Cargando…
Self-organization of human dorsal-ventral forebrain structures by light induced SHH
Organizing centers secrete morphogens that specify the emergence of germ layers and the establishment of the body’s axes during embryogenesis. While traditional experimental embryology tools have been instrumental in dissecting the molecular aspects of organizers in model systems, they are impractic...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604999/ https://www.ncbi.nlm.nih.gov/pubmed/34799555 http://dx.doi.org/10.1038/s41467-021-26881-w |
_version_ | 1784602081818050560 |
---|---|
author | De Santis, Riccardo Etoc, Fred Rosado-Olivieri, Edwin A. Brivanlou, Ali H. |
author_facet | De Santis, Riccardo Etoc, Fred Rosado-Olivieri, Edwin A. Brivanlou, Ali H. |
author_sort | De Santis, Riccardo |
collection | PubMed |
description | Organizing centers secrete morphogens that specify the emergence of germ layers and the establishment of the body’s axes during embryogenesis. While traditional experimental embryology tools have been instrumental in dissecting the molecular aspects of organizers in model systems, they are impractical in human in-vitro model systems to dissect the relationships between signaling and fate along embryonic coordinates. To systematically study human embryonic organizer centers, we devised a collection of optogenetic ePiggyBac vectors to express a photoactivatable Cre-loxP recombinase, that allows the systematic induction of organizer structures by shining blue-light on human embryonic stem cells (hESCs). We used a light stimulus to geometrically confine SHH expression in neuralizing hESCs. This led to the self-organization of mediolateral neural patterns. scRNA-seq analysis established that these structures represent the dorsal-ventral forebrain, at the end of the first month of development. Here, we show that morphogen light-stimulation is a scalable tool that induces self-organizing centers. |
format | Online Article Text |
id | pubmed-8604999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86049992021-12-03 Self-organization of human dorsal-ventral forebrain structures by light induced SHH De Santis, Riccardo Etoc, Fred Rosado-Olivieri, Edwin A. Brivanlou, Ali H. Nat Commun Article Organizing centers secrete morphogens that specify the emergence of germ layers and the establishment of the body’s axes during embryogenesis. While traditional experimental embryology tools have been instrumental in dissecting the molecular aspects of organizers in model systems, they are impractical in human in-vitro model systems to dissect the relationships between signaling and fate along embryonic coordinates. To systematically study human embryonic organizer centers, we devised a collection of optogenetic ePiggyBac vectors to express a photoactivatable Cre-loxP recombinase, that allows the systematic induction of organizer structures by shining blue-light on human embryonic stem cells (hESCs). We used a light stimulus to geometrically confine SHH expression in neuralizing hESCs. This led to the self-organization of mediolateral neural patterns. scRNA-seq analysis established that these structures represent the dorsal-ventral forebrain, at the end of the first month of development. Here, we show that morphogen light-stimulation is a scalable tool that induces self-organizing centers. Nature Publishing Group UK 2021-11-19 /pmc/articles/PMC8604999/ /pubmed/34799555 http://dx.doi.org/10.1038/s41467-021-26881-w Text en © The Author(s) 2021 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 De Santis, Riccardo Etoc, Fred Rosado-Olivieri, Edwin A. Brivanlou, Ali H. Self-organization of human dorsal-ventral forebrain structures by light induced SHH |
title | Self-organization of human dorsal-ventral forebrain structures by light induced SHH |
title_full | Self-organization of human dorsal-ventral forebrain structures by light induced SHH |
title_fullStr | Self-organization of human dorsal-ventral forebrain structures by light induced SHH |
title_full_unstemmed | Self-organization of human dorsal-ventral forebrain structures by light induced SHH |
title_short | Self-organization of human dorsal-ventral forebrain structures by light induced SHH |
title_sort | self-organization of human dorsal-ventral forebrain structures by light induced shh |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604999/ https://www.ncbi.nlm.nih.gov/pubmed/34799555 http://dx.doi.org/10.1038/s41467-021-26881-w |
work_keys_str_mv | AT desantisriccardo selforganizationofhumandorsalventralforebrainstructuresbylightinducedshh AT etocfred selforganizationofhumandorsalventralforebrainstructuresbylightinducedshh AT rosadoolivieriedwina selforganizationofhumandorsalventralforebrainstructuresbylightinducedshh AT brivanloualih selforganizationofhumandorsalventralforebrainstructuresbylightinducedshh |