macrophages Orchestrate Resolution of Inflammation and Tissue Repair Herold, Susanne Mayer, Konstantin Lohmeyer, Juergen Front Immunol Immunology Lung macrophages are long living cells with broad differentiation potential, which reside in the lung interstitium and alveoli or are organ-recruited upon inflammatory stimuli. A role of resident and recruited macrophages in initiating and maintaining pulmonary inflammation in lung infection or injury has been convincingly demonstrated. More recent reports suggest that lung macrophages are main orchestrators of termination and resolution of inflammation. They are also initiators of parenchymal repair processes that are essential for return to homeostasis with normal gas exchange. In this review we will discuss cellular cross-talk mechanisms and molecular pathways of macrophage plasticity which define their role in inflammation resolution and in initiation of lung barrier repair following lung injury. Frontiers Research Foundation 2011-11-24 /pmc/articles/PMC3342347/ /pubmed/22566854 http://dx.doi.org/10.3389/fimmu.2011.00065 Text en Copyright © 2011 Herold, Mayer and Lohmeyer. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Immunology
Herold, Susanne
Mayer, Konstantin
Lohmeyer, Juergen
Acute Lung Injury: How Macrophages Orchestrate Resolution of Inflammation and Tissue Repair
title Acute Lung Injury: How Macrophages Orchestrate Resolution of Inflammation and Tissue Repair
title_full Acute Lung Injury: How Macrophages Orchestrate Resolution of Inflammation and Tissue Repair
title_fullStr Acute Lung Injury: How Macrophages Orchestrate Resolution of Inflammation and Tissue Repair
title_full_unstemmed Acute Lung Injury: How Macrophages Orchestrate Resolution of Inflammation and Tissue Repair
title_short Acute Lung Injury: How Macrophages Orchestrate Resolution of Inflammation and Tissue Repair
title_sort acute lung injury: how macrophages orchestrate resolution of inflammation and tissue repair
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342347/
https://www.ncbi.nlm.nih.gov/pubmed/22566854
http://dx.doi.org/10.3389/fimmu.2011.00065
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