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Genetic Modification of Brain Organoids

Brain organoids have become increasingly used systems allowing 3D-modeling of human brain development, evolution, and disease. To be able to make full use of these modeling systems, researchers have developed a growing toolkit of genetic modification techniques. These techniques can be applied to ma...

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Detalles Bibliográficos
Autores principales: Fischer, Jan, Heide, Michael, Huttner, Wieland B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928125/
https://www.ncbi.nlm.nih.gov/pubmed/31920558
http://dx.doi.org/10.3389/fncel.2019.00558
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author Fischer, Jan
Heide, Michael
Huttner, Wieland B.
author_facet Fischer, Jan
Heide, Michael
Huttner, Wieland B.
author_sort Fischer, Jan
collection PubMed
description Brain organoids have become increasingly used systems allowing 3D-modeling of human brain development, evolution, and disease. To be able to make full use of these modeling systems, researchers have developed a growing toolkit of genetic modification techniques. These techniques can be applied to mature brain organoids or to the preceding embryoid bodies (EBs) and founding cells. This review will describe techniques used for transient and stable genetic modification of brain organoids and discuss their current use and respective advantages and disadvantages. Transient approaches include adeno-associated virus (AAV) and electroporation-based techniques, whereas stable genetic modification approaches make use of lentivirus (including viral stamping), transposon and CRISPR/Cas9 systems. Finally, an outlook as to likely future developments and applications regarding genetic modifications of brain organoids will be presented.
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spelling pubmed-69281252020-01-09 Genetic Modification of Brain Organoids Fischer, Jan Heide, Michael Huttner, Wieland B. Front Cell Neurosci Cellular Neuroscience Brain organoids have become increasingly used systems allowing 3D-modeling of human brain development, evolution, and disease. To be able to make full use of these modeling systems, researchers have developed a growing toolkit of genetic modification techniques. These techniques can be applied to mature brain organoids or to the preceding embryoid bodies (EBs) and founding cells. This review will describe techniques used for transient and stable genetic modification of brain organoids and discuss their current use and respective advantages and disadvantages. Transient approaches include adeno-associated virus (AAV) and electroporation-based techniques, whereas stable genetic modification approaches make use of lentivirus (including viral stamping), transposon and CRISPR/Cas9 systems. Finally, an outlook as to likely future developments and applications regarding genetic modifications of brain organoids will be presented. Frontiers Media S.A. 2019-12-17 /pmc/articles/PMC6928125/ /pubmed/31920558 http://dx.doi.org/10.3389/fncel.2019.00558 Text en Copyright © 2019 Fischer, Heide and Huttner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular Neuroscience
Fischer, Jan
Heide, Michael
Huttner, Wieland B.
Genetic Modification of Brain Organoids
title Genetic Modification of Brain Organoids
title_full Genetic Modification of Brain Organoids
title_fullStr Genetic Modification of Brain Organoids
title_full_unstemmed Genetic Modification of Brain Organoids
title_short Genetic Modification of Brain Organoids
title_sort genetic modification of brain organoids
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928125/
https://www.ncbi.nlm.nih.gov/pubmed/31920558
http://dx.doi.org/10.3389/fncel.2019.00558
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