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Autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways

The basic understanding of inflammatory airway diseases greatly benefits from imaging the cellular dynamics of immune cells. Current imaging approaches focus on labeling specific cells to follow their dynamics but fail to visualize the surrounding tissue. To overcome this problem, we evaluated autof...

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Autores principales: Kretschmer, Sarah, Pieper, Mario, Hüttmann, Gereon, Bölke, Torsten, Wollenberg, Barbara, Marsh, Leigh M, Garn, Holger, König, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972900/
https://www.ncbi.nlm.nih.gov/pubmed/27400364
http://dx.doi.org/10.1038/labinvest.2016.69
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author Kretschmer, Sarah
Pieper, Mario
Hüttmann, Gereon
Bölke, Torsten
Wollenberg, Barbara
Marsh, Leigh M
Garn, Holger
König, Peter
author_facet Kretschmer, Sarah
Pieper, Mario
Hüttmann, Gereon
Bölke, Torsten
Wollenberg, Barbara
Marsh, Leigh M
Garn, Holger
König, Peter
author_sort Kretschmer, Sarah
collection PubMed
description The basic understanding of inflammatory airway diseases greatly benefits from imaging the cellular dynamics of immune cells. Current imaging approaches focus on labeling specific cells to follow their dynamics but fail to visualize the surrounding tissue. To overcome this problem, we evaluated autofluorescence multiphoton microscopy for following the motion and interaction of cells in the airways in the context of tissue morphology. Freshly isolated murine tracheae from healthy mice and mice with experimental allergic airway inflammation were examined by autofluorescence multiphoton microscopy. In addition, fluorescently labeled ovalbumin and fluorophore-labeled antibodies were applied to visualize antigen uptake and to identify specific cell populations, respectively. The trachea in living mice was imaged to verify that the ex vivo preparation reflects the in vivo situation. Autofluorescence multiphoton microscopy was also tested to examine human tissue from patients in short-term tissue culture. Using autofluorescence, the epithelium, underlying cells, and fibers of the connective tissue, as well as blood vessels, were identified in isolated tracheae. Similar structures were visualized in living mice and in the human airway tissue. In explanted murine airways, mobile cells were localized within the tissue and we could follow their migration, interactions between individual cells, and their phagocytic activity. During allergic airway inflammation, increased number of eosinophil and neutrophil granulocytes were detected that moved within the connective tissue and immediately below the epithelium without damaging the epithelial cells or connective tissues. Contacts between granulocytes were transient lasting 3 min on average. Unexpectedly, prolonged interactions between granulocytes and antigen-uptaking cells were observed lasting for an average of 13 min. Our results indicate that autofluorescence-based imaging can detect previously unknown immune cell interactions in the airways. The method also holds the potential to be used during diagnostic procedures in humans if integrated into a bronchoscope.
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spelling pubmed-49729002016-08-17 Autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways Kretschmer, Sarah Pieper, Mario Hüttmann, Gereon Bölke, Torsten Wollenberg, Barbara Marsh, Leigh M Garn, Holger König, Peter Lab Invest Technical Report The basic understanding of inflammatory airway diseases greatly benefits from imaging the cellular dynamics of immune cells. Current imaging approaches focus on labeling specific cells to follow their dynamics but fail to visualize the surrounding tissue. To overcome this problem, we evaluated autofluorescence multiphoton microscopy for following the motion and interaction of cells in the airways in the context of tissue morphology. Freshly isolated murine tracheae from healthy mice and mice with experimental allergic airway inflammation were examined by autofluorescence multiphoton microscopy. In addition, fluorescently labeled ovalbumin and fluorophore-labeled antibodies were applied to visualize antigen uptake and to identify specific cell populations, respectively. The trachea in living mice was imaged to verify that the ex vivo preparation reflects the in vivo situation. Autofluorescence multiphoton microscopy was also tested to examine human tissue from patients in short-term tissue culture. Using autofluorescence, the epithelium, underlying cells, and fibers of the connective tissue, as well as blood vessels, were identified in isolated tracheae. Similar structures were visualized in living mice and in the human airway tissue. In explanted murine airways, mobile cells were localized within the tissue and we could follow their migration, interactions between individual cells, and their phagocytic activity. During allergic airway inflammation, increased number of eosinophil and neutrophil granulocytes were detected that moved within the connective tissue and immediately below the epithelium without damaging the epithelial cells or connective tissues. Contacts between granulocytes were transient lasting 3 min on average. Unexpectedly, prolonged interactions between granulocytes and antigen-uptaking cells were observed lasting for an average of 13 min. Our results indicate that autofluorescence-based imaging can detect previously unknown immune cell interactions in the airways. The method also holds the potential to be used during diagnostic procedures in humans if integrated into a bronchoscope. Nature Publishing Group 2016-08 2016-07-11 /pmc/articles/PMC4972900/ /pubmed/27400364 http://dx.doi.org/10.1038/labinvest.2016.69 Text en Copyright © 2016 United States & Canadian Academy of Pathology http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Technical Report
Kretschmer, Sarah
Pieper, Mario
Hüttmann, Gereon
Bölke, Torsten
Wollenberg, Barbara
Marsh, Leigh M
Garn, Holger
König, Peter
Autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways
title Autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways
title_full Autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways
title_fullStr Autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways
title_full_unstemmed Autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways
title_short Autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways
title_sort autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways
topic Technical Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972900/
https://www.ncbi.nlm.nih.gov/pubmed/27400364
http://dx.doi.org/10.1038/labinvest.2016.69
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