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Imaging neuronal migration and network activity in human forebrain assembloids

Assembloids generated from human pluripotent stem cells are self-organizing, multicellular in vitro models that recapitulate aspects of cell-cell interactions and circuit assembly during neural development. Here, we present protocols to functionally monitor, in forebrain assembloids, the migration o...

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Detalles Bibliográficos
Autores principales: Birey, Fikri, Pașca, Sergiu P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234084/
https://www.ncbi.nlm.nih.gov/pubmed/35769932
http://dx.doi.org/10.1016/j.xpro.2022.101478
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author Birey, Fikri
Pașca, Sergiu P.
author_facet Birey, Fikri
Pașca, Sergiu P.
author_sort Birey, Fikri
collection PubMed
description Assembloids generated from human pluripotent stem cells are self-organizing, multicellular in vitro models that recapitulate aspects of cell-cell interactions and circuit assembly during neural development. Here, we present protocols to functionally monitor, in forebrain assembloids, the migration of GABAergic interneurons from the ventral to the dorsal forebrain and the activity in early cortical networks. Specifically, we describe high-resolution imaging and analysis of neuronal migration as well as calcium imaging of network activity in forebrain assembloids. For complete details on the use and execution of this protocol, please refer to Birey et al. (2022).
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spelling pubmed-92340842022-06-28 Imaging neuronal migration and network activity in human forebrain assembloids Birey, Fikri Pașca, Sergiu P. STAR Protoc Protocol Assembloids generated from human pluripotent stem cells are self-organizing, multicellular in vitro models that recapitulate aspects of cell-cell interactions and circuit assembly during neural development. Here, we present protocols to functionally monitor, in forebrain assembloids, the migration of GABAergic interneurons from the ventral to the dorsal forebrain and the activity in early cortical networks. Specifically, we describe high-resolution imaging and analysis of neuronal migration as well as calcium imaging of network activity in forebrain assembloids. For complete details on the use and execution of this protocol, please refer to Birey et al. (2022). Elsevier 2022-06-17 /pmc/articles/PMC9234084/ /pubmed/35769932 http://dx.doi.org/10.1016/j.xpro.2022.101478 Text en © 2022 The Author(s) https://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 Protocol
Birey, Fikri
Pașca, Sergiu P.
Imaging neuronal migration and network activity in human forebrain assembloids
title Imaging neuronal migration and network activity in human forebrain assembloids
title_full Imaging neuronal migration and network activity in human forebrain assembloids
title_fullStr Imaging neuronal migration and network activity in human forebrain assembloids
title_full_unstemmed Imaging neuronal migration and network activity in human forebrain assembloids
title_short Imaging neuronal migration and network activity in human forebrain assembloids
title_sort imaging neuronal migration and network activity in human forebrain assembloids
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234084/
https://www.ncbi.nlm.nih.gov/pubmed/35769932
http://dx.doi.org/10.1016/j.xpro.2022.101478
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