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Spatiotemporal, optogenetic control of gene expression in organoids

Organoids derived from stem cells have become an increasingly important tool for studying human development and modeling disease. However, methods are still needed to control and study spatiotemporal patterns of gene expression in organoids. Here we combined optogenetics and gene perturbation techno...

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Autores principales: Legnini, Ivano, Emmenegger, Lisa, Zappulo, Alessandra, Rybak-Wolf, Agnieszka, Wurmus, Ricardo, Martinez, Anna Oliveras, Jara, Cledi Cerda, Boltengagen, Anastasiya, Hessler, Talé, Mastrobuoni, Guido, Kempa, Stefan, Zinzen, Robert, Woehler, Andrew, Rajewsky, Nikolaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555836/
https://www.ncbi.nlm.nih.gov/pubmed/37735569
http://dx.doi.org/10.1038/s41592-023-01986-w
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author Legnini, Ivano
Emmenegger, Lisa
Zappulo, Alessandra
Rybak-Wolf, Agnieszka
Wurmus, Ricardo
Martinez, Anna Oliveras
Jara, Cledi Cerda
Boltengagen, Anastasiya
Hessler, Talé
Mastrobuoni, Guido
Kempa, Stefan
Zinzen, Robert
Woehler, Andrew
Rajewsky, Nikolaus
author_facet Legnini, Ivano
Emmenegger, Lisa
Zappulo, Alessandra
Rybak-Wolf, Agnieszka
Wurmus, Ricardo
Martinez, Anna Oliveras
Jara, Cledi Cerda
Boltengagen, Anastasiya
Hessler, Talé
Mastrobuoni, Guido
Kempa, Stefan
Zinzen, Robert
Woehler, Andrew
Rajewsky, Nikolaus
author_sort Legnini, Ivano
collection PubMed
description Organoids derived from stem cells have become an increasingly important tool for studying human development and modeling disease. However, methods are still needed to control and study spatiotemporal patterns of gene expression in organoids. Here we combined optogenetics and gene perturbation technologies to activate or knock-down RNA of target genes in programmable spatiotemporal patterns. To illustrate the usefulness of our approach, we locally activated Sonic Hedgehog (SHH) signaling in an organoid model for human neurodevelopment. Spatial and single-cell transcriptomic analyses showed that this local induction was sufficient to generate stereotypically patterned organoids and revealed new insights into SHH’s contribution to gene regulation in neurodevelopment. With this study, we propose optogenetic perturbations in combination with spatial transcriptomics as a powerful technology to reprogram and study cell fates and tissue patterning in organoids.
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spelling pubmed-105558362023-10-07 Spatiotemporal, optogenetic control of gene expression in organoids Legnini, Ivano Emmenegger, Lisa Zappulo, Alessandra Rybak-Wolf, Agnieszka Wurmus, Ricardo Martinez, Anna Oliveras Jara, Cledi Cerda Boltengagen, Anastasiya Hessler, Talé Mastrobuoni, Guido Kempa, Stefan Zinzen, Robert Woehler, Andrew Rajewsky, Nikolaus Nat Methods Article Organoids derived from stem cells have become an increasingly important tool for studying human development and modeling disease. However, methods are still needed to control and study spatiotemporal patterns of gene expression in organoids. Here we combined optogenetics and gene perturbation technologies to activate or knock-down RNA of target genes in programmable spatiotemporal patterns. To illustrate the usefulness of our approach, we locally activated Sonic Hedgehog (SHH) signaling in an organoid model for human neurodevelopment. Spatial and single-cell transcriptomic analyses showed that this local induction was sufficient to generate stereotypically patterned organoids and revealed new insights into SHH’s contribution to gene regulation in neurodevelopment. With this study, we propose optogenetic perturbations in combination with spatial transcriptomics as a powerful technology to reprogram and study cell fates and tissue patterning in organoids. Nature Publishing Group US 2023-09-21 2023 /pmc/articles/PMC10555836/ /pubmed/37735569 http://dx.doi.org/10.1038/s41592-023-01986-w 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
Legnini, Ivano
Emmenegger, Lisa
Zappulo, Alessandra
Rybak-Wolf, Agnieszka
Wurmus, Ricardo
Martinez, Anna Oliveras
Jara, Cledi Cerda
Boltengagen, Anastasiya
Hessler, Talé
Mastrobuoni, Guido
Kempa, Stefan
Zinzen, Robert
Woehler, Andrew
Rajewsky, Nikolaus
Spatiotemporal, optogenetic control of gene expression in organoids
title Spatiotemporal, optogenetic control of gene expression in organoids
title_full Spatiotemporal, optogenetic control of gene expression in organoids
title_fullStr Spatiotemporal, optogenetic control of gene expression in organoids
title_full_unstemmed Spatiotemporal, optogenetic control of gene expression in organoids
title_short Spatiotemporal, optogenetic control of gene expression in organoids
title_sort spatiotemporal, optogenetic control of gene expression in organoids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555836/
https://www.ncbi.nlm.nih.gov/pubmed/37735569
http://dx.doi.org/10.1038/s41592-023-01986-w
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