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Fabrication of scaffold-free tubular cardiac constructs using a Bio-3D printer

A major challenge in cardiac tissue engineering is the host’s immune response to artificial materials. To overcome this problem, we established a scaffold-free system for assembling cell constructs using an automated Bio-3D printer. This printer has previously been used to fabricate other three-dime...

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Autores principales: Arai, Kenichi, Murata, Daiki, Verissimo, Ana Raquel, Mukae, Yosuke, Itoh, Manabu, Nakamura, Anna, Morita, Shigeki, Nakayama, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296519/
https://www.ncbi.nlm.nih.gov/pubmed/30557409
http://dx.doi.org/10.1371/journal.pone.0209162
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author Arai, Kenichi
Murata, Daiki
Verissimo, Ana Raquel
Mukae, Yosuke
Itoh, Manabu
Nakamura, Anna
Morita, Shigeki
Nakayama, Koichi
author_facet Arai, Kenichi
Murata, Daiki
Verissimo, Ana Raquel
Mukae, Yosuke
Itoh, Manabu
Nakamura, Anna
Morita, Shigeki
Nakayama, Koichi
author_sort Arai, Kenichi
collection PubMed
description A major challenge in cardiac tissue engineering is the host’s immune response to artificial materials. To overcome this problem, we established a scaffold-free system for assembling cell constructs using an automated Bio-3D printer. This printer has previously been used to fabricate other three-dimensional (3D) constructs, including liver, blood vessels, and cartilage. In the present study, we tested the function in vivo of scaffold-free cardiac tubular construct fabricated using this system. Cardiomyocytes derived from induced pluripotent stem cells (iCells), endothelial cells, and fibroblasts were combined to make the spheroids. Subsequently, tubular cardiac constructs were fabricated by Bio-3D printer placing the spheroids on a needle array. Notably, the spheroid fusion and beat rate in the constructs were observed while still on the needle array. After removal from the needle array, electrical stimulation was used to test responsiveness of the constructs. An increased beat rate was observed during stimulation. Importantly, the constructs returned to their initial beat rate after stimulation was stopped. In addition, histological analysis shows cellular reorganization occurring in the cardiac constructs, which may mimic that observed during organ transplantation. Taken together, our results indicate that these engineered cardiac tubular constructs, which address both the limited supply of donor tissues as well as the immune-induced transplant rejection, has potential to be used for both clinical and drug testing applications. To our knowledge, this is the first time that cardiac tubular constructs have been produced using optimized Bio-3D printing technique and subsequently tested for their use as cardiac pumps.
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spelling pubmed-62965192018-12-28 Fabrication of scaffold-free tubular cardiac constructs using a Bio-3D printer Arai, Kenichi Murata, Daiki Verissimo, Ana Raquel Mukae, Yosuke Itoh, Manabu Nakamura, Anna Morita, Shigeki Nakayama, Koichi PLoS One Research Article A major challenge in cardiac tissue engineering is the host’s immune response to artificial materials. To overcome this problem, we established a scaffold-free system for assembling cell constructs using an automated Bio-3D printer. This printer has previously been used to fabricate other three-dimensional (3D) constructs, including liver, blood vessels, and cartilage. In the present study, we tested the function in vivo of scaffold-free cardiac tubular construct fabricated using this system. Cardiomyocytes derived from induced pluripotent stem cells (iCells), endothelial cells, and fibroblasts were combined to make the spheroids. Subsequently, tubular cardiac constructs were fabricated by Bio-3D printer placing the spheroids on a needle array. Notably, the spheroid fusion and beat rate in the constructs were observed while still on the needle array. After removal from the needle array, electrical stimulation was used to test responsiveness of the constructs. An increased beat rate was observed during stimulation. Importantly, the constructs returned to their initial beat rate after stimulation was stopped. In addition, histological analysis shows cellular reorganization occurring in the cardiac constructs, which may mimic that observed during organ transplantation. Taken together, our results indicate that these engineered cardiac tubular constructs, which address both the limited supply of donor tissues as well as the immune-induced transplant rejection, has potential to be used for both clinical and drug testing applications. To our knowledge, this is the first time that cardiac tubular constructs have been produced using optimized Bio-3D printing technique and subsequently tested for their use as cardiac pumps. Public Library of Science 2018-12-17 /pmc/articles/PMC6296519/ /pubmed/30557409 http://dx.doi.org/10.1371/journal.pone.0209162 Text en © 2018 Arai 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
Arai, Kenichi
Murata, Daiki
Verissimo, Ana Raquel
Mukae, Yosuke
Itoh, Manabu
Nakamura, Anna
Morita, Shigeki
Nakayama, Koichi
Fabrication of scaffold-free tubular cardiac constructs using a Bio-3D printer
title Fabrication of scaffold-free tubular cardiac constructs using a Bio-3D printer
title_full Fabrication of scaffold-free tubular cardiac constructs using a Bio-3D printer
title_fullStr Fabrication of scaffold-free tubular cardiac constructs using a Bio-3D printer
title_full_unstemmed Fabrication of scaffold-free tubular cardiac constructs using a Bio-3D printer
title_short Fabrication of scaffold-free tubular cardiac constructs using a Bio-3D printer
title_sort fabrication of scaffold-free tubular cardiac constructs using a bio-3d printer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296519/
https://www.ncbi.nlm.nih.gov/pubmed/30557409
http://dx.doi.org/10.1371/journal.pone.0209162
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