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Modulating the Electrical and Mechanical Microenvironment to Guide Neuronal Stem Cell Differentiation
The application of induced pluripotent stem cells (iPSCs) in disease modeling and regenerative medicine can be limited by the prolonged times required for functional human neuronal differentiation and traditional 2D culture techniques. Here, a conductive graphene scaffold (CGS) to modulate mechanica...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025039/ https://www.ncbi.nlm.nih.gov/pubmed/33854874 http://dx.doi.org/10.1002/advs.202002112 |
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author | Oh, Byeongtaek Wu, Yu‐Wei Swaminathan, Vishal Lam, Vivek Ding, Jun George, Paul M. |
author_facet | Oh, Byeongtaek Wu, Yu‐Wei Swaminathan, Vishal Lam, Vivek Ding, Jun George, Paul M. |
author_sort | Oh, Byeongtaek |
collection | PubMed |
description | The application of induced pluripotent stem cells (iPSCs) in disease modeling and regenerative medicine can be limited by the prolonged times required for functional human neuronal differentiation and traditional 2D culture techniques. Here, a conductive graphene scaffold (CGS) to modulate mechanical and electrical signals to promote human iPSC‐derived neurons is presented. The soft CGS with cortex‐like stiffness (≈3 kPa) and electrical stimulation (±800 mV/100 Hz for 1 h) incurs a fivefold improvement in the rate (14d) of generating iPSC‐derived neurons over some traditional protocols, with an increase in mature cellular markers and electrophysiological characteristics. Consistent with other culture conditions, it is found that the pro‐neurogenic effects of mechanical and electrical stimuli rely on RhoA/ROCK signaling and de novo ciliary neurotrophic factor (CNTF) production respectively. Thus, the CGS system creates a combined physical and continuously modifiable, electrical niche to efficiently and quickly generate iPSC‐derived neurons. |
format | Online Article Text |
id | pubmed-8025039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80250392021-04-13 Modulating the Electrical and Mechanical Microenvironment to Guide Neuronal Stem Cell Differentiation Oh, Byeongtaek Wu, Yu‐Wei Swaminathan, Vishal Lam, Vivek Ding, Jun George, Paul M. Adv Sci (Weinh) Full Papers The application of induced pluripotent stem cells (iPSCs) in disease modeling and regenerative medicine can be limited by the prolonged times required for functional human neuronal differentiation and traditional 2D culture techniques. Here, a conductive graphene scaffold (CGS) to modulate mechanical and electrical signals to promote human iPSC‐derived neurons is presented. The soft CGS with cortex‐like stiffness (≈3 kPa) and electrical stimulation (±800 mV/100 Hz for 1 h) incurs a fivefold improvement in the rate (14d) of generating iPSC‐derived neurons over some traditional protocols, with an increase in mature cellular markers and electrophysiological characteristics. Consistent with other culture conditions, it is found that the pro‐neurogenic effects of mechanical and electrical stimuli rely on RhoA/ROCK signaling and de novo ciliary neurotrophic factor (CNTF) production respectively. Thus, the CGS system creates a combined physical and continuously modifiable, electrical niche to efficiently and quickly generate iPSC‐derived neurons. John Wiley and Sons Inc. 2021-02-18 /pmc/articles/PMC8025039/ /pubmed/33854874 http://dx.doi.org/10.1002/advs.202002112 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Oh, Byeongtaek Wu, Yu‐Wei Swaminathan, Vishal Lam, Vivek Ding, Jun George, Paul M. Modulating the Electrical and Mechanical Microenvironment to Guide Neuronal Stem Cell Differentiation |
title | Modulating the Electrical and Mechanical Microenvironment to Guide Neuronal Stem Cell Differentiation |
title_full | Modulating the Electrical and Mechanical Microenvironment to Guide Neuronal Stem Cell Differentiation |
title_fullStr | Modulating the Electrical and Mechanical Microenvironment to Guide Neuronal Stem Cell Differentiation |
title_full_unstemmed | Modulating the Electrical and Mechanical Microenvironment to Guide Neuronal Stem Cell Differentiation |
title_short | Modulating the Electrical and Mechanical Microenvironment to Guide Neuronal Stem Cell Differentiation |
title_sort | modulating the electrical and mechanical microenvironment to guide neuronal stem cell differentiation |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025039/ https://www.ncbi.nlm.nih.gov/pubmed/33854874 http://dx.doi.org/10.1002/advs.202002112 |
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