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Ultrastructural changes during osteogenic differentiation in mesenchymal stromal cells cultured in alginate hydrogel
BACKGROUND: Osteogenic differentiation of mesenchymal stem cells has been extensively investigated with regards to different aspects, including the analysis of cell intracellular and extracellular proteome, cell gene expression pattern, and morphology. During the osteogenic differentiation, osteobla...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210287/ https://www.ncbi.nlm.nih.gov/pubmed/28066541 http://dx.doi.org/10.1186/s13578-016-0128-0 |
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author | Grzesiak, Jakub Śmieszek, Agnieszka Marycz, Krzysztof |
author_facet | Grzesiak, Jakub Śmieszek, Agnieszka Marycz, Krzysztof |
author_sort | Grzesiak, Jakub |
collection | PubMed |
description | BACKGROUND: Osteogenic differentiation of mesenchymal stem cells has been extensively investigated with regards to different aspects, including the analysis of cell intracellular and extracellular proteome, cell gene expression pattern, and morphology. During the osteogenic differentiation, osteoblasts produce and release specific proteins, like osteocalcin and osteopontin. Simultaneously, cells produce the extracellular matrix (ECM) that resembles the bone ECM, with high quantity of calcium and phosphorus. We focused on the ultrastructural changes occurring during the osteogenic differentiation of MSC cultured in alginate hydrogel. RESULTS: The analysis revealed that during the osteogenic differentiation the most of cells become dead, and these dead cells contain large quantities of calcium and deposition is strictly connected with the cellular death and small membrane vesicles released by cells. Cell organelles were not present within differentiated cells, while in cells from non-osteogenic group the cellular ultrastructure was proper, with single nuclei, endoplasmic reticulum and numerous mitochondria. CONCLUSION: The ECM synthesis and deposition during the osteogenic differentiation of MSC involves cellular programmed death. The small membrane vesicles become the mineralization sites of formed bone ECM. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13578-016-0128-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5210287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52102872017-01-06 Ultrastructural changes during osteogenic differentiation in mesenchymal stromal cells cultured in alginate hydrogel Grzesiak, Jakub Śmieszek, Agnieszka Marycz, Krzysztof Cell Biosci Research BACKGROUND: Osteogenic differentiation of mesenchymal stem cells has been extensively investigated with regards to different aspects, including the analysis of cell intracellular and extracellular proteome, cell gene expression pattern, and morphology. During the osteogenic differentiation, osteoblasts produce and release specific proteins, like osteocalcin and osteopontin. Simultaneously, cells produce the extracellular matrix (ECM) that resembles the bone ECM, with high quantity of calcium and phosphorus. We focused on the ultrastructural changes occurring during the osteogenic differentiation of MSC cultured in alginate hydrogel. RESULTS: The analysis revealed that during the osteogenic differentiation the most of cells become dead, and these dead cells contain large quantities of calcium and deposition is strictly connected with the cellular death and small membrane vesicles released by cells. Cell organelles were not present within differentiated cells, while in cells from non-osteogenic group the cellular ultrastructure was proper, with single nuclei, endoplasmic reticulum and numerous mitochondria. CONCLUSION: The ECM synthesis and deposition during the osteogenic differentiation of MSC involves cellular programmed death. The small membrane vesicles become the mineralization sites of formed bone ECM. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13578-016-0128-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-03 /pmc/articles/PMC5210287/ /pubmed/28066541 http://dx.doi.org/10.1186/s13578-016-0128-0 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Grzesiak, Jakub Śmieszek, Agnieszka Marycz, Krzysztof Ultrastructural changes during osteogenic differentiation in mesenchymal stromal cells cultured in alginate hydrogel |
title | Ultrastructural changes during osteogenic differentiation in mesenchymal stromal cells cultured in alginate hydrogel |
title_full | Ultrastructural changes during osteogenic differentiation in mesenchymal stromal cells cultured in alginate hydrogel |
title_fullStr | Ultrastructural changes during osteogenic differentiation in mesenchymal stromal cells cultured in alginate hydrogel |
title_full_unstemmed | Ultrastructural changes during osteogenic differentiation in mesenchymal stromal cells cultured in alginate hydrogel |
title_short | Ultrastructural changes during osteogenic differentiation in mesenchymal stromal cells cultured in alginate hydrogel |
title_sort | ultrastructural changes during osteogenic differentiation in mesenchymal stromal cells cultured in alginate hydrogel |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210287/ https://www.ncbi.nlm.nih.gov/pubmed/28066541 http://dx.doi.org/10.1186/s13578-016-0128-0 |
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