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Regeneration of esophagus using a scaffold-free biomimetic structure created with bio-three-dimensional printing
Various strategies have been attempted to replace esophageal defects with natural or artificial substitutes using tissue engineering. However, these methods have not yet reached clinical application because of the high risks related to their immunogenicity or insufficient biocompatibility. In this s...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408002/ https://www.ncbi.nlm.nih.gov/pubmed/30849123 http://dx.doi.org/10.1371/journal.pone.0211339 |
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author | Takeoka, Yosuke Matsumoto, Keitaro Taniguchi, Daisuke Tsuchiya, Tomoshi Machino, Ryusuke Moriyama, Masaaki Oyama, Shosaburo Tetsuo, Tomoyuki Taura, Yasuaki Takagi, Katsunori Yoshida, Takuya Elgalad, Abdelmotagaly Matsuo, Naoto Kunizaki, Masaki Tobinaga, Shuichi Nonaka, Takashi Hidaka, Shigekazu Yamasaki, Naoya Nakayama, Koichi Nagayasu, Takeshi |
author_facet | Takeoka, Yosuke Matsumoto, Keitaro Taniguchi, Daisuke Tsuchiya, Tomoshi Machino, Ryusuke Moriyama, Masaaki Oyama, Shosaburo Tetsuo, Tomoyuki Taura, Yasuaki Takagi, Katsunori Yoshida, Takuya Elgalad, Abdelmotagaly Matsuo, Naoto Kunizaki, Masaki Tobinaga, Shuichi Nonaka, Takashi Hidaka, Shigekazu Yamasaki, Naoya Nakayama, Koichi Nagayasu, Takeshi |
author_sort | Takeoka, Yosuke |
collection | PubMed |
description | Various strategies have been attempted to replace esophageal defects with natural or artificial substitutes using tissue engineering. However, these methods have not yet reached clinical application because of the high risks related to their immunogenicity or insufficient biocompatibility. In this study, we developed a scaffold-free structure with a mixture of cell types using bio-three-dimensional (3D) printing technology and assessed its characteristics in vitro and in vivo after transplantation into rats. Normal human dermal fibroblasts, human esophageal smooth muscle cells, human bone marrow-derived mesenchymal stem cells, and human umbilical vein endothelial cells were purchased and used as a cell source. After the preparation of multicellular spheroids, esophageal-like tube structures were prepared by bio-3D printing. The structures were matured in a bioreactor and transplanted into 10-12-week-old F344 male rats as esophageal grafts under general anesthesia. Mechanical and histochemical assessment of the structures were performed. Among 4 types of structures evaluated, those with the larger proportion of mesenchymal stem cells tended to show greater strength and expansion on mechanical testing and highly expressed α-smooth muscle actin and vascular endothelial growth factor on immunohistochemistry. Therefore, the structure with the larger proportion of mesenchymal stem cells was selected for transplantation. The scaffold-free structures had sufficient strength for transplantation between the esophagus and stomach using silicon stents. The structures were maintained in vivo for 30 days after transplantation. Smooth muscle cells were maintained, and flat epithelium extended and covered the inner surface of the lumen. Food had also passed through the structure. These results suggested that the esophagus-like scaffold-free tubular structures created using bio-3D printing could hold promise as a substitute for the repair of esophageal defects. |
format | Online Article Text |
id | pubmed-6408002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64080022019-03-17 Regeneration of esophagus using a scaffold-free biomimetic structure created with bio-three-dimensional printing Takeoka, Yosuke Matsumoto, Keitaro Taniguchi, Daisuke Tsuchiya, Tomoshi Machino, Ryusuke Moriyama, Masaaki Oyama, Shosaburo Tetsuo, Tomoyuki Taura, Yasuaki Takagi, Katsunori Yoshida, Takuya Elgalad, Abdelmotagaly Matsuo, Naoto Kunizaki, Masaki Tobinaga, Shuichi Nonaka, Takashi Hidaka, Shigekazu Yamasaki, Naoya Nakayama, Koichi Nagayasu, Takeshi PLoS One Research Article Various strategies have been attempted to replace esophageal defects with natural or artificial substitutes using tissue engineering. However, these methods have not yet reached clinical application because of the high risks related to their immunogenicity or insufficient biocompatibility. In this study, we developed a scaffold-free structure with a mixture of cell types using bio-three-dimensional (3D) printing technology and assessed its characteristics in vitro and in vivo after transplantation into rats. Normal human dermal fibroblasts, human esophageal smooth muscle cells, human bone marrow-derived mesenchymal stem cells, and human umbilical vein endothelial cells were purchased and used as a cell source. After the preparation of multicellular spheroids, esophageal-like tube structures were prepared by bio-3D printing. The structures were matured in a bioreactor and transplanted into 10-12-week-old F344 male rats as esophageal grafts under general anesthesia. Mechanical and histochemical assessment of the structures were performed. Among 4 types of structures evaluated, those with the larger proportion of mesenchymal stem cells tended to show greater strength and expansion on mechanical testing and highly expressed α-smooth muscle actin and vascular endothelial growth factor on immunohistochemistry. Therefore, the structure with the larger proportion of mesenchymal stem cells was selected for transplantation. The scaffold-free structures had sufficient strength for transplantation between the esophagus and stomach using silicon stents. The structures were maintained in vivo for 30 days after transplantation. Smooth muscle cells were maintained, and flat epithelium extended and covered the inner surface of the lumen. Food had also passed through the structure. These results suggested that the esophagus-like scaffold-free tubular structures created using bio-3D printing could hold promise as a substitute for the repair of esophageal defects. Public Library of Science 2019-03-08 /pmc/articles/PMC6408002/ /pubmed/30849123 http://dx.doi.org/10.1371/journal.pone.0211339 Text en © 2019 Takeoka et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Takeoka, Yosuke Matsumoto, Keitaro Taniguchi, Daisuke Tsuchiya, Tomoshi Machino, Ryusuke Moriyama, Masaaki Oyama, Shosaburo Tetsuo, Tomoyuki Taura, Yasuaki Takagi, Katsunori Yoshida, Takuya Elgalad, Abdelmotagaly Matsuo, Naoto Kunizaki, Masaki Tobinaga, Shuichi Nonaka, Takashi Hidaka, Shigekazu Yamasaki, Naoya Nakayama, Koichi Nagayasu, Takeshi Regeneration of esophagus using a scaffold-free biomimetic structure created with bio-three-dimensional printing |
title | Regeneration of esophagus using a scaffold-free biomimetic structure created with bio-three-dimensional printing |
title_full | Regeneration of esophagus using a scaffold-free biomimetic structure created with bio-three-dimensional printing |
title_fullStr | Regeneration of esophagus using a scaffold-free biomimetic structure created with bio-three-dimensional printing |
title_full_unstemmed | Regeneration of esophagus using a scaffold-free biomimetic structure created with bio-three-dimensional printing |
title_short | Regeneration of esophagus using a scaffold-free biomimetic structure created with bio-three-dimensional printing |
title_sort | regeneration of esophagus using a scaffold-free biomimetic structure created with bio-three-dimensional printing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408002/ https://www.ncbi.nlm.nih.gov/pubmed/30849123 http://dx.doi.org/10.1371/journal.pone.0211339 |
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