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Bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology
BACKGROUND: Human dental pulp stem cells (DPSCs), which have the ability to differentiate into multiple lineages, were recently identified. DPSCs can be collected readily from extracted teeth and are now considered to be a type of mesenchymal stem cell with higher clonogenic and proliferative potent...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796442/ https://www.ncbi.nlm.nih.gov/pubmed/29391049 http://dx.doi.org/10.1186/s13287-018-0783-7 |
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author | Fujii, Yasuyuki Kawase-Koga, Yoko Hojo, Hironori Yano, Fumiko Sato, Marika Chung, Ung-il Ohba, Shinsuke Chikazu, Daichi |
author_facet | Fujii, Yasuyuki Kawase-Koga, Yoko Hojo, Hironori Yano, Fumiko Sato, Marika Chung, Ung-il Ohba, Shinsuke Chikazu, Daichi |
author_sort | Fujii, Yasuyuki |
collection | PubMed |
description | BACKGROUND: Human dental pulp stem cells (DPSCs), which have the ability to differentiate into multiple lineages, were recently identified. DPSCs can be collected readily from extracted teeth and are now considered to be a type of mesenchymal stem cell with higher clonogenic and proliferative potential than bone marrow stem cells (BMSCs). Meanwhile, the treatment of severe bone defects, such as fractures, cancers, and congenital abnormalities, remains a great challenge, and novel bone regenerative techniques are highly anticipated. Several studies have previously shown that 4-(4-methoxyphenyl)pyrido[40,30:4,5]thieno[2,3-b]pyridine-2-carboxamide (TH), a helioxanthin derivative, induces osteogenic differentiation of preosteoblastic and mesenchymal cells. However, the osteogenic differentiation activities of TH have only been confirmed in some mouse cell lines. Therefore, in this study, toward the clinical use of TH in humans, we analyzed the effect of TH on the osteogenic differentiation of DPSCs, and the in-vivo osteogenesis ability of TH-induced DPSCs, taking advantage of the simple transplantation system using cell-sheet technology. METHODS: DPSCs were obtained from dental pulp of the wisdom teeth of five healthy patients (18–22 years old) and cultured in regular medium and osteogenic medium with or without TH. To evaluate osteogenesis of TH-induced DPSCs in vivo, we transplanted DPSC sheets into mouse calvaria defects. RESULTS: We demonstrated that osteogenic conditions with TH induce the osteogenic differentiation of DPSCs more efficiently than those without TH and those with bone morphogenetic protein-2. However, regular medium with TH did not induce the osteogenic differentiation of DPSCs. TH induced osteogenesis in both DPSCs and BMSCs, although the gene expression pattern in DPSCs differed from that in BMSCs up to 14 days after induction with TH. Furthermore, we succeeded in bone regeneration in vivo using DPSC sheets with TH treatment, without using any scaffolds or growth factors. CONCLUSIONS: Our results demonstrate that TH-induced DPSCs are a useful cell source for bone regenerative medicine, and the transplantation of DPSC sheets treated with TH is a convenient scaffold-free method of bone healing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0783-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5796442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57964422018-02-12 Bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology Fujii, Yasuyuki Kawase-Koga, Yoko Hojo, Hironori Yano, Fumiko Sato, Marika Chung, Ung-il Ohba, Shinsuke Chikazu, Daichi Stem Cell Res Ther Research BACKGROUND: Human dental pulp stem cells (DPSCs), which have the ability to differentiate into multiple lineages, were recently identified. DPSCs can be collected readily from extracted teeth and are now considered to be a type of mesenchymal stem cell with higher clonogenic and proliferative potential than bone marrow stem cells (BMSCs). Meanwhile, the treatment of severe bone defects, such as fractures, cancers, and congenital abnormalities, remains a great challenge, and novel bone regenerative techniques are highly anticipated. Several studies have previously shown that 4-(4-methoxyphenyl)pyrido[40,30:4,5]thieno[2,3-b]pyridine-2-carboxamide (TH), a helioxanthin derivative, induces osteogenic differentiation of preosteoblastic and mesenchymal cells. However, the osteogenic differentiation activities of TH have only been confirmed in some mouse cell lines. Therefore, in this study, toward the clinical use of TH in humans, we analyzed the effect of TH on the osteogenic differentiation of DPSCs, and the in-vivo osteogenesis ability of TH-induced DPSCs, taking advantage of the simple transplantation system using cell-sheet technology. METHODS: DPSCs were obtained from dental pulp of the wisdom teeth of five healthy patients (18–22 years old) and cultured in regular medium and osteogenic medium with or without TH. To evaluate osteogenesis of TH-induced DPSCs in vivo, we transplanted DPSC sheets into mouse calvaria defects. RESULTS: We demonstrated that osteogenic conditions with TH induce the osteogenic differentiation of DPSCs more efficiently than those without TH and those with bone morphogenetic protein-2. However, regular medium with TH did not induce the osteogenic differentiation of DPSCs. TH induced osteogenesis in both DPSCs and BMSCs, although the gene expression pattern in DPSCs differed from that in BMSCs up to 14 days after induction with TH. Furthermore, we succeeded in bone regeneration in vivo using DPSC sheets with TH treatment, without using any scaffolds or growth factors. CONCLUSIONS: Our results demonstrate that TH-induced DPSCs are a useful cell source for bone regenerative medicine, and the transplantation of DPSC sheets treated with TH is a convenient scaffold-free method of bone healing. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0783-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-01 /pmc/articles/PMC5796442/ /pubmed/29391049 http://dx.doi.org/10.1186/s13287-018-0783-7 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Fujii, Yasuyuki Kawase-Koga, Yoko Hojo, Hironori Yano, Fumiko Sato, Marika Chung, Ung-il Ohba, Shinsuke Chikazu, Daichi Bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology |
title | Bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology |
title_full | Bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology |
title_fullStr | Bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology |
title_full_unstemmed | Bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology |
title_short | Bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology |
title_sort | bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796442/ https://www.ncbi.nlm.nih.gov/pubmed/29391049 http://dx.doi.org/10.1186/s13287-018-0783-7 |
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