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Flagellin shifts 3D bronchospheres towards mucus hyperproduction

Cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD) are associated with acute and chronic bacterial infections of the lung. Excessive differentiation of basal cells to mucus-producing goblet cells can result in mucus hyperproduction and loss of mucociliary clearance in the airways...

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Autores principales: Sprott, Richard F., Ritzmann, Felix, Langer, Frank, Yao, Yiwen, Herr, Christian, Kohl, Yvonne, Tschernig, Thomas, Bals, Robert, Beisswenger, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448433/
https://www.ncbi.nlm.nih.gov/pubmed/32847538
http://dx.doi.org/10.1186/s12931-020-01486-x
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author Sprott, Richard F.
Ritzmann, Felix
Langer, Frank
Yao, Yiwen
Herr, Christian
Kohl, Yvonne
Tschernig, Thomas
Bals, Robert
Beisswenger, Christoph
author_facet Sprott, Richard F.
Ritzmann, Felix
Langer, Frank
Yao, Yiwen
Herr, Christian
Kohl, Yvonne
Tschernig, Thomas
Bals, Robert
Beisswenger, Christoph
author_sort Sprott, Richard F.
collection PubMed
description Cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD) are associated with acute and chronic bacterial infections of the lung. Excessive differentiation of basal cells to mucus-producing goblet cells can result in mucus hyperproduction and loss of mucociliary clearance in the airways of CF and COPD patients. Here, we aimed to investigate the effect of pathogen-associated molecular patterns (PAMPs) on the differentiation of human 3D bronchospheres. Primary human bronchial epithelial cells (HBECs) were differentiated to bronchospheres in the presence of bacterial flagellin and LPS and the synthetic Toll-like receptor (TLR) ligands Pam3CSK4 (TLR-2) and polyinosinic:polycytidylic acid (pIC, TLR-3). Electron and fluorescence microscopy showed that the differentiation of bronchospheres associated with the formation of lumina and appearance of cilia within 30 days after seeding. Incubation with flagellin resulted in a decreased formation of lumina and loss of cilia formation. Incubation with Pam3CSK, pIC, and LPS did not significantly affect formation of lumina and ciliation. Mucus production was strongly increased in response to flagellin and, to a lesser degree, in response to Pam3CSK4. Our results indicate that bacterial factors, such as flagellin, drive the differentiation of the respiratory epithelium towards mucus hyperproduction.
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spelling pubmed-74484332020-08-27 Flagellin shifts 3D bronchospheres towards mucus hyperproduction Sprott, Richard F. Ritzmann, Felix Langer, Frank Yao, Yiwen Herr, Christian Kohl, Yvonne Tschernig, Thomas Bals, Robert Beisswenger, Christoph Respir Res Letter to the Editor Cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD) are associated with acute and chronic bacterial infections of the lung. Excessive differentiation of basal cells to mucus-producing goblet cells can result in mucus hyperproduction and loss of mucociliary clearance in the airways of CF and COPD patients. Here, we aimed to investigate the effect of pathogen-associated molecular patterns (PAMPs) on the differentiation of human 3D bronchospheres. Primary human bronchial epithelial cells (HBECs) were differentiated to bronchospheres in the presence of bacterial flagellin and LPS and the synthetic Toll-like receptor (TLR) ligands Pam3CSK4 (TLR-2) and polyinosinic:polycytidylic acid (pIC, TLR-3). Electron and fluorescence microscopy showed that the differentiation of bronchospheres associated with the formation of lumina and appearance of cilia within 30 days after seeding. Incubation with flagellin resulted in a decreased formation of lumina and loss of cilia formation. Incubation with Pam3CSK, pIC, and LPS did not significantly affect formation of lumina and ciliation. Mucus production was strongly increased in response to flagellin and, to a lesser degree, in response to Pam3CSK4. Our results indicate that bacterial factors, such as flagellin, drive the differentiation of the respiratory epithelium towards mucus hyperproduction. BioMed Central 2020-08-26 2020 /pmc/articles/PMC7448433/ /pubmed/32847538 http://dx.doi.org/10.1186/s12931-020-01486-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Letter to the Editor
Sprott, Richard F.
Ritzmann, Felix
Langer, Frank
Yao, Yiwen
Herr, Christian
Kohl, Yvonne
Tschernig, Thomas
Bals, Robert
Beisswenger, Christoph
Flagellin shifts 3D bronchospheres towards mucus hyperproduction
title Flagellin shifts 3D bronchospheres towards mucus hyperproduction
title_full Flagellin shifts 3D bronchospheres towards mucus hyperproduction
title_fullStr Flagellin shifts 3D bronchospheres towards mucus hyperproduction
title_full_unstemmed Flagellin shifts 3D bronchospheres towards mucus hyperproduction
title_short Flagellin shifts 3D bronchospheres towards mucus hyperproduction
title_sort flagellin shifts 3d bronchospheres towards mucus hyperproduction
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448433/
https://www.ncbi.nlm.nih.gov/pubmed/32847538
http://dx.doi.org/10.1186/s12931-020-01486-x
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