Murine cerebral organoids develop network of functional neurons and hippocampal brain region identity

Summary: Brain organoids are in vitro three-dimensional (3D) self-organized neural structures, which can enable disease modeling and drug screening. However, their use for standardized large-scale drug screening studies is limited by their high batch-to-batch variability, long differentiation time (...

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Autores principales: Francesca Ciarpella, Raluca Georgiana Zamfir, Alessandra Campanelli, Elisa Ren, Giulia Pedrotti, Emanuela Bottani, Andrea Borioli, Davide Caron, Marzia Di Chio, Sissi Dolci, Annika Ahtiainen, Giorgio Malpeli, Giovanni Malerba, Rita Bardoni, Guido Fumagalli, Jari Hyttinen, Francesco Bifari, Gemma Palazzolo, Gabriella Panuccio, Giulia Curia, Ilaria Decimo
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Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/d26282c5638e451288e865f40866d9b8
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spelling oai:doaj.org-article:d26282c5638e451288e865f40866d9b82021-12-02T05:03:30ZMurine cerebral organoids develop network of functional neurons and hippocampal brain region identity2589-004210.1016/j.isci.2021.103438https://doaj.org/article/d26282c5638e451288e865f40866d9b82021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2589004221014097https://doaj.org/toc/2589-0042Summary: Brain organoids are in vitro three-dimensional (3D) self-organized neural structures, which can enable disease modeling and drug screening. However, their use for standardized large-scale drug screening studies is limited by their high batch-to-batch variability, long differentiation time (10–20 weeks), and high production costs. This is particularly relevant when brain organoids are obtained from human induced pluripotent stem cells (iPSCs). Here, we developed, for the first time, a highly standardized, reproducible, and fast (5 weeks) murine brain organoid model starting from embryonic neural stem cells. We obtained brain organoids, which progressively differentiated and self-organized into 3D networks of functional neurons with dorsal forebrain phenotype. Furthermore, by adding the morphogen WNT3a, we generated brain organoids with specific hippocampal region identity. Overall, our results showed the establishment of a fast, robust and reproducible murine 3D in vitro brain model that may represent a useful tool for high-throughput drug screening and disease modeling.Francesca CiarpellaRaluca Georgiana ZamfirAlessandra CampanelliElisa RenGiulia PedrottiEmanuela BottaniAndrea BorioliDavide CaronMarzia Di ChioSissi DolciAnnika AhtiainenGiorgio MalpeliGiovanni MalerbaRita BardoniGuido FumagalliJari HyttinenFrancesco BifariGemma PalazzoloGabriella PanuccioGiulia CuriaIlaria DecimoElsevierarticleBiological sciencesNeuroscienceCell biologyDevelopmental biologyScienceQENiScience, Vol 24, Iss 12, Pp 103438- (2021)
institution DOAJ
collection DOAJ
language EN
topic Biological sciences
Neuroscience
Cell biology
Developmental biology
Science
Q
spellingShingle Biological sciences
Neuroscience
Cell biology
Developmental biology
Science
Q
Francesca Ciarpella
Raluca Georgiana Zamfir
Alessandra Campanelli
Elisa Ren
Giulia Pedrotti
Emanuela Bottani
Andrea Borioli
Davide Caron
Marzia Di Chio
Sissi Dolci
Annika Ahtiainen
Giorgio Malpeli
Giovanni Malerba
Rita Bardoni
Guido Fumagalli
Jari Hyttinen
Francesco Bifari
Gemma Palazzolo
Gabriella Panuccio
Giulia Curia
Ilaria Decimo
Murine cerebral organoids develop network of functional neurons and hippocampal brain region identity
description Summary: Brain organoids are in vitro three-dimensional (3D) self-organized neural structures, which can enable disease modeling and drug screening. However, their use for standardized large-scale drug screening studies is limited by their high batch-to-batch variability, long differentiation time (10–20 weeks), and high production costs. This is particularly relevant when brain organoids are obtained from human induced pluripotent stem cells (iPSCs). Here, we developed, for the first time, a highly standardized, reproducible, and fast (5 weeks) murine brain organoid model starting from embryonic neural stem cells. We obtained brain organoids, which progressively differentiated and self-organized into 3D networks of functional neurons with dorsal forebrain phenotype. Furthermore, by adding the morphogen WNT3a, we generated brain organoids with specific hippocampal region identity. Overall, our results showed the establishment of a fast, robust and reproducible murine 3D in vitro brain model that may represent a useful tool for high-throughput drug screening and disease modeling.
format article
author Francesca Ciarpella
Raluca Georgiana Zamfir
Alessandra Campanelli
Elisa Ren
Giulia Pedrotti
Emanuela Bottani
Andrea Borioli
Davide Caron
Marzia Di Chio
Sissi Dolci
Annika Ahtiainen
Giorgio Malpeli
Giovanni Malerba
Rita Bardoni
Guido Fumagalli
Jari Hyttinen
Francesco Bifari
Gemma Palazzolo
Gabriella Panuccio
Giulia Curia
Ilaria Decimo
author_facet Francesca Ciarpella
Raluca Georgiana Zamfir
Alessandra Campanelli
Elisa Ren
Giulia Pedrotti
Emanuela Bottani
Andrea Borioli
Davide Caron
Marzia Di Chio
Sissi Dolci
Annika Ahtiainen
Giorgio Malpeli
Giovanni Malerba
Rita Bardoni
Guido Fumagalli
Jari Hyttinen
Francesco Bifari
Gemma Palazzolo
Gabriella Panuccio
Giulia Curia
Ilaria Decimo
author_sort Francesca Ciarpella
title Murine cerebral organoids develop network of functional neurons and hippocampal brain region identity
title_short Murine cerebral organoids develop network of functional neurons and hippocampal brain region identity
title_full Murine cerebral organoids develop network of functional neurons and hippocampal brain region identity
title_fullStr Murine cerebral organoids develop network of functional neurons and hippocampal brain region identity
title_full_unstemmed Murine cerebral organoids develop network of functional neurons and hippocampal brain region identity
title_sort murine cerebral organoids develop network of functional neurons and hippocampal brain region identity
publisher Elsevier
publishDate 2021
url https://doaj.org/article/d26282c5638e451288e865f40866d9b8
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