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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...

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Autores principales: Oh, Byeongtaek, Wu, Yu‐Wei, Swaminathan, Vishal, Lam, Vivek, Ding, Jun, George, Paul M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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