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Activin/Nodal Signaling Supports Retinal Progenitor Specification in a Narrow Time Window during Pluripotent Stem Cell Neuralization
Retinal progenitors are initially found in the anterior neural plate region known as the eye field, whereas neighboring areas undertake telencephalic or hypothalamic development. Eye field cells become specified by switching on a network of eye field transcription factors, but the extracellular cues...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624997/ https://www.ncbi.nlm.nih.gov/pubmed/26388287 http://dx.doi.org/10.1016/j.stemcr.2015.08.011 |
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author | Bertacchi, Michele Lupo, Giuseppe Pandolfini, Luca Casarosa, Simona D’Onofrio, Mara Pedersen, Roger A. Harris, William A. Cremisi, Federico |
author_facet | Bertacchi, Michele Lupo, Giuseppe Pandolfini, Luca Casarosa, Simona D’Onofrio, Mara Pedersen, Roger A. Harris, William A. Cremisi, Federico |
author_sort | Bertacchi, Michele |
collection | PubMed |
description | Retinal progenitors are initially found in the anterior neural plate region known as the eye field, whereas neighboring areas undertake telencephalic or hypothalamic development. Eye field cells become specified by switching on a network of eye field transcription factors, but the extracellular cues activating this network remain unclear. In this study, we used chemically defined media to induce in vitro differentiation of mouse embryonic stem cells (ESCs) toward eye field fates. Inhibition of Wnt/β-catenin signaling was sufficient to drive ESCs to telencephalic, but not retinal, fates. Instead, retinal progenitors could be generated from competent differentiating mouse ESCs by activation of Activin/Nodal signaling within a narrow temporal window corresponding to the emergence of primitive anterior neural progenitors. Activin also promoted eye field gene expression in differentiating human ESCs. Our results reveal insights into the mechanisms of eye field specification and open new avenues toward the generation of retinal progenitors for translational medicine. |
format | Online Article Text |
id | pubmed-4624997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-46249972015-11-19 Activin/Nodal Signaling Supports Retinal Progenitor Specification in a Narrow Time Window during Pluripotent Stem Cell Neuralization Bertacchi, Michele Lupo, Giuseppe Pandolfini, Luca Casarosa, Simona D’Onofrio, Mara Pedersen, Roger A. Harris, William A. Cremisi, Federico Stem Cell Reports Article Retinal progenitors are initially found in the anterior neural plate region known as the eye field, whereas neighboring areas undertake telencephalic or hypothalamic development. Eye field cells become specified by switching on a network of eye field transcription factors, but the extracellular cues activating this network remain unclear. In this study, we used chemically defined media to induce in vitro differentiation of mouse embryonic stem cells (ESCs) toward eye field fates. Inhibition of Wnt/β-catenin signaling was sufficient to drive ESCs to telencephalic, but not retinal, fates. Instead, retinal progenitors could be generated from competent differentiating mouse ESCs by activation of Activin/Nodal signaling within a narrow temporal window corresponding to the emergence of primitive anterior neural progenitors. Activin also promoted eye field gene expression in differentiating human ESCs. Our results reveal insights into the mechanisms of eye field specification and open new avenues toward the generation of retinal progenitors for translational medicine. Elsevier 2015-09-17 /pmc/articles/PMC4624997/ /pubmed/26388287 http://dx.doi.org/10.1016/j.stemcr.2015.08.011 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Bertacchi, Michele Lupo, Giuseppe Pandolfini, Luca Casarosa, Simona D’Onofrio, Mara Pedersen, Roger A. Harris, William A. Cremisi, Federico Activin/Nodal Signaling Supports Retinal Progenitor Specification in a Narrow Time Window during Pluripotent Stem Cell Neuralization |
title | Activin/Nodal Signaling Supports Retinal Progenitor Specification in a Narrow Time Window during Pluripotent Stem Cell Neuralization |
title_full | Activin/Nodal Signaling Supports Retinal Progenitor Specification in a Narrow Time Window during Pluripotent Stem Cell Neuralization |
title_fullStr | Activin/Nodal Signaling Supports Retinal Progenitor Specification in a Narrow Time Window during Pluripotent Stem Cell Neuralization |
title_full_unstemmed | Activin/Nodal Signaling Supports Retinal Progenitor Specification in a Narrow Time Window during Pluripotent Stem Cell Neuralization |
title_short | Activin/Nodal Signaling Supports Retinal Progenitor Specification in a Narrow Time Window during Pluripotent Stem Cell Neuralization |
title_sort | activin/nodal signaling supports retinal progenitor specification in a narrow time window during pluripotent stem cell neuralization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624997/ https://www.ncbi.nlm.nih.gov/pubmed/26388287 http://dx.doi.org/10.1016/j.stemcr.2015.08.011 |
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