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Generation of cortical neurons through large-scale expanding neuroepithelial stem cell from human pluripotent stem cells
BACKGROUND: Considerable progress has been made in converting human pluripotent stem cells (hPSCs) into cortical neurons for disease modeling and regenerative medicine. However, these procedures are hard to provide sufficient cells for their applications. Using a combination of small-molecules and g...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532602/ https://www.ncbi.nlm.nih.gov/pubmed/33008480 http://dx.doi.org/10.1186/s13287-020-01939-6 |
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author | Zhao, Shumei Duan, Kui Ai, Zongyong Niu, Baohua Chen, Yanying Kong, Ruize Li, Tianqing |
author_facet | Zhao, Shumei Duan, Kui Ai, Zongyong Niu, Baohua Chen, Yanying Kong, Ruize Li, Tianqing |
author_sort | Zhao, Shumei |
collection | PubMed |
description | BACKGROUND: Considerable progress has been made in converting human pluripotent stem cells (hPSCs) into cortical neurons for disease modeling and regenerative medicine. However, these procedures are hard to provide sufficient cells for their applications. Using a combination of small-molecules and growth factors, we previously identified one condition which can rapidly induce hPSCs into neuroepithelial stem cells (NESCs). Here, we developed a scalable suspension culture system, which largely yields high-quality NESC-spheres and subsequent cortical neurons. METHODS: The NESC medium was first optimized, and the suspension culture system was then enlarged from plates to stirred bioreactors for large-scale production of NESC-spheres by a stirring speed of 60 rpm. During the expansion, the quality of NESC-spheres was evaluated. The differentiation potential of NESC-spheres into cortical neurons was demonstrated by removing bFGF and two pathway inhibitors from the NESC medium. Cellular immunofluorescence staining, global transcriptome, and single-cell RNA sequencing analysis were used to identify the characteristics, identities, purities, or homogeneities of NESC-spheres or their differentiated cells, respectively. RESULTS: The optimized culture system is more conducive to large-scale suspension production of NESCs. These largely expanded NESC-spheres maintain unlimited self-renewal ability and NESC state by retaining their uniform sizes, high cell vitalities, and robust expansion abilities. After long-term expansion, NESC-spheres preserve high purity, homogeneity, and normal diploid karyotype. These expanded NESC-spheres on a large scale have strong differentiation potential and effectively produce mature cortical neurons. CONCLUSIONS: We developed a serum-free, defined, and low-cost culture system for large-scale expansion of NESCs in stirred suspension bioreactors. The stable and controllable 3D system supports long-term expansion of high-quality and homogeneous NESC-spheres. These NESC-spheres can be used to efficiently give rise to cortical neurons for cell therapy, disease modeling, and drug screening in future. |
format | Online Article Text |
id | pubmed-7532602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75326022020-10-05 Generation of cortical neurons through large-scale expanding neuroepithelial stem cell from human pluripotent stem cells Zhao, Shumei Duan, Kui Ai, Zongyong Niu, Baohua Chen, Yanying Kong, Ruize Li, Tianqing Stem Cell Res Ther Research BACKGROUND: Considerable progress has been made in converting human pluripotent stem cells (hPSCs) into cortical neurons for disease modeling and regenerative medicine. However, these procedures are hard to provide sufficient cells for their applications. Using a combination of small-molecules and growth factors, we previously identified one condition which can rapidly induce hPSCs into neuroepithelial stem cells (NESCs). Here, we developed a scalable suspension culture system, which largely yields high-quality NESC-spheres and subsequent cortical neurons. METHODS: The NESC medium was first optimized, and the suspension culture system was then enlarged from plates to stirred bioreactors for large-scale production of NESC-spheres by a stirring speed of 60 rpm. During the expansion, the quality of NESC-spheres was evaluated. The differentiation potential of NESC-spheres into cortical neurons was demonstrated by removing bFGF and two pathway inhibitors from the NESC medium. Cellular immunofluorescence staining, global transcriptome, and single-cell RNA sequencing analysis were used to identify the characteristics, identities, purities, or homogeneities of NESC-spheres or their differentiated cells, respectively. RESULTS: The optimized culture system is more conducive to large-scale suspension production of NESCs. These largely expanded NESC-spheres maintain unlimited self-renewal ability and NESC state by retaining their uniform sizes, high cell vitalities, and robust expansion abilities. After long-term expansion, NESC-spheres preserve high purity, homogeneity, and normal diploid karyotype. These expanded NESC-spheres on a large scale have strong differentiation potential and effectively produce mature cortical neurons. CONCLUSIONS: We developed a serum-free, defined, and low-cost culture system for large-scale expansion of NESCs in stirred suspension bioreactors. The stable and controllable 3D system supports long-term expansion of high-quality and homogeneous NESC-spheres. These NESC-spheres can be used to efficiently give rise to cortical neurons for cell therapy, disease modeling, and drug screening in future. BioMed Central 2020-10-02 /pmc/articles/PMC7532602/ /pubmed/33008480 http://dx.doi.org/10.1186/s13287-020-01939-6 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhao, Shumei Duan, Kui Ai, Zongyong Niu, Baohua Chen, Yanying Kong, Ruize Li, Tianqing Generation of cortical neurons through large-scale expanding neuroepithelial stem cell from human pluripotent stem cells |
title | Generation of cortical neurons through large-scale expanding neuroepithelial stem cell from human pluripotent stem cells |
title_full | Generation of cortical neurons through large-scale expanding neuroepithelial stem cell from human pluripotent stem cells |
title_fullStr | Generation of cortical neurons through large-scale expanding neuroepithelial stem cell from human pluripotent stem cells |
title_full_unstemmed | Generation of cortical neurons through large-scale expanding neuroepithelial stem cell from human pluripotent stem cells |
title_short | Generation of cortical neurons through large-scale expanding neuroepithelial stem cell from human pluripotent stem cells |
title_sort | generation of cortical neurons through large-scale expanding neuroepithelial stem cell from human pluripotent stem cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532602/ https://www.ncbi.nlm.nih.gov/pubmed/33008480 http://dx.doi.org/10.1186/s13287-020-01939-6 |
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