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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
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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. |
format | Online Article Text |
id | pubmed-10555836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
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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