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Cytokine–Ion Channel Interactions in Pulmonary Inflammation
The lungs conceptually represent a sponge that is interposed in series in the bodies’ systemic circulation to take up oxygen and eliminate carbon dioxide. As such, it matches the huge surface areas of the alveolar epithelium to the pulmonary blood capillaries. The lung’s constant exposure to the ext...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758508/ https://www.ncbi.nlm.nih.gov/pubmed/29354115 http://dx.doi.org/10.3389/fimmu.2017.01644 |
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author | Hamacher, Jürg Hadizamani, Yalda Borgmann, Michèle Mohaupt, Markus Männel, Daniela Narcissa Moehrlen, Ueli Lucas, Rudolf Stammberger, Uz |
author_facet | Hamacher, Jürg Hadizamani, Yalda Borgmann, Michèle Mohaupt, Markus Männel, Daniela Narcissa Moehrlen, Ueli Lucas, Rudolf Stammberger, Uz |
author_sort | Hamacher, Jürg |
collection | PubMed |
description | The lungs conceptually represent a sponge that is interposed in series in the bodies’ systemic circulation to take up oxygen and eliminate carbon dioxide. As such, it matches the huge surface areas of the alveolar epithelium to the pulmonary blood capillaries. The lung’s constant exposure to the exterior necessitates a competent immune system, as evidenced by the association of clinical immunodeficiencies with pulmonary infections. From the in utero to the postnatal and adult situation, there is an inherent vital need to manage alveolar fluid reabsorption, be it postnatally, or in case of hydrostatic or permeability edema. Whereas a wealth of literature exists on the physiological basis of fluid and solute reabsorption by ion channels and water pores, only sparse knowledge is available so far on pathological situations, such as in microbial infection, acute lung injury or acute respiratory distress syndrome, and in the pulmonary reimplantation response in transplanted lungs. The aim of this review is to discuss alveolar liquid clearance in a selection of lung injury models, thereby especially focusing on cytokines and mediators that modulate ion channels. Inflammation is characterized by complex and probably time-dependent co-signaling, interactions between the involved cell types, as well as by cell demise and barrier dysfunction, which may not uniquely determine a clinical picture. This review, therefore, aims to give integrative thoughts and wants to foster the unraveling of unmet needs in future research. |
format | Online Article Text |
id | pubmed-5758508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57585082018-01-19 Cytokine–Ion Channel Interactions in Pulmonary Inflammation Hamacher, Jürg Hadizamani, Yalda Borgmann, Michèle Mohaupt, Markus Männel, Daniela Narcissa Moehrlen, Ueli Lucas, Rudolf Stammberger, Uz Front Immunol Immunology The lungs conceptually represent a sponge that is interposed in series in the bodies’ systemic circulation to take up oxygen and eliminate carbon dioxide. As such, it matches the huge surface areas of the alveolar epithelium to the pulmonary blood capillaries. The lung’s constant exposure to the exterior necessitates a competent immune system, as evidenced by the association of clinical immunodeficiencies with pulmonary infections. From the in utero to the postnatal and adult situation, there is an inherent vital need to manage alveolar fluid reabsorption, be it postnatally, or in case of hydrostatic or permeability edema. Whereas a wealth of literature exists on the physiological basis of fluid and solute reabsorption by ion channels and water pores, only sparse knowledge is available so far on pathological situations, such as in microbial infection, acute lung injury or acute respiratory distress syndrome, and in the pulmonary reimplantation response in transplanted lungs. The aim of this review is to discuss alveolar liquid clearance in a selection of lung injury models, thereby especially focusing on cytokines and mediators that modulate ion channels. Inflammation is characterized by complex and probably time-dependent co-signaling, interactions between the involved cell types, as well as by cell demise and barrier dysfunction, which may not uniquely determine a clinical picture. This review, therefore, aims to give integrative thoughts and wants to foster the unraveling of unmet needs in future research. Frontiers Media S.A. 2018-01-04 /pmc/articles/PMC5758508/ /pubmed/29354115 http://dx.doi.org/10.3389/fimmu.2017.01644 Text en Copyright © 2018 Hamacher, Hadizamani, Borgmann, Mohaupt, Männel, Moehrlen, Lucas and Stammberger. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Hamacher, Jürg Hadizamani, Yalda Borgmann, Michèle Mohaupt, Markus Männel, Daniela Narcissa Moehrlen, Ueli Lucas, Rudolf Stammberger, Uz Cytokine–Ion Channel Interactions in Pulmonary Inflammation |
title | Cytokine–Ion Channel Interactions in Pulmonary Inflammation |
title_full | Cytokine–Ion Channel Interactions in Pulmonary Inflammation |
title_fullStr | Cytokine–Ion Channel Interactions in Pulmonary Inflammation |
title_full_unstemmed | Cytokine–Ion Channel Interactions in Pulmonary Inflammation |
title_short | Cytokine–Ion Channel Interactions in Pulmonary Inflammation |
title_sort | cytokine–ion channel interactions in pulmonary inflammation |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758508/ https://www.ncbi.nlm.nih.gov/pubmed/29354115 http://dx.doi.org/10.3389/fimmu.2017.01644 |
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