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Osteoclastogenic Potential of Tissue-Engineered Periosteal Sheet: Effects of Culture Media on the Ability to Recruit Osteoclast Precursors

Cell culture media influence the characteristics of human osteogenic periosteal sheets. We have previously found that a stem cell medium facilitates growth and collagen matrix formation in vitro and osteogenesis in vivo. However, it has not yet been demonstrated which culture medium is superior for...

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Autores principales: Uematsu, Kohya, Ushiki, Takashi, Ishiguro, Hajime, Ohashi, Riuko, Tamura, Suguru, Watanabe, Mari, Fujimoto, Yoko, Nagata, Masaki, Ajioka, Yoichi, Kawase, Tomoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926432/
https://www.ncbi.nlm.nih.gov/pubmed/33671612
http://dx.doi.org/10.3390/ijms22042169
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author Uematsu, Kohya
Ushiki, Takashi
Ishiguro, Hajime
Ohashi, Riuko
Tamura, Suguru
Watanabe, Mari
Fujimoto, Yoko
Nagata, Masaki
Ajioka, Yoichi
Kawase, Tomoyuki
author_facet Uematsu, Kohya
Ushiki, Takashi
Ishiguro, Hajime
Ohashi, Riuko
Tamura, Suguru
Watanabe, Mari
Fujimoto, Yoko
Nagata, Masaki
Ajioka, Yoichi
Kawase, Tomoyuki
author_sort Uematsu, Kohya
collection PubMed
description Cell culture media influence the characteristics of human osteogenic periosteal sheets. We have previously found that a stem cell medium facilitates growth and collagen matrix formation in vitro and osteogenesis in vivo. However, it has not yet been demonstrated which culture medium is superior for osteoclastogenesis, a prerequisite for reconstruction of normal bone metabolic basis. To address this question, we compared chemotaxis and osteoclastogenesis in tissue-engineered periosteal sheets (TPSs) prepared with two types of culture media. Periosteal tissues obtained from adult volunteers were expanded with the conventional Medium 199 or with the stem cell medium, MesenPRO. Hematopoietic enhanced-green-fluorescent-protein (EGFP)-nude mice were prepared by γ-irradiation of Balb/c nu/nu mice and subsequent transplantation of bone marrow cells from CAG-EGFP C57BL/6 mice. TPSs were implanted subcutaneously into the chimeric mice and retrieved after intervals for immunohistopathological examination. EGFP(+) cells were similarly recruited to the implantation site in both the TPSs prepared, whereas the distribution of CD11b(+) cells was significantly lower in the TPS prepared with the stem cell medium. Instead, osteoclastogenesis was higher in the TPS prepared with the stem cell medium than in the one prepared with the conventional medium. These findings suggest that the stem cell medium is preferable for the preparation of more functional TPSs.
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spelling pubmed-79264322021-03-04 Osteoclastogenic Potential of Tissue-Engineered Periosteal Sheet: Effects of Culture Media on the Ability to Recruit Osteoclast Precursors Uematsu, Kohya Ushiki, Takashi Ishiguro, Hajime Ohashi, Riuko Tamura, Suguru Watanabe, Mari Fujimoto, Yoko Nagata, Masaki Ajioka, Yoichi Kawase, Tomoyuki Int J Mol Sci Article Cell culture media influence the characteristics of human osteogenic periosteal sheets. We have previously found that a stem cell medium facilitates growth and collagen matrix formation in vitro and osteogenesis in vivo. However, it has not yet been demonstrated which culture medium is superior for osteoclastogenesis, a prerequisite for reconstruction of normal bone metabolic basis. To address this question, we compared chemotaxis and osteoclastogenesis in tissue-engineered periosteal sheets (TPSs) prepared with two types of culture media. Periosteal tissues obtained from adult volunteers were expanded with the conventional Medium 199 or with the stem cell medium, MesenPRO. Hematopoietic enhanced-green-fluorescent-protein (EGFP)-nude mice were prepared by γ-irradiation of Balb/c nu/nu mice and subsequent transplantation of bone marrow cells from CAG-EGFP C57BL/6 mice. TPSs were implanted subcutaneously into the chimeric mice and retrieved after intervals for immunohistopathological examination. EGFP(+) cells were similarly recruited to the implantation site in both the TPSs prepared, whereas the distribution of CD11b(+) cells was significantly lower in the TPS prepared with the stem cell medium. Instead, osteoclastogenesis was higher in the TPS prepared with the stem cell medium than in the one prepared with the conventional medium. These findings suggest that the stem cell medium is preferable for the preparation of more functional TPSs. MDPI 2021-02-22 /pmc/articles/PMC7926432/ /pubmed/33671612 http://dx.doi.org/10.3390/ijms22042169 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Uematsu, Kohya
Ushiki, Takashi
Ishiguro, Hajime
Ohashi, Riuko
Tamura, Suguru
Watanabe, Mari
Fujimoto, Yoko
Nagata, Masaki
Ajioka, Yoichi
Kawase, Tomoyuki
Osteoclastogenic Potential of Tissue-Engineered Periosteal Sheet: Effects of Culture Media on the Ability to Recruit Osteoclast Precursors
title Osteoclastogenic Potential of Tissue-Engineered Periosteal Sheet: Effects of Culture Media on the Ability to Recruit Osteoclast Precursors
title_full Osteoclastogenic Potential of Tissue-Engineered Periosteal Sheet: Effects of Culture Media on the Ability to Recruit Osteoclast Precursors
title_fullStr Osteoclastogenic Potential of Tissue-Engineered Periosteal Sheet: Effects of Culture Media on the Ability to Recruit Osteoclast Precursors
title_full_unstemmed Osteoclastogenic Potential of Tissue-Engineered Periosteal Sheet: Effects of Culture Media on the Ability to Recruit Osteoclast Precursors
title_short Osteoclastogenic Potential of Tissue-Engineered Periosteal Sheet: Effects of Culture Media on the Ability to Recruit Osteoclast Precursors
title_sort osteoclastogenic potential of tissue-engineered periosteal sheet: effects of culture media on the ability to recruit osteoclast precursors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926432/
https://www.ncbi.nlm.nih.gov/pubmed/33671612
http://dx.doi.org/10.3390/ijms22042169
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