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The one-step fabrication of porous hASC-laden GelMa constructs using a handheld printing system

The fabrication of highly porous cell-loaded structures in tissue engineering applications has been a challenging issue because non-porous cell-laden struts can cause severe cell necrosis in the middle region owing to poor transport of nutrients and oxygen. In this study, we propose a versatile hand...

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Autores principales: Jo, SeoYul, Lee, JiUn, Lee, Hyeongjin, Ryu, Dongryeol, Kim, GeunHyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257650/
https://www.ncbi.nlm.nih.gov/pubmed/37301902
http://dx.doi.org/10.1038/s41536-023-00307-1
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author Jo, SeoYul
Lee, JiUn
Lee, Hyeongjin
Ryu, Dongryeol
Kim, GeunHyung
author_facet Jo, SeoYul
Lee, JiUn
Lee, Hyeongjin
Ryu, Dongryeol
Kim, GeunHyung
author_sort Jo, SeoYul
collection PubMed
description The fabrication of highly porous cell-loaded structures in tissue engineering applications has been a challenging issue because non-porous cell-laden struts can cause severe cell necrosis in the middle region owing to poor transport of nutrients and oxygen. In this study, we propose a versatile handheld 3D printer for the effective fabrication of porous cell-laden methacrylated gelatin (GelMa) with high porosity (≈97%) by air injection and a bubble-making system using mesh filters through which a mixture of air/GelMa bioink is passed. In particular, the pore size and foamability of the cell constructs could be manipulated using various processing parameters (rheological properties of GelMa, filter size and number, and air-bioink volume ratio). To demonstrate the feasibility of the cell construct as a tissue engineering substitute for muscle regeneration, in vitro cellular activities and in vivo regeneration ability of human adipose stem cells were assessed. The in vitro results demonstrated that the human adipose stem cells (hASCs) fabricated using the handheld 3D printer were alive and well-proliferated. Furthermore, the in vivo results showed that the hASCs-constructs directly printed from the handheld 3D printer showed significant restoration of functionality and efficient muscle regeneration in the volumetric muscle loss model of mice. Based on these results, the fabrication method of the porous cell-laden construct could be a promising tool for regenerating muscle tissues.
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spelling pubmed-102576502023-06-12 The one-step fabrication of porous hASC-laden GelMa constructs using a handheld printing system Jo, SeoYul Lee, JiUn Lee, Hyeongjin Ryu, Dongryeol Kim, GeunHyung NPJ Regen Med Article The fabrication of highly porous cell-loaded structures in tissue engineering applications has been a challenging issue because non-porous cell-laden struts can cause severe cell necrosis in the middle region owing to poor transport of nutrients and oxygen. In this study, we propose a versatile handheld 3D printer for the effective fabrication of porous cell-laden methacrylated gelatin (GelMa) with high porosity (≈97%) by air injection and a bubble-making system using mesh filters through which a mixture of air/GelMa bioink is passed. In particular, the pore size and foamability of the cell constructs could be manipulated using various processing parameters (rheological properties of GelMa, filter size and number, and air-bioink volume ratio). To demonstrate the feasibility of the cell construct as a tissue engineering substitute for muscle regeneration, in vitro cellular activities and in vivo regeneration ability of human adipose stem cells were assessed. The in vitro results demonstrated that the human adipose stem cells (hASCs) fabricated using the handheld 3D printer were alive and well-proliferated. Furthermore, the in vivo results showed that the hASCs-constructs directly printed from the handheld 3D printer showed significant restoration of functionality and efficient muscle regeneration in the volumetric muscle loss model of mice. Based on these results, the fabrication method of the porous cell-laden construct could be a promising tool for regenerating muscle tissues. Nature Publishing Group UK 2023-06-10 /pmc/articles/PMC10257650/ /pubmed/37301902 http://dx.doi.org/10.1038/s41536-023-00307-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jo, SeoYul
Lee, JiUn
Lee, Hyeongjin
Ryu, Dongryeol
Kim, GeunHyung
The one-step fabrication of porous hASC-laden GelMa constructs using a handheld printing system
title The one-step fabrication of porous hASC-laden GelMa constructs using a handheld printing system
title_full The one-step fabrication of porous hASC-laden GelMa constructs using a handheld printing system
title_fullStr The one-step fabrication of porous hASC-laden GelMa constructs using a handheld printing system
title_full_unstemmed The one-step fabrication of porous hASC-laden GelMa constructs using a handheld printing system
title_short The one-step fabrication of porous hASC-laden GelMa constructs using a handheld printing system
title_sort one-step fabrication of porous hasc-laden gelma constructs using a handheld printing system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257650/
https://www.ncbi.nlm.nih.gov/pubmed/37301902
http://dx.doi.org/10.1038/s41536-023-00307-1
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