Papers

Peer-reviewed Last author Corresponding author International journal
May, 2019

Biomimetic mineralization using matrix vesicle nanofragments.

Journal of biomedical materials research. Part A
  • Yosuke Kunitomi
  • ,
  • Emilio Satoshi Hara
  • ,
  • Masahiro Okada
  • ,
  • Noriyuki Nagaoka
  • ,
  • Takuo Kuboki
  • ,
  • Takayoshi Nakano
  • ,
  • Hiroshi Kamioka
  • ,
  • Takuya Matsumoto

Volume
107
Number
5
First page
1021
Last page
1030
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1002/jbm.a.36618

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.

Link information
DOI
https://doi.org/10.1002/jbm.a.36618
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30675987
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594056
ID information
  • DOI : 10.1002/jbm.a.36618
  • ISSN : 1549-3296
  • Pubmed ID : 30675987
  • Pubmed Central ID : PMC6594056

Export
BibTeX RIS