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A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells

A computer-designed, solvent-free scaffold offer several potential advantages such as ease of customized manufacture and in vivo safety. In this work, we firstly used a computer-designed, solvent-free scaffold and human dental pulp stem cells (hDPSCs) to regenerate neo-bone within cranial bone defec...

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Autores principales: Yeon Kwon, Doo, Seon Kwon, Jin, Hun Park, Seung, Hun Park, Ji, Hee Jang, So, Yun Yin, Xiang, Yun, Jeong-Ho, Ho Kim, Jae, Hyun Min, Byoung, Hee Lee, Jun, Kim, Wan-Doo, Suk Kim, Moon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522608/
https://www.ncbi.nlm.nih.gov/pubmed/26234712
http://dx.doi.org/10.1038/srep12721
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author Yeon Kwon, Doo
Seon Kwon, Jin
Hun Park, Seung
Hun Park, Ji
Hee Jang, So
Yun Yin, Xiang
Yun, Jeong-Ho
Ho Kim, Jae
Hyun Min, Byoung
Hee Lee, Jun
Kim, Wan-Doo
Suk Kim, Moon
author_facet Yeon Kwon, Doo
Seon Kwon, Jin
Hun Park, Seung
Hun Park, Ji
Hee Jang, So
Yun Yin, Xiang
Yun, Jeong-Ho
Ho Kim, Jae
Hyun Min, Byoung
Hee Lee, Jun
Kim, Wan-Doo
Suk Kim, Moon
author_sort Yeon Kwon, Doo
collection PubMed
description A computer-designed, solvent-free scaffold offer several potential advantages such as ease of customized manufacture and in vivo safety. In this work, we firstly used a computer-designed, solvent-free scaffold and human dental pulp stem cells (hDPSCs) to regenerate neo-bone within cranial bone defects. The hDPSCs expressed mesenchymal stem cell markers and served as an abundant source of stem cells with a high proliferation rate. In addition, hDPSCs showed a phenotype of differentiated osteoblasts in the presence of osteogenic factors (OF). We used solid freeform fabrication (SFF) with biodegradable polyesters (MPEG-(PLLA-co-PGA-co-PCL) (PLGC)) to fabricate a computer-designed scaffold. The SFF technology gave quick and reproducible results. To assess bone tissue engineering in vivo, the computer-designed, circular PLGC scaffold was implanted into a full-thickness cranial bone defect and monitored by micro-computed tomography (CT) and histology of the in vivo tissue-engineered bone. Neo-bone formation of more than 50% in both micro-CT and histology tests was observed at only PLGC scaffold with hDPSCs/OF. Furthermore, the PLGC scaffold gradually degraded, as evidenced by the fluorescent-labeled PLGC scaffold, which provides information to tract biodegradation of implanted PLGC scaffold. In conclusion, we confirmed neo-bone formation within a cranial bone defect using hDPSCs and a computer-designed PLGC scaffold.
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spelling pubmed-45226082015-08-06 A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells Yeon Kwon, Doo Seon Kwon, Jin Hun Park, Seung Hun Park, Ji Hee Jang, So Yun Yin, Xiang Yun, Jeong-Ho Ho Kim, Jae Hyun Min, Byoung Hee Lee, Jun Kim, Wan-Doo Suk Kim, Moon Sci Rep Article A computer-designed, solvent-free scaffold offer several potential advantages such as ease of customized manufacture and in vivo safety. In this work, we firstly used a computer-designed, solvent-free scaffold and human dental pulp stem cells (hDPSCs) to regenerate neo-bone within cranial bone defects. The hDPSCs expressed mesenchymal stem cell markers and served as an abundant source of stem cells with a high proliferation rate. In addition, hDPSCs showed a phenotype of differentiated osteoblasts in the presence of osteogenic factors (OF). We used solid freeform fabrication (SFF) with biodegradable polyesters (MPEG-(PLLA-co-PGA-co-PCL) (PLGC)) to fabricate a computer-designed scaffold. The SFF technology gave quick and reproducible results. To assess bone tissue engineering in vivo, the computer-designed, circular PLGC scaffold was implanted into a full-thickness cranial bone defect and monitored by micro-computed tomography (CT) and histology of the in vivo tissue-engineered bone. Neo-bone formation of more than 50% in both micro-CT and histology tests was observed at only PLGC scaffold with hDPSCs/OF. Furthermore, the PLGC scaffold gradually degraded, as evidenced by the fluorescent-labeled PLGC scaffold, which provides information to tract biodegradation of implanted PLGC scaffold. In conclusion, we confirmed neo-bone formation within a cranial bone defect using hDPSCs and a computer-designed PLGC scaffold. Nature Publishing Group 2015-08-03 /pmc/articles/PMC4522608/ /pubmed/26234712 http://dx.doi.org/10.1038/srep12721 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yeon Kwon, Doo
Seon Kwon, Jin
Hun Park, Seung
Hun Park, Ji
Hee Jang, So
Yun Yin, Xiang
Yun, Jeong-Ho
Ho Kim, Jae
Hyun Min, Byoung
Hee Lee, Jun
Kim, Wan-Doo
Suk Kim, Moon
A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells
title A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells
title_full A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells
title_fullStr A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells
title_full_unstemmed A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells
title_short A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells
title_sort computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522608/
https://www.ncbi.nlm.nih.gov/pubmed/26234712
http://dx.doi.org/10.1038/srep12721
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