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Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells

Retinal progenitor cells (RPCs) are the source of all retinal cell types during retinogenesis. Until now, the isolation and expansion of RPCs has been at the expense of their multipotency. Here, we report simple methods and media for the generation, expansion, and cryopreservation of human induced p...

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Autores principales: Gozlan, Sandy, Batoumeni, Vivien, Fournier, Tara, Nanteau, Céline, Potey, Anais, Clémençon, Marilou, Orieux, Gaël, Sahel, José-Alain, Goureau, Olivier, Roger, Jérôme E., Reichman, Sacha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362027/
https://www.ncbi.nlm.nih.gov/pubmed/37479765
http://dx.doi.org/10.1038/s42003-023-04956-2
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author Gozlan, Sandy
Batoumeni, Vivien
Fournier, Tara
Nanteau, Céline
Potey, Anais
Clémençon, Marilou
Orieux, Gaël
Sahel, José-Alain
Goureau, Olivier
Roger, Jérôme E.
Reichman, Sacha
author_facet Gozlan, Sandy
Batoumeni, Vivien
Fournier, Tara
Nanteau, Céline
Potey, Anais
Clémençon, Marilou
Orieux, Gaël
Sahel, José-Alain
Goureau, Olivier
Roger, Jérôme E.
Reichman, Sacha
author_sort Gozlan, Sandy
collection PubMed
description Retinal progenitor cells (RPCs) are the source of all retinal cell types during retinogenesis. Until now, the isolation and expansion of RPCs has been at the expense of their multipotency. Here, we report simple methods and media for the generation, expansion, and cryopreservation of human induced pluripotent stem-cell derived-RPCs (hiRPCs). Thawed and passed hiRPCs maintained biochemical and transcriptional RPC phenotypes and their ability to differentiate into all retinal cell types. Specific conditions allowed the generation of large cultures of photoreceptor precursors enriched up to 90% within a few weeks and without a purification step. Combined RNA-seq analysis between hiRPCs and retinal organoids identified genes involved in developmental or degenerative retinal diseases. Thus, hiRPC lines could provide a valuable source of retinal cells for cell-based therapies or drug discovery and could be an advanced cellular tool to better understand retinal dystrophies.
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spelling pubmed-103620272023-07-23 Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells Gozlan, Sandy Batoumeni, Vivien Fournier, Tara Nanteau, Céline Potey, Anais Clémençon, Marilou Orieux, Gaël Sahel, José-Alain Goureau, Olivier Roger, Jérôme E. Reichman, Sacha Commun Biol Article Retinal progenitor cells (RPCs) are the source of all retinal cell types during retinogenesis. Until now, the isolation and expansion of RPCs has been at the expense of their multipotency. Here, we report simple methods and media for the generation, expansion, and cryopreservation of human induced pluripotent stem-cell derived-RPCs (hiRPCs). Thawed and passed hiRPCs maintained biochemical and transcriptional RPC phenotypes and their ability to differentiate into all retinal cell types. Specific conditions allowed the generation of large cultures of photoreceptor precursors enriched up to 90% within a few weeks and without a purification step. Combined RNA-seq analysis between hiRPCs and retinal organoids identified genes involved in developmental or degenerative retinal diseases. Thus, hiRPC lines could provide a valuable source of retinal cells for cell-based therapies or drug discovery and could be an advanced cellular tool to better understand retinal dystrophies. Nature Publishing Group UK 2023-07-21 /pmc/articles/PMC10362027/ /pubmed/37479765 http://dx.doi.org/10.1038/s42003-023-04956-2 Text en © The Author(s) 2023 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gozlan, Sandy
Batoumeni, Vivien
Fournier, Tara
Nanteau, Céline
Potey, Anais
Clémençon, Marilou
Orieux, Gaël
Sahel, José-Alain
Goureau, Olivier
Roger, Jérôme E.
Reichman, Sacha
Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells
title Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells
title_full Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells
title_fullStr Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells
title_full_unstemmed Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells
title_short Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells
title_sort bankable human ipsc-derived retinal progenitors represent a valuable source of multipotent cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362027/
https://www.ncbi.nlm.nih.gov/pubmed/37479765
http://dx.doi.org/10.1038/s42003-023-04956-2
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