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The influence of topographic microstructures on the initial adhesion of L929 fibroblasts studied by single-cell force spectroscopy
Single-cell force spectroscopy was used to investigate the initial adhesion of L929 fibroblasts onto periodically grooved titanium microstructures (height ~6 μm, groove width 20 μm). The position-dependent local adhesion strength of the cells was correlated with their rheological behavior. Spherical...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045512/ https://www.ncbi.nlm.nih.gov/pubmed/21153809 http://dx.doi.org/10.1007/s00249-010-0649-0 |
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author | Elter, Patrick Weihe, Thomas Lange, Regina Gimsa, Jan Beck, Ulrich |
author_facet | Elter, Patrick Weihe, Thomas Lange, Regina Gimsa, Jan Beck, Ulrich |
author_sort | Elter, Patrick |
collection | PubMed |
description | Single-cell force spectroscopy was used to investigate the initial adhesion of L929 fibroblasts onto periodically grooved titanium microstructures (height ~6 μm, groove width 20 μm). The position-dependent local adhesion strength of the cells was correlated with their rheological behavior. Spherical cells exhibited a significantly lower Young’s modulus (<1 kPa) than that reported for spread cells, and their elastic properties can roughly be explained by the Hertz model for an elastic sphere. While in contact with the planar regions of the substrate, the cells started to adapt their shape through slight ventral flattening. The process was found to be independent of the applied contact force for values between 100 and 1,000 pN. The degree of flattening correlated with the adhesion strength during the first 60 s. Adhesion strength can be described by fast exponential kinetics as [Formula: see text] with C (1) = 2.34 ± 0.19 nN and C (2) = 0.09 ± 0.02 s(−1). A significant drop in the adhesion strength of up to 50% was found near the groove edges. The effect can be interpreted by the geometric decrease of the contact area, which indicates the inability of the fibroblasts to adapt to the shape of the substrate. Our results explain the role of the substrate’s topography in contact guidance and suggest that rheological cell properties must be considered in cell adhesion modeling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00249-010-0649-0) contains supplementary material, which is available to authorized users. |
format | Text |
id | pubmed-3045512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-30455122011-04-04 The influence of topographic microstructures on the initial adhesion of L929 fibroblasts studied by single-cell force spectroscopy Elter, Patrick Weihe, Thomas Lange, Regina Gimsa, Jan Beck, Ulrich Eur Biophys J Original Paper Single-cell force spectroscopy was used to investigate the initial adhesion of L929 fibroblasts onto periodically grooved titanium microstructures (height ~6 μm, groove width 20 μm). The position-dependent local adhesion strength of the cells was correlated with their rheological behavior. Spherical cells exhibited a significantly lower Young’s modulus (<1 kPa) than that reported for spread cells, and their elastic properties can roughly be explained by the Hertz model for an elastic sphere. While in contact with the planar regions of the substrate, the cells started to adapt their shape through slight ventral flattening. The process was found to be independent of the applied contact force for values between 100 and 1,000 pN. The degree of flattening correlated with the adhesion strength during the first 60 s. Adhesion strength can be described by fast exponential kinetics as [Formula: see text] with C (1) = 2.34 ± 0.19 nN and C (2) = 0.09 ± 0.02 s(−1). A significant drop in the adhesion strength of up to 50% was found near the groove edges. The effect can be interpreted by the geometric decrease of the contact area, which indicates the inability of the fibroblasts to adapt to the shape of the substrate. Our results explain the role of the substrate’s topography in contact guidance and suggest that rheological cell properties must be considered in cell adhesion modeling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00249-010-0649-0) contains supplementary material, which is available to authorized users. Springer-Verlag 2010-12-14 2011 /pmc/articles/PMC3045512/ /pubmed/21153809 http://dx.doi.org/10.1007/s00249-010-0649-0 Text en © The Author(s) 2010 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 Elter, Patrick Weihe, Thomas Lange, Regina Gimsa, Jan Beck, Ulrich The influence of topographic microstructures on the initial adhesion of L929 fibroblasts studied by single-cell force spectroscopy |
title | The influence of topographic microstructures on the initial adhesion of L929 fibroblasts studied by single-cell force spectroscopy |
title_full | The influence of topographic microstructures on the initial adhesion of L929 fibroblasts studied by single-cell force spectroscopy |
title_fullStr | The influence of topographic microstructures on the initial adhesion of L929 fibroblasts studied by single-cell force spectroscopy |
title_full_unstemmed | The influence of topographic microstructures on the initial adhesion of L929 fibroblasts studied by single-cell force spectroscopy |
title_short | The influence of topographic microstructures on the initial adhesion of L929 fibroblasts studied by single-cell force spectroscopy |
title_sort | influence of topographic microstructures on the initial adhesion of l929 fibroblasts studied by single-cell force spectroscopy |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045512/ https://www.ncbi.nlm.nih.gov/pubmed/21153809 http://dx.doi.org/10.1007/s00249-010-0649-0 |
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