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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...

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Autores principales: Uematsu, Kohya, Nagata, Masaki, Kawase, Tomoyuki, Suzuki, Kenji, Takagi, Ritsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2013
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.
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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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