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Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells

The small intestine is a complex system that carries out various functions. The main function of enterocytes is absorption of nutrients, whereas membranous cells (M cells) are responsible for delivering antigens/foreign substances to the mucosal lymphoid tissues. However, to get a fundamental unders...

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Autores principales: Schimpel, Christa, Werzer, Oliver, Fröhlich, Eleonore, Leitinger, Gerd, Absenger-Novak, Markus, Teubl, Birgit, Zimmer, Andreas, Roblegg, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505173/
https://www.ncbi.nlm.nih.gov/pubmed/26199850
http://dx.doi.org/10.3762/bjnano.6.151
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author Schimpel, Christa
Werzer, Oliver
Fröhlich, Eleonore
Leitinger, Gerd
Absenger-Novak, Markus
Teubl, Birgit
Zimmer, Andreas
Roblegg, Eva
author_facet Schimpel, Christa
Werzer, Oliver
Fröhlich, Eleonore
Leitinger, Gerd
Absenger-Novak, Markus
Teubl, Birgit
Zimmer, Andreas
Roblegg, Eva
author_sort Schimpel, Christa
collection PubMed
description The small intestine is a complex system that carries out various functions. The main function of enterocytes is absorption of nutrients, whereas membranous cells (M cells) are responsible for delivering antigens/foreign substances to the mucosal lymphoid tissues. However, to get a fundamental understanding of how cellular structures contribute to physiological processes, precise knowledge about surface morphologies, cytoskeleton organizations and biomechanical properties is necessary. Atomic force microscopy (AFM) was used here as a powerful tool to study surface topographies of Caco-2 cells and M cells. Furthermore, cell elasticity (i.e., the mechanical response of a cell on a tip indentation), was elucidated by force curve measurements. Besides elasticity, adhesion was evaluated by recording the attraction and repulsion forces between the tip and the cell surface. Organization of F-actin networks were investigated via phalloidin labeling and visualization was performed with confocal laser scanning fluorescence microscopy (CLSM) and scanning electron microscopy (SEM). The results of these various experimental techniques revealed significant differences in the cytoskeleton/microvilli arrangements and F-actin organization. Caco-2 cells displayed densely packed F-actin bundles covering the entire cell surface, indicating the formation of a well-differentiated brush border. In contrast, in M cells actins were arranged as short and/or truncated thin villi, only available at the cell edge. The elasticity of M cells was 1.7-fold higher compared to Caco-2 cells and increased significantly from the cell periphery to the nuclear region. Since elasticity can be directly linked to cell adhesion, M cells showed higher adhesion forces than Caco-2 cells. The combination of distinct experimental techniques shows that morphological differences between Caco-2 cells and M cells correlate with mechanical cell properties and provide useful information to understand physiological processes/mechanisms in the small intestine.
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spelling pubmed-45051732015-07-21 Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells Schimpel, Christa Werzer, Oliver Fröhlich, Eleonore Leitinger, Gerd Absenger-Novak, Markus Teubl, Birgit Zimmer, Andreas Roblegg, Eva Beilstein J Nanotechnol Full Research Paper The small intestine is a complex system that carries out various functions. The main function of enterocytes is absorption of nutrients, whereas membranous cells (M cells) are responsible for delivering antigens/foreign substances to the mucosal lymphoid tissues. However, to get a fundamental understanding of how cellular structures contribute to physiological processes, precise knowledge about surface morphologies, cytoskeleton organizations and biomechanical properties is necessary. Atomic force microscopy (AFM) was used here as a powerful tool to study surface topographies of Caco-2 cells and M cells. Furthermore, cell elasticity (i.e., the mechanical response of a cell on a tip indentation), was elucidated by force curve measurements. Besides elasticity, adhesion was evaluated by recording the attraction and repulsion forces between the tip and the cell surface. Organization of F-actin networks were investigated via phalloidin labeling and visualization was performed with confocal laser scanning fluorescence microscopy (CLSM) and scanning electron microscopy (SEM). The results of these various experimental techniques revealed significant differences in the cytoskeleton/microvilli arrangements and F-actin organization. Caco-2 cells displayed densely packed F-actin bundles covering the entire cell surface, indicating the formation of a well-differentiated brush border. In contrast, in M cells actins were arranged as short and/or truncated thin villi, only available at the cell edge. The elasticity of M cells was 1.7-fold higher compared to Caco-2 cells and increased significantly from the cell periphery to the nuclear region. Since elasticity can be directly linked to cell adhesion, M cells showed higher adhesion forces than Caco-2 cells. The combination of distinct experimental techniques shows that morphological differences between Caco-2 cells and M cells correlate with mechanical cell properties and provide useful information to understand physiological processes/mechanisms in the small intestine. Beilstein-Institut 2015-07-06 /pmc/articles/PMC4505173/ /pubmed/26199850 http://dx.doi.org/10.3762/bjnano.6.151 Text en Copyright © 2015, Schimpel et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjnano/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Nanotechnology terms and conditions: (https://www.beilstein-journals.org/bjnano/terms)
spellingShingle Full Research Paper
Schimpel, Christa
Werzer, Oliver
Fröhlich, Eleonore
Leitinger, Gerd
Absenger-Novak, Markus
Teubl, Birgit
Zimmer, Andreas
Roblegg, Eva
Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells
title Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells
title_full Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells
title_fullStr Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells
title_full_unstemmed Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells
title_short Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells
title_sort atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505173/
https://www.ncbi.nlm.nih.gov/pubmed/26199850
http://dx.doi.org/10.3762/bjnano.6.151
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