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Controlling properties of human neural progenitor cells using 2D and 3D conductive polymer scaffolds
Human induced pluripotent stem cell-derived neural progenitor cells (hNPCs) are a promising cell source for stem cell transplantation to treat neurological diseases such as stroke and peripheral nerve injuries. However, there have been limited studies investigating how the dimensionality of the phys...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925212/ https://www.ncbi.nlm.nih.gov/pubmed/31863072 http://dx.doi.org/10.1038/s41598-019-56021-w |
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author | Song, Shang Amores, Danielle Chen, Cheng McConnell, Kelly Oh, Byeongtaek Poon, Ada George, Paul M. |
author_facet | Song, Shang Amores, Danielle Chen, Cheng McConnell, Kelly Oh, Byeongtaek Poon, Ada George, Paul M. |
author_sort | Song, Shang |
collection | PubMed |
description | Human induced pluripotent stem cell-derived neural progenitor cells (hNPCs) are a promising cell source for stem cell transplantation to treat neurological diseases such as stroke and peripheral nerve injuries. However, there have been limited studies investigating how the dimensionality of the physical and electrical microenvironment affects hNPC function. In this study, we report the fabrication of two- and three-dimensional (2D and 3D respectively) constructs composed of a conductive polymer to compare the effect of electrical stimulation of hydrogel-immobilized hNPCs. The physical dimension (2D vs 3D) of stimulating platforms alone changed the hNPCs gene expression related to cell proliferation and metabolic pathways. The addition of electrical stimulation was critical in upregulating gene expression of neurotrophic factors that are important in regulating cell survival, synaptic remodeling, and nerve regeneration. This study demonstrates that the applied electrical field controls hNPC properties depending on the physical nature of stimulating platforms and cellular metabolic states. The ability to control hNPC functions can be beneficial in understanding mechanistic changes related to electrical modulation and devising novel treatment methods for neurological diseases. |
format | Online Article Text |
id | pubmed-6925212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69252122019-12-24 Controlling properties of human neural progenitor cells using 2D and 3D conductive polymer scaffolds Song, Shang Amores, Danielle Chen, Cheng McConnell, Kelly Oh, Byeongtaek Poon, Ada George, Paul M. Sci Rep Article Human induced pluripotent stem cell-derived neural progenitor cells (hNPCs) are a promising cell source for stem cell transplantation to treat neurological diseases such as stroke and peripheral nerve injuries. However, there have been limited studies investigating how the dimensionality of the physical and electrical microenvironment affects hNPC function. In this study, we report the fabrication of two- and three-dimensional (2D and 3D respectively) constructs composed of a conductive polymer to compare the effect of electrical stimulation of hydrogel-immobilized hNPCs. The physical dimension (2D vs 3D) of stimulating platforms alone changed the hNPCs gene expression related to cell proliferation and metabolic pathways. The addition of electrical stimulation was critical in upregulating gene expression of neurotrophic factors that are important in regulating cell survival, synaptic remodeling, and nerve regeneration. This study demonstrates that the applied electrical field controls hNPC properties depending on the physical nature of stimulating platforms and cellular metabolic states. The ability to control hNPC functions can be beneficial in understanding mechanistic changes related to electrical modulation and devising novel treatment methods for neurological diseases. Nature Publishing Group UK 2019-12-20 /pmc/articles/PMC6925212/ /pubmed/31863072 http://dx.doi.org/10.1038/s41598-019-56021-w Text en © The Author(s) 2019 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/. |
spellingShingle | Article Song, Shang Amores, Danielle Chen, Cheng McConnell, Kelly Oh, Byeongtaek Poon, Ada George, Paul M. Controlling properties of human neural progenitor cells using 2D and 3D conductive polymer scaffolds |
title | Controlling properties of human neural progenitor cells using 2D and 3D conductive polymer scaffolds |
title_full | Controlling properties of human neural progenitor cells using 2D and 3D conductive polymer scaffolds |
title_fullStr | Controlling properties of human neural progenitor cells using 2D and 3D conductive polymer scaffolds |
title_full_unstemmed | Controlling properties of human neural progenitor cells using 2D and 3D conductive polymer scaffolds |
title_short | Controlling properties of human neural progenitor cells using 2D and 3D conductive polymer scaffolds |
title_sort | controlling properties of human neural progenitor cells using 2d and 3d conductive polymer scaffolds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925212/ https://www.ncbi.nlm.nih.gov/pubmed/31863072 http://dx.doi.org/10.1038/s41598-019-56021-w |
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