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Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function

A bioengineered skeletal muscle construct that mimics structural and functional characteristics of native skeletal muscle is a promising therapeutic option to treat extensive muscle defect injuries. We previously showed that bioprinted human skeletal muscle constructs were able to form multi-layered...

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Autores principales: Kim, Ji Hyun, Kim, Ickhee, Seol, Young-Joon, Ko, In Kap, Yoo, James J., Atala, Anthony, Lee, Sang Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039897/
https://www.ncbi.nlm.nih.gov/pubmed/32094341
http://dx.doi.org/10.1038/s41467-020-14930-9
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author Kim, Ji Hyun
Kim, Ickhee
Seol, Young-Joon
Ko, In Kap
Yoo, James J.
Atala, Anthony
Lee, Sang Jin
author_facet Kim, Ji Hyun
Kim, Ickhee
Seol, Young-Joon
Ko, In Kap
Yoo, James J.
Atala, Anthony
Lee, Sang Jin
author_sort Kim, Ji Hyun
collection PubMed
description A bioengineered skeletal muscle construct that mimics structural and functional characteristics of native skeletal muscle is a promising therapeutic option to treat extensive muscle defect injuries. We previously showed that bioprinted human skeletal muscle constructs were able to form multi-layered bundles with aligned myofibers. In this study, we investigate the effects of neural cell integration into the bioprinted skeletal muscle construct to accelerate functional muscle regeneration in vivo. Neural input into this bioprinted skeletal muscle construct shows the improvement of myofiber formation, long-term survival, and neuromuscular junction formation in vitro. More importantly, the bioprinted constructs with neural cell integration facilitate rapid innervation and mature into organized muscle tissue that restores normal muscle weight and function in a rodent model of muscle defect injury. These results suggest that the 3D bioprinted human neural-skeletal muscle constructs can be rapidly integrated with the host neural network, resulting in accelerated muscle function restoration.
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spelling pubmed-70398972020-03-04 Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function Kim, Ji Hyun Kim, Ickhee Seol, Young-Joon Ko, In Kap Yoo, James J. Atala, Anthony Lee, Sang Jin Nat Commun Article A bioengineered skeletal muscle construct that mimics structural and functional characteristics of native skeletal muscle is a promising therapeutic option to treat extensive muscle defect injuries. We previously showed that bioprinted human skeletal muscle constructs were able to form multi-layered bundles with aligned myofibers. In this study, we investigate the effects of neural cell integration into the bioprinted skeletal muscle construct to accelerate functional muscle regeneration in vivo. Neural input into this bioprinted skeletal muscle construct shows the improvement of myofiber formation, long-term survival, and neuromuscular junction formation in vitro. More importantly, the bioprinted constructs with neural cell integration facilitate rapid innervation and mature into organized muscle tissue that restores normal muscle weight and function in a rodent model of muscle defect injury. These results suggest that the 3D bioprinted human neural-skeletal muscle constructs can be rapidly integrated with the host neural network, resulting in accelerated muscle function restoration. Nature Publishing Group UK 2020-02-24 /pmc/articles/PMC7039897/ /pubmed/32094341 http://dx.doi.org/10.1038/s41467-020-14930-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Ji Hyun
Kim, Ickhee
Seol, Young-Joon
Ko, In Kap
Yoo, James J.
Atala, Anthony
Lee, Sang Jin
Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function
title Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function
title_full Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function
title_fullStr Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function
title_full_unstemmed Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function
title_short Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function
title_sort neural cell integration into 3d bioprinted skeletal muscle constructs accelerates restoration of muscle function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039897/
https://www.ncbi.nlm.nih.gov/pubmed/32094341
http://dx.doi.org/10.1038/s41467-020-14930-9
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