Cargando…
Bio-artificial bone formation model with a radial-flow bioreactor for implant therapy—comparison between two cell culture carriers: porous hydroxyapatite and β-tricalcium phosphate beads
Bone grafting is necessary before dental implant treatment in patients with jaw bone defects. Currently, autologous bone grafting is a major burden on the patient. However, it is impossible to form a sufficient foundation for the implant with a bone-filling agent alone. It is, therefore, necessary t...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315002/ https://www.ncbi.nlm.nih.gov/pubmed/30276761 http://dx.doi.org/10.1007/s13577-018-0218-x |
_version_ | 1783384186917224448 |
---|---|
author | Nomoto, Hideki Maehashi, Haruka Shirai, Misako Nakamura, Mariko Masaki, Takahiro Mezaki, Yoshihiro Park, Jonghyuk Aizawa, Mamoru Ohkawa, Kiyoshi Yoshida, Kiyotsugu Matsuura, Tomokazu |
author_facet | Nomoto, Hideki Maehashi, Haruka Shirai, Misako Nakamura, Mariko Masaki, Takahiro Mezaki, Yoshihiro Park, Jonghyuk Aizawa, Mamoru Ohkawa, Kiyoshi Yoshida, Kiyotsugu Matsuura, Tomokazu |
author_sort | Nomoto, Hideki |
collection | PubMed |
description | Bone grafting is necessary before dental implant treatment in patients with jaw bone defects. Currently, autologous bone grafting is a major burden on the patient. However, it is impossible to form a sufficient foundation for the implant with a bone-filling agent alone. It is, therefore, necessary to prepare hybrid artificial bone tissue containing osteoblasts and osteoclasts. In this study, mouse MC3T3-E1 pre-osteoblast cells and human embryonic-derived osteoblastic cell line hFOB1.19 were cultured in radial-flow bioreactors (RFB) to form three-dimensional artificial bone filled with porous beads of β-tricalcium phosphate (β-TCP) or hydroxyapatite (HA)—which are clinically used as bone-filling agents—as cell culture carriers. When circulation culturing was performed in the growth medium for the first 10–12 days, glucose consumption was increased in the cultures with HA beads in comparison to the cultures with β-TCP beads. When cultured in the differentiation culture medium during the second half of the culture period, the glucose consumption decreased in the culture with HA beads. A DNA microarray analysis suggested that osteogenesis progressed fast in three-dimensional culture filled with HA beads and that partly differentiation into osteoblasts was prominent in cultures with β-TCP beads. In the growth process of MC3T3-E1 cells, the vitamin A metabolism was also activated, the synthesis and degradation of retinoic acid was enhanced, and the metabolism of the same process decreased at the end of differentiation in three-dimensional cultures. Three-dimensional circulation culture in RFB is considered to be useful for the formation of hybrid bio-artificial bone tissue. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13577-018-0218-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6315002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-63150022019-01-11 Bio-artificial bone formation model with a radial-flow bioreactor for implant therapy—comparison between two cell culture carriers: porous hydroxyapatite and β-tricalcium phosphate beads Nomoto, Hideki Maehashi, Haruka Shirai, Misako Nakamura, Mariko Masaki, Takahiro Mezaki, Yoshihiro Park, Jonghyuk Aizawa, Mamoru Ohkawa, Kiyoshi Yoshida, Kiyotsugu Matsuura, Tomokazu Hum Cell Research Article Bone grafting is necessary before dental implant treatment in patients with jaw bone defects. Currently, autologous bone grafting is a major burden on the patient. However, it is impossible to form a sufficient foundation for the implant with a bone-filling agent alone. It is, therefore, necessary to prepare hybrid artificial bone tissue containing osteoblasts and osteoclasts. In this study, mouse MC3T3-E1 pre-osteoblast cells and human embryonic-derived osteoblastic cell line hFOB1.19 were cultured in radial-flow bioreactors (RFB) to form three-dimensional artificial bone filled with porous beads of β-tricalcium phosphate (β-TCP) or hydroxyapatite (HA)—which are clinically used as bone-filling agents—as cell culture carriers. When circulation culturing was performed in the growth medium for the first 10–12 days, glucose consumption was increased in the cultures with HA beads in comparison to the cultures with β-TCP beads. When cultured in the differentiation culture medium during the second half of the culture period, the glucose consumption decreased in the culture with HA beads. A DNA microarray analysis suggested that osteogenesis progressed fast in three-dimensional culture filled with HA beads and that partly differentiation into osteoblasts was prominent in cultures with β-TCP beads. In the growth process of MC3T3-E1 cells, the vitamin A metabolism was also activated, the synthesis and degradation of retinoic acid was enhanced, and the metabolism of the same process decreased at the end of differentiation in three-dimensional cultures. Three-dimensional circulation culture in RFB is considered to be useful for the formation of hybrid bio-artificial bone tissue. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13577-018-0218-x) contains supplementary material, which is available to authorized users. Springer Japan 2018-10-01 2019 /pmc/articles/PMC6315002/ /pubmed/30276761 http://dx.doi.org/10.1007/s13577-018-0218-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Article Nomoto, Hideki Maehashi, Haruka Shirai, Misako Nakamura, Mariko Masaki, Takahiro Mezaki, Yoshihiro Park, Jonghyuk Aizawa, Mamoru Ohkawa, Kiyoshi Yoshida, Kiyotsugu Matsuura, Tomokazu Bio-artificial bone formation model with a radial-flow bioreactor for implant therapy—comparison between two cell culture carriers: porous hydroxyapatite and β-tricalcium phosphate beads |
title | Bio-artificial bone formation model with a radial-flow bioreactor for implant therapy—comparison between two cell culture carriers: porous hydroxyapatite and β-tricalcium phosphate beads |
title_full | Bio-artificial bone formation model with a radial-flow bioreactor for implant therapy—comparison between two cell culture carriers: porous hydroxyapatite and β-tricalcium phosphate beads |
title_fullStr | Bio-artificial bone formation model with a radial-flow bioreactor for implant therapy—comparison between two cell culture carriers: porous hydroxyapatite and β-tricalcium phosphate beads |
title_full_unstemmed | Bio-artificial bone formation model with a radial-flow bioreactor for implant therapy—comparison between two cell culture carriers: porous hydroxyapatite and β-tricalcium phosphate beads |
title_short | Bio-artificial bone formation model with a radial-flow bioreactor for implant therapy—comparison between two cell culture carriers: porous hydroxyapatite and β-tricalcium phosphate beads |
title_sort | bio-artificial bone formation model with a radial-flow bioreactor for implant therapy—comparison between two cell culture carriers: porous hydroxyapatite and β-tricalcium phosphate beads |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315002/ https://www.ncbi.nlm.nih.gov/pubmed/30276761 http://dx.doi.org/10.1007/s13577-018-0218-x |
work_keys_str_mv | AT nomotohideki bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT maehashiharuka bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT shiraimisako bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT nakamuramariko bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT masakitakahiro bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT mezakiyoshihiro bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT parkjonghyuk bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT aizawamamoru bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT ohkawakiyoshi bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT yoshidakiyotsugu bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads AT matsuuratomokazu bioartificialboneformationmodelwitharadialflowbioreactorforimplanttherapycomparisonbetweentwocellculturecarriersporoushydroxyapatiteandbtricalciumphosphatebeads |