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Passage number affects differentiation of sensory neurons from human induced pluripotent stem cells

Induced pluripotent stem cells (iPSCs) are a valuable resource for neurological disease-modeling and drug discovery due to their ability to differentiate into neurons reflecting the genetics of the patient from which they are derived. iPSC-derived cultures, however, are highly variable due to hetero...

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Autores principales: Cantor, Erica L., Shen, Fei, Jiang, Guanglong, Tan, Zhiyong, Cunningham, Geneva M., Wu, Xi, Philips, Santosh, Schneider, Bryan P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508090/
https://www.ncbi.nlm.nih.gov/pubmed/36151116
http://dx.doi.org/10.1038/s41598-022-19018-6
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author Cantor, Erica L.
Shen, Fei
Jiang, Guanglong
Tan, Zhiyong
Cunningham, Geneva M.
Wu, Xi
Philips, Santosh
Schneider, Bryan P.
author_facet Cantor, Erica L.
Shen, Fei
Jiang, Guanglong
Tan, Zhiyong
Cunningham, Geneva M.
Wu, Xi
Philips, Santosh
Schneider, Bryan P.
author_sort Cantor, Erica L.
collection PubMed
description Induced pluripotent stem cells (iPSCs) are a valuable resource for neurological disease-modeling and drug discovery due to their ability to differentiate into neurons reflecting the genetics of the patient from which they are derived. iPSC-derived cultures, however, are highly variable due to heterogeneity in culture conditions. We investigated the effect of passage number on iPSC differentiation to optimize the generation of sensory neurons (iPSC-dSNs). Three iPSC lines reprogrammed from the peripheral blood of three donors were differentiated into iPSC-dSNs at passage numbers within each of the following ranges: low (5–10), intermediate (20–26), and high (30–38). Morphology and pluripotency of the parent iPSCs were assessed prior to differentiation. iPSC-dSNs were evaluated based on electrophysiological properties and expression of key neuronal markers. All iPSC lines displayed similar morphology and were similarly pluripotent across passage numbers. However, the expression levels of neuronal markers and sodium channel function analyses indicated that iPSC-dSNs differentiated from low passage numbers better recapitulated the sensory neuron phenotype than those differentiated from intermediate or high passage numbers. Our results demonstrate that lower passage numbers may be better suited for differentiation into peripheral sensory neurons.
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spelling pubmed-95080902022-09-25 Passage number affects differentiation of sensory neurons from human induced pluripotent stem cells Cantor, Erica L. Shen, Fei Jiang, Guanglong Tan, Zhiyong Cunningham, Geneva M. Wu, Xi Philips, Santosh Schneider, Bryan P. Sci Rep Article Induced pluripotent stem cells (iPSCs) are a valuable resource for neurological disease-modeling and drug discovery due to their ability to differentiate into neurons reflecting the genetics of the patient from which they are derived. iPSC-derived cultures, however, are highly variable due to heterogeneity in culture conditions. We investigated the effect of passage number on iPSC differentiation to optimize the generation of sensory neurons (iPSC-dSNs). Three iPSC lines reprogrammed from the peripheral blood of three donors were differentiated into iPSC-dSNs at passage numbers within each of the following ranges: low (5–10), intermediate (20–26), and high (30–38). Morphology and pluripotency of the parent iPSCs were assessed prior to differentiation. iPSC-dSNs were evaluated based on electrophysiological properties and expression of key neuronal markers. All iPSC lines displayed similar morphology and were similarly pluripotent across passage numbers. However, the expression levels of neuronal markers and sodium channel function analyses indicated that iPSC-dSNs differentiated from low passage numbers better recapitulated the sensory neuron phenotype than those differentiated from intermediate or high passage numbers. Our results demonstrate that lower passage numbers may be better suited for differentiation into peripheral sensory neurons. Nature Publishing Group UK 2022-09-23 /pmc/articles/PMC9508090/ /pubmed/36151116 http://dx.doi.org/10.1038/s41598-022-19018-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Cantor, Erica L.
Shen, Fei
Jiang, Guanglong
Tan, Zhiyong
Cunningham, Geneva M.
Wu, Xi
Philips, Santosh
Schneider, Bryan P.
Passage number affects differentiation of sensory neurons from human induced pluripotent stem cells
title Passage number affects differentiation of sensory neurons from human induced pluripotent stem cells
title_full Passage number affects differentiation of sensory neurons from human induced pluripotent stem cells
title_fullStr Passage number affects differentiation of sensory neurons from human induced pluripotent stem cells
title_full_unstemmed Passage number affects differentiation of sensory neurons from human induced pluripotent stem cells
title_short Passage number affects differentiation of sensory neurons from human induced pluripotent stem cells
title_sort passage number affects differentiation of sensory neurons from human induced pluripotent stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508090/
https://www.ncbi.nlm.nih.gov/pubmed/36151116
http://dx.doi.org/10.1038/s41598-022-19018-6
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