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Imaging-based chemical screening reveals activity-dependent neural differentiation of pluripotent stem cells
Mammalian pluripotent stem cells (PSCs) represent an important venue for understanding basic principles regulating tissue-specific differentiation and discovering new tools that may facilitate clinical applications. Mechanisms that direct neural differentiation of PSCs involve growth factor signalin...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771564/ https://www.ncbi.nlm.nih.gov/pubmed/24040509 http://dx.doi.org/10.7554/eLife.00508 |
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author | Sun, Yaping Dong, Zhiqiang Jin, Taihao Ang, Kean-Hooi Huang, Miller Haston, Kelly M Peng, Jisong Zhong, Tao P Finkbeiner, Steven Weiss, William A Arkin, Michelle R Jan, Lily Y Guo, Su |
author_facet | Sun, Yaping Dong, Zhiqiang Jin, Taihao Ang, Kean-Hooi Huang, Miller Haston, Kelly M Peng, Jisong Zhong, Tao P Finkbeiner, Steven Weiss, William A Arkin, Michelle R Jan, Lily Y Guo, Su |
author_sort | Sun, Yaping |
collection | PubMed |
description | Mammalian pluripotent stem cells (PSCs) represent an important venue for understanding basic principles regulating tissue-specific differentiation and discovering new tools that may facilitate clinical applications. Mechanisms that direct neural differentiation of PSCs involve growth factor signaling and transcription regulation. However, it is unknown whether and how electrical activity influences this process. Here we report a high throughput imaging-based screen, which uncovers that selamectin, an anti-helminthic therapeutic compound with reported activity on invertebrate glutamate-gated chloride channels, promotes neural differentiation of PSCs. We show that selamectin’s pro-neurogenic activity is mediated by γ2-containing GABA(A) receptors in subsets of neural rosette progenitors, accompanied by increased proneural and lineage-specific transcription factor expression and cell cycle exit. In vivo, selamectin promotes neurogenesis in developing zebrafish. Our results establish a chemical screening platform that reveals activity-dependent neural differentiation from PSCs. Compounds identified in this and future screening might prove therapeutically beneficial for treating neurodevelopmental or neurodegenerative disorders. DOI: http://dx.doi.org/10.7554/eLife.00508.001 |
format | Online Article Text |
id | pubmed-3771564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37715642013-09-13 Imaging-based chemical screening reveals activity-dependent neural differentiation of pluripotent stem cells Sun, Yaping Dong, Zhiqiang Jin, Taihao Ang, Kean-Hooi Huang, Miller Haston, Kelly M Peng, Jisong Zhong, Tao P Finkbeiner, Steven Weiss, William A Arkin, Michelle R Jan, Lily Y Guo, Su eLife Developmental Biology and Stem Cells Mammalian pluripotent stem cells (PSCs) represent an important venue for understanding basic principles regulating tissue-specific differentiation and discovering new tools that may facilitate clinical applications. Mechanisms that direct neural differentiation of PSCs involve growth factor signaling and transcription regulation. However, it is unknown whether and how electrical activity influences this process. Here we report a high throughput imaging-based screen, which uncovers that selamectin, an anti-helminthic therapeutic compound with reported activity on invertebrate glutamate-gated chloride channels, promotes neural differentiation of PSCs. We show that selamectin’s pro-neurogenic activity is mediated by γ2-containing GABA(A) receptors in subsets of neural rosette progenitors, accompanied by increased proneural and lineage-specific transcription factor expression and cell cycle exit. In vivo, selamectin promotes neurogenesis in developing zebrafish. Our results establish a chemical screening platform that reveals activity-dependent neural differentiation from PSCs. Compounds identified in this and future screening might prove therapeutically beneficial for treating neurodevelopmental or neurodegenerative disorders. DOI: http://dx.doi.org/10.7554/eLife.00508.001 eLife Sciences Publications, Ltd 2013-09-10 /pmc/articles/PMC3771564/ /pubmed/24040509 http://dx.doi.org/10.7554/eLife.00508 Text en Copyright © 2013, Sun et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells Sun, Yaping Dong, Zhiqiang Jin, Taihao Ang, Kean-Hooi Huang, Miller Haston, Kelly M Peng, Jisong Zhong, Tao P Finkbeiner, Steven Weiss, William A Arkin, Michelle R Jan, Lily Y Guo, Su Imaging-based chemical screening reveals activity-dependent neural differentiation of pluripotent stem cells |
title | Imaging-based chemical screening reveals activity-dependent neural differentiation of pluripotent stem cells |
title_full | Imaging-based chemical screening reveals activity-dependent neural differentiation of pluripotent stem cells |
title_fullStr | Imaging-based chemical screening reveals activity-dependent neural differentiation of pluripotent stem cells |
title_full_unstemmed | Imaging-based chemical screening reveals activity-dependent neural differentiation of pluripotent stem cells |
title_short | Imaging-based chemical screening reveals activity-dependent neural differentiation of pluripotent stem cells |
title_sort | imaging-based chemical screening reveals activity-dependent neural differentiation of pluripotent stem cells |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771564/ https://www.ncbi.nlm.nih.gov/pubmed/24040509 http://dx.doi.org/10.7554/eLife.00508 |
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