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Biomimetic mineralization using matrix vesicle nanofragments

In vitro synthesis of bone tissue has been paid attention in recent years; however, current methods to fabricate bone tissue are still ineffective due to some remaining gaps in the understanding of real in vivo bone formation process, and application of the knowledge in bone synthesis. Therefore, th...

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Autores principales: Kunitomi, Yosuke, Hara, Emilio Satoshi, Okada, Masahiro, Nagaoka, Noriyuki, Kuboki, Takuo, Nakano, Takayoshi, Kamioka, Hiroshi, Matsumoto, Takuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594056/
https://www.ncbi.nlm.nih.gov/pubmed/30675987
http://dx.doi.org/10.1002/jbm.a.36618
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author Kunitomi, Yosuke
Hara, Emilio Satoshi
Okada, Masahiro
Nagaoka, Noriyuki
Kuboki, Takuo
Nakano, Takayoshi
Kamioka, Hiroshi
Matsumoto, Takuya
author_facet Kunitomi, Yosuke
Hara, Emilio Satoshi
Okada, Masahiro
Nagaoka, Noriyuki
Kuboki, Takuo
Nakano, Takayoshi
Kamioka, Hiroshi
Matsumoto, Takuya
author_sort Kunitomi, Yosuke
collection PubMed
description In vitro synthesis of bone tissue has been paid attention in recent years; however, current methods to fabricate bone tissue are still ineffective due to some remaining gaps in the understanding of real in vivo bone formation process, and application of the knowledge in bone synthesis. Therefore, the objectives of this study were first, to perform a systematic and ultrastructural investigation of the initial mineral formation during intramembranous ossification of mouse calvaria from a material scientists' viewpoint, and to develop novel mineralization methods based on the in vivo findings. First, the very initial mineral deposition was found to occur at embryonic day E14.0 in mouse calvaria. Analysis of the initial bone formation process showed that it involved the following distinct steps: collagen secretion, matrix vesicle (MV) release, MV mineralization, MV rupture, and collagen fiber mineralization. Next, we performed in vitro mineralization experiments using MVs and hydrogel scaffolds. Intact MVs embedded in collagen gel did not mineralize, whereas, interestingly, MV nanofragments obtained by ultrasonication could promote rapid mineralization. These results indicate that mechanically ruptured MV membrane can be a promising material for in vitro bone tissue synthesis. © 2019 The Authors. journal Of Biomedical Materials Research Part A Published By Wiley Periodicals, Inc. J Biomed Mater Res Part A: 107A: 1021–1030, 2019.
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spelling pubmed-65940562019-07-10 Biomimetic mineralization using matrix vesicle nanofragments Kunitomi, Yosuke Hara, Emilio Satoshi Okada, Masahiro Nagaoka, Noriyuki Kuboki, Takuo Nakano, Takayoshi Kamioka, Hiroshi Matsumoto, Takuya J Biomed Mater Res A Original Articles In vitro synthesis of bone tissue has been paid attention in recent years; however, current methods to fabricate bone tissue are still ineffective due to some remaining gaps in the understanding of real in vivo bone formation process, and application of the knowledge in bone synthesis. Therefore, the objectives of this study were first, to perform a systematic and ultrastructural investigation of the initial mineral formation during intramembranous ossification of mouse calvaria from a material scientists' viewpoint, and to develop novel mineralization methods based on the in vivo findings. First, the very initial mineral deposition was found to occur at embryonic day E14.0 in mouse calvaria. Analysis of the initial bone formation process showed that it involved the following distinct steps: collagen secretion, matrix vesicle (MV) release, MV mineralization, MV rupture, and collagen fiber mineralization. Next, we performed in vitro mineralization experiments using MVs and hydrogel scaffolds. Intact MVs embedded in collagen gel did not mineralize, whereas, interestingly, MV nanofragments obtained by ultrasonication could promote rapid mineralization. These results indicate that mechanically ruptured MV membrane can be a promising material for in vitro bone tissue synthesis. © 2019 The Authors. journal Of Biomedical Materials Research Part A Published By Wiley Periodicals, Inc. J Biomed Mater Res Part A: 107A: 1021–1030, 2019. John Wiley & Sons, Inc. 2019-02-11 2019-05 /pmc/articles/PMC6594056/ /pubmed/30675987 http://dx.doi.org/10.1002/jbm.a.36618 Text en © 2019 The Authors. Journal of Biomedical Materials Research Part A published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Kunitomi, Yosuke
Hara, Emilio Satoshi
Okada, Masahiro
Nagaoka, Noriyuki
Kuboki, Takuo
Nakano, Takayoshi
Kamioka, Hiroshi
Matsumoto, Takuya
Biomimetic mineralization using matrix vesicle nanofragments
title Biomimetic mineralization using matrix vesicle nanofragments
title_full Biomimetic mineralization using matrix vesicle nanofragments
title_fullStr Biomimetic mineralization using matrix vesicle nanofragments
title_full_unstemmed Biomimetic mineralization using matrix vesicle nanofragments
title_short Biomimetic mineralization using matrix vesicle nanofragments
title_sort biomimetic mineralization using matrix vesicle nanofragments
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594056/
https://www.ncbi.nlm.nih.gov/pubmed/30675987
http://dx.doi.org/10.1002/jbm.a.36618
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