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3D bioprinting of conductive hydrogel for enhanced myogenic differentiation
Recently, hydrogels have gained enormous interest in three-dimensional (3D) bioprinting toward developing functional substitutes for tissue remolding. However, it is highly challenging to transmit electrical signals to cells due to the limited electrical conductivity of the bioprinted hydrogels. Her...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363764/ https://www.ncbi.nlm.nih.gov/pubmed/34408909 http://dx.doi.org/10.1093/rb/rbab035 |
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author | Wang, Ying Wang, Qingshuai Luo, Shengchang Chen, Zhoujiang Zheng, Xiang Kankala, Ranjith Kumar Chen, Aizheng Wang, Shibin |
author_facet | Wang, Ying Wang, Qingshuai Luo, Shengchang Chen, Zhoujiang Zheng, Xiang Kankala, Ranjith Kumar Chen, Aizheng Wang, Shibin |
author_sort | Wang, Ying |
collection | PubMed |
description | Recently, hydrogels have gained enormous interest in three-dimensional (3D) bioprinting toward developing functional substitutes for tissue remolding. However, it is highly challenging to transmit electrical signals to cells due to the limited electrical conductivity of the bioprinted hydrogels. Herein, we demonstrate the 3D bioprinting-assisted fabrication of a conductive hydrogel scaffold based on poly-3,4-ethylene dioxythiophene (PEDOT) nanoparticles (NPs) deposited in gelatin methacryloyl (GelMA) for enhanced myogenic differentiation of mouse myoblasts (C2C12 cells). Initially, PEDOT NPs are dispersed in the hydrogel uniformly to enhance the conductive property of the hydrogel scaffold. Notably, the incorporated PEDOT NPs showed minimal influence on the printing ability of GelMA. Then, C2C12 cells are successfully encapsulated within GelMA/PEDOT conductive hydrogels using 3D extrusion bioprinting. Furthermore, the proliferation, migration and differentiation efficacies of C2C12 cells in the highly conductive GelMA/PEDOT composite scaffolds are demonstrated using various in vitro investigations of live/dead staining, F-actin staining, desmin and myogenin immunofluorescence staining. Finally, the effects of electrical signals on the stimulation of the scaffolds are investigated toward the myogenic differentiation of C2C12 cells and the formation of myotubes in vitro. Collectively, our findings demonstrate that the fabrication of the conductive hydrogels provides a feasible approach for the encapsulation of cells and the regeneration of the muscle tissue. |
format | Online Article Text |
id | pubmed-8363764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83637642021-08-17 3D bioprinting of conductive hydrogel for enhanced myogenic differentiation Wang, Ying Wang, Qingshuai Luo, Shengchang Chen, Zhoujiang Zheng, Xiang Kankala, Ranjith Kumar Chen, Aizheng Wang, Shibin Regen Biomater Research Article Recently, hydrogels have gained enormous interest in three-dimensional (3D) bioprinting toward developing functional substitutes for tissue remolding. However, it is highly challenging to transmit electrical signals to cells due to the limited electrical conductivity of the bioprinted hydrogels. Herein, we demonstrate the 3D bioprinting-assisted fabrication of a conductive hydrogel scaffold based on poly-3,4-ethylene dioxythiophene (PEDOT) nanoparticles (NPs) deposited in gelatin methacryloyl (GelMA) for enhanced myogenic differentiation of mouse myoblasts (C2C12 cells). Initially, PEDOT NPs are dispersed in the hydrogel uniformly to enhance the conductive property of the hydrogel scaffold. Notably, the incorporated PEDOT NPs showed minimal influence on the printing ability of GelMA. Then, C2C12 cells are successfully encapsulated within GelMA/PEDOT conductive hydrogels using 3D extrusion bioprinting. Furthermore, the proliferation, migration and differentiation efficacies of C2C12 cells in the highly conductive GelMA/PEDOT composite scaffolds are demonstrated using various in vitro investigations of live/dead staining, F-actin staining, desmin and myogenin immunofluorescence staining. Finally, the effects of electrical signals on the stimulation of the scaffolds are investigated toward the myogenic differentiation of C2C12 cells and the formation of myotubes in vitro. Collectively, our findings demonstrate that the fabrication of the conductive hydrogels provides a feasible approach for the encapsulation of cells and the regeneration of the muscle tissue. Oxford University Press 2021-08-14 /pmc/articles/PMC8363764/ /pubmed/34408909 http://dx.doi.org/10.1093/rb/rbab035 Text en © The Author(s) 2021. Published by Oxford University Press. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Ying Wang, Qingshuai Luo, Shengchang Chen, Zhoujiang Zheng, Xiang Kankala, Ranjith Kumar Chen, Aizheng Wang, Shibin 3D bioprinting of conductive hydrogel for enhanced myogenic differentiation |
title | 3D bioprinting of conductive hydrogel for enhanced myogenic differentiation |
title_full | 3D bioprinting of conductive hydrogel for enhanced myogenic differentiation |
title_fullStr | 3D bioprinting of conductive hydrogel for enhanced myogenic differentiation |
title_full_unstemmed | 3D bioprinting of conductive hydrogel for enhanced myogenic differentiation |
title_short | 3D bioprinting of conductive hydrogel for enhanced myogenic differentiation |
title_sort | 3d bioprinting of conductive hydrogel for enhanced myogenic differentiation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363764/ https://www.ncbi.nlm.nih.gov/pubmed/34408909 http://dx.doi.org/10.1093/rb/rbab035 |
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