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Application of stem-cell media to explant culture of human periosteum: An optimal approach for preparing osteogenic cell material
As part of our clinical tests on bone regeneration using cultured periosteal sheets, here, we prepared cultured periosteal sheets in two types of stem-cell culture media, STK1 and STK3. Human periosteum was expanded either in 1% human serum–supplemented STK1 for 28 days, in 1% human serum–supplement...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927863/ https://www.ncbi.nlm.nih.gov/pubmed/24555010 http://dx.doi.org/10.1177/2041731413509646 |
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author | Uematsu, Kohya Nagata, Masaki Kawase, Tomoyuki Suzuki, Kenji Takagi, Ritsuo |
author_facet | Uematsu, Kohya Nagata, Masaki Kawase, Tomoyuki Suzuki, Kenji Takagi, Ritsuo |
author_sort | Uematsu, Kohya |
collection | PubMed |
description | As part of our clinical tests on bone regeneration using cultured periosteal sheets, here, we prepared cultured periosteal sheets in two types of stem-cell culture media, STK1 and STK3. Human periosteum was expanded either in 1% human serum–supplemented STK1 for 28 days, in 1% human serum–supplemented STK1 for 14 days followed by 1% human serum–supplemented STK3 for 14 days (1% human serum–supplemented STK1+3), or in 10% fetal bovine serum–supplemented Medium 199 for 28 days (control). Cultured periosteal sheet diameter and DNA content were significantly higher, and the multilayer structure was prominent in 1% human serum–supplemented STK1 and 1% human serum–supplemented STK1+3. The messenger RNA of osteoblastic markers was significantly upregulated in 1% human serum–supplemented STK1+3. Osteopontin-immunopositive staining and mineralization were evident across a wide area of the cultured periosteal sheet in 1% human serum–supplemented STK1+3. Subcutaneous implantation in nude mice following expansion in 1% human serum–supplemented STK1+3 produced the highest cultured periosteal sheet osteogenic activity. Expansion in 1% human serum–supplemented STK1+3 successfully induced cultured periosteal sheet growth while retaining osteogenic potential, and subsequent osteoblastic induction promoted the production of homogeneous cell material. |
format | Online Article Text |
id | pubmed-3927863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-39278632014-02-19 Application of stem-cell media to explant culture of human periosteum: An optimal approach for preparing osteogenic cell material Uematsu, Kohya Nagata, Masaki Kawase, Tomoyuki Suzuki, Kenji Takagi, Ritsuo J Tissue Eng Article As part of our clinical tests on bone regeneration using cultured periosteal sheets, here, we prepared cultured periosteal sheets in two types of stem-cell culture media, STK1 and STK3. Human periosteum was expanded either in 1% human serum–supplemented STK1 for 28 days, in 1% human serum–supplemented STK1 for 14 days followed by 1% human serum–supplemented STK3 for 14 days (1% human serum–supplemented STK1+3), or in 10% fetal bovine serum–supplemented Medium 199 for 28 days (control). Cultured periosteal sheet diameter and DNA content were significantly higher, and the multilayer structure was prominent in 1% human serum–supplemented STK1 and 1% human serum–supplemented STK1+3. The messenger RNA of osteoblastic markers was significantly upregulated in 1% human serum–supplemented STK1+3. Osteopontin-immunopositive staining and mineralization were evident across a wide area of the cultured periosteal sheet in 1% human serum–supplemented STK1+3. Subcutaneous implantation in nude mice following expansion in 1% human serum–supplemented STK1+3 produced the highest cultured periosteal sheet osteogenic activity. Expansion in 1% human serum–supplemented STK1+3 successfully induced cultured periosteal sheet growth while retaining osteogenic potential, and subsequent osteoblastic induction promoted the production of homogeneous cell material. SAGE Publications 2013-10-23 /pmc/articles/PMC3927863/ /pubmed/24555010 http://dx.doi.org/10.1177/2041731413509646 Text en © The Author(s) 2013 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(http://www.uk.sagepub.com/aboutus/openaccess.htm). |
spellingShingle | Article Uematsu, Kohya Nagata, Masaki Kawase, Tomoyuki Suzuki, Kenji Takagi, Ritsuo Application of stem-cell media to explant culture of human periosteum: An optimal approach for preparing osteogenic cell material |
title | Application of stem-cell media to explant culture of human periosteum: An optimal approach for preparing osteogenic cell material |
title_full | Application of stem-cell media to explant culture of human periosteum: An optimal approach for preparing osteogenic cell material |
title_fullStr | Application of stem-cell media to explant culture of human periosteum: An optimal approach for preparing osteogenic cell material |
title_full_unstemmed | Application of stem-cell media to explant culture of human periosteum: An optimal approach for preparing osteogenic cell material |
title_short | Application of stem-cell media to explant culture of human periosteum: An optimal approach for preparing osteogenic cell material |
title_sort | application of stem-cell media to explant culture of human periosteum: an optimal approach for preparing osteogenic cell material |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927863/ https://www.ncbi.nlm.nih.gov/pubmed/24555010 http://dx.doi.org/10.1177/2041731413509646 |
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