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Complex morphology and functional dynamics of vital murine intestinal mucosa revealed by autofluorescence 2-photon microscopy
The mucosa of the gastrointestinal tract is a dynamic tissue composed of numerous cell types with complex cellular functions. Study of the vital intestinal mucosa has been hampered by lack of suitable model systems. We here present a novel animal model that enables highly resolved three-dimensional...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278620/ https://www.ncbi.nlm.nih.gov/pubmed/22227801 http://dx.doi.org/10.1007/s00418-011-0905-0 |
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author | Klinger, Antje Orzekowsky-Schroeder, Regina von Smolinski, Dorthe Blessenohl, Maike Schueth, Anna Koop, Norbert Huettmann, Gereon Gebert, Andreas |
author_facet | Klinger, Antje Orzekowsky-Schroeder, Regina von Smolinski, Dorthe Blessenohl, Maike Schueth, Anna Koop, Norbert Huettmann, Gereon Gebert, Andreas |
author_sort | Klinger, Antje |
collection | PubMed |
description | The mucosa of the gastrointestinal tract is a dynamic tissue composed of numerous cell types with complex cellular functions. Study of the vital intestinal mucosa has been hampered by lack of suitable model systems. We here present a novel animal model that enables highly resolved three-dimensional imaging of the vital murine intestine in anaesthetized mice. Using intravital autofluorescence 2-photon (A2P) microscopy we studied the choreographed interactions of enterocytes, goblet cells, enteroendocrine cells and brush cells with other cellular constituents of the small intestinal mucosa over several hours at a subcellular resolution and in three dimensions. Vigorously moving lymphoid cells and their interaction with constituent parts of the lamina propria were examined and quantitatively analyzed. Nuclear and lectin staining permitted simultaneous characterization of autofluorescence and admitted dyes and yielded additional spectral information that is crucial to the interpretation of the complex intestinal mucosa. This novel intravital approach provides detailed insights into the physiology of the small intestine and especially opens a new window for investigating cellular dynamics under nearly physiological conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00418-011-0905-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3278620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-32786202012-02-21 Complex morphology and functional dynamics of vital murine intestinal mucosa revealed by autofluorescence 2-photon microscopy Klinger, Antje Orzekowsky-Schroeder, Regina von Smolinski, Dorthe Blessenohl, Maike Schueth, Anna Koop, Norbert Huettmann, Gereon Gebert, Andreas Histochem Cell Biol Original Paper The mucosa of the gastrointestinal tract is a dynamic tissue composed of numerous cell types with complex cellular functions. Study of the vital intestinal mucosa has been hampered by lack of suitable model systems. We here present a novel animal model that enables highly resolved three-dimensional imaging of the vital murine intestine in anaesthetized mice. Using intravital autofluorescence 2-photon (A2P) microscopy we studied the choreographed interactions of enterocytes, goblet cells, enteroendocrine cells and brush cells with other cellular constituents of the small intestinal mucosa over several hours at a subcellular resolution and in three dimensions. Vigorously moving lymphoid cells and their interaction with constituent parts of the lamina propria were examined and quantitatively analyzed. Nuclear and lectin staining permitted simultaneous characterization of autofluorescence and admitted dyes and yielded additional spectral information that is crucial to the interpretation of the complex intestinal mucosa. This novel intravital approach provides detailed insights into the physiology of the small intestine and especially opens a new window for investigating cellular dynamics under nearly physiological conditions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00418-011-0905-0) contains supplementary material, which is available to authorized users. Springer-Verlag 2012-01-07 2012 /pmc/articles/PMC3278620/ /pubmed/22227801 http://dx.doi.org/10.1007/s00418-011-0905-0 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Paper Klinger, Antje Orzekowsky-Schroeder, Regina von Smolinski, Dorthe Blessenohl, Maike Schueth, Anna Koop, Norbert Huettmann, Gereon Gebert, Andreas Complex morphology and functional dynamics of vital murine intestinal mucosa revealed by autofluorescence 2-photon microscopy |
title | Complex morphology and functional dynamics of vital murine intestinal mucosa revealed by autofluorescence 2-photon microscopy |
title_full | Complex morphology and functional dynamics of vital murine intestinal mucosa revealed by autofluorescence 2-photon microscopy |
title_fullStr | Complex morphology and functional dynamics of vital murine intestinal mucosa revealed by autofluorescence 2-photon microscopy |
title_full_unstemmed | Complex morphology and functional dynamics of vital murine intestinal mucosa revealed by autofluorescence 2-photon microscopy |
title_short | Complex morphology and functional dynamics of vital murine intestinal mucosa revealed by autofluorescence 2-photon microscopy |
title_sort | complex morphology and functional dynamics of vital murine intestinal mucosa revealed by autofluorescence 2-photon microscopy |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278620/ https://www.ncbi.nlm.nih.gov/pubmed/22227801 http://dx.doi.org/10.1007/s00418-011-0905-0 |
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