TY - JOUR
T1 - Biomimetic mineralization using matrix vesicle nanofragments
AU - Kunitomi, Yosuke
AU - Hara, Emilio Satoshi
AU - Okada, Masahiro
AU - Nagaoka, Noriyuki
AU - Kuboki, Takuo
AU - Nakano, Takayoshi
AU - Kamioka, Hiroshi
AU - Matsumoto, Takuya
N1 - Funding Information:
Additional Supporting Information may be found in the online version of this article. †These authors contributed equally to this work. Correspondence to: Takuya Matsumoto; e-mail: tmatsu@md.okayama-u.ac.jp Contract grant sponsor: JSPS KAKENHI; contract grant number: JP18H05254 and JP25220912 and JP16H05533 and JP16H06990 and JP18K17119 This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 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.
Funding Information:
This study was supported by JSPS KAKENHI Grant Number (JP18K17119, JP16H06990, JP16H05533, JP25220912, and JP18H05254).
Publisher Copyright:
© 2019 The Authors. Journal of Biomedical Materials Research Part A published by Wiley Periodicals, Inc.
PY - 2019/5
Y1 - 2019/5
N2 - 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.
AB - 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.
KW - apatite
KW - bioinspired mineralization
KW - bone
KW - hydrogel
KW - matrix vesicle nanofragments
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U2 - 10.1002/jbm.a.36618
DO - 10.1002/jbm.a.36618
M3 - Article
C2 - 30675987
AN - SCOPUS:85061453442
SN - 1549-3296
VL - 107
SP - 1021
EP - 1030
JO - Journal of Biomedical Materials Research - Part A
JF - Journal of Biomedical Materials Research - Part A
IS - 5
ER -