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Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation
BACKGROUND: Mesenchymal stem cells (MSC) are multipotent cells which can differentiate along osteogenic, chondrogenic, and adipogenic lineages. The present study was designed to investigate the influence of mechanical force as a specific physiological stress on the differentiation of (MSC) to osteob...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1483821/ https://www.ncbi.nlm.nih.gov/pubmed/16573842 http://dx.doi.org/10.1186/1746-160X-2-8 |
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author | Wiesmann, Anne Bühring, Hans-Jörg Mentrup, Christoph Wiesmann, Hans-Peter |
author_facet | Wiesmann, Anne Bühring, Hans-Jörg Mentrup, Christoph Wiesmann, Hans-Peter |
author_sort | Wiesmann, Anne |
collection | PubMed |
description | BACKGROUND: Mesenchymal stem cells (MSC) are multipotent cells which can differentiate along osteogenic, chondrogenic, and adipogenic lineages. The present study was designed to investigate the influence of mechanical force as a specific physiological stress on the differentiation of (MSC) to osteoblast-like cells. METHODS: Human MSC were cultured in osteoinductive medium with or without cyclic uniaxial mechanical stimulation (2000 μstrain, 200 cycles per day, 1 Hz). Cultured cells were analysed for expression of collagen type I, osteocalcin, osteonectin, and CD90. To evaluate the biomineral formation the content of bound calcium in the cultures was determined. RESULTS: After 14 days in culture immunfluorescence staining revealed enhancement of collagen type I and osteonectin expression in response to mechanical stimulation. In contrast, mechanically stimulated cultures stained negative for CD90. In stimulated and unstimulated cultures an increase in the calcium content over time was observed. After 21 days in culture the calcium content in mechanical stimulated cultures was significantly higher compared to unstimulated control cultures. CONCLUSION: These results demonstrate the influence of mechanical force on the differentiation of human MSC into osteoblast-like cells in vitro. While significant enhancement of the biomineral formation by mechanical stimulation is not detected before 21 days, effects on the extracellular matrix became already obvious after 14 days. The decrease of CD90 expression in mechanically stimulated cultures compared to unstimulated control cultures suggests that CD90 is only transiently expressed expression during the differentiation of MSC to osteoblast-like cells in culture. |
format | Text |
id | pubmed-1483821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-14838212006-06-29 Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation Wiesmann, Anne Bühring, Hans-Jörg Mentrup, Christoph Wiesmann, Hans-Peter Head Face Med Research BACKGROUND: Mesenchymal stem cells (MSC) are multipotent cells which can differentiate along osteogenic, chondrogenic, and adipogenic lineages. The present study was designed to investigate the influence of mechanical force as a specific physiological stress on the differentiation of (MSC) to osteoblast-like cells. METHODS: Human MSC were cultured in osteoinductive medium with or without cyclic uniaxial mechanical stimulation (2000 μstrain, 200 cycles per day, 1 Hz). Cultured cells were analysed for expression of collagen type I, osteocalcin, osteonectin, and CD90. To evaluate the biomineral formation the content of bound calcium in the cultures was determined. RESULTS: After 14 days in culture immunfluorescence staining revealed enhancement of collagen type I and osteonectin expression in response to mechanical stimulation. In contrast, mechanically stimulated cultures stained negative for CD90. In stimulated and unstimulated cultures an increase in the calcium content over time was observed. After 21 days in culture the calcium content in mechanical stimulated cultures was significantly higher compared to unstimulated control cultures. CONCLUSION: These results demonstrate the influence of mechanical force on the differentiation of human MSC into osteoblast-like cells in vitro. While significant enhancement of the biomineral formation by mechanical stimulation is not detected before 21 days, effects on the extracellular matrix became already obvious after 14 days. The decrease of CD90 expression in mechanically stimulated cultures compared to unstimulated control cultures suggests that CD90 is only transiently expressed expression during the differentiation of MSC to osteoblast-like cells in culture. BioMed Central 2006-03-31 /pmc/articles/PMC1483821/ /pubmed/16573842 http://dx.doi.org/10.1186/1746-160X-2-8 Text en Copyright © 2006 Wiesmann et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Wiesmann, Anne Bühring, Hans-Jörg Mentrup, Christoph Wiesmann, Hans-Peter Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation |
title | Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation |
title_full | Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation |
title_fullStr | Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation |
title_full_unstemmed | Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation |
title_short | Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation |
title_sort | decreased cd90 expression in human mesenchymal stem cells by applying mechanical stimulation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1483821/ https://www.ncbi.nlm.nih.gov/pubmed/16573842 http://dx.doi.org/10.1186/1746-160X-2-8 |
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