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Understanding neural development and diseases using CRISPR screens in human pluripotent stem cell-derived cultures
The brain is arguably the most complex part of the human body in form and function. Much remains unclear about the molecular mechanisms that regulate its normal and pathological physiology. This lack of knowledge largely stems from the inaccessible nature of the human brain, and the limitation of an...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123288/ https://www.ncbi.nlm.nih.gov/pubmed/37101616 http://dx.doi.org/10.3389/fcell.2023.1158373 |
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author | Ahmed, Mai Muffat, Julien Li, Yun |
author_facet | Ahmed, Mai Muffat, Julien Li, Yun |
author_sort | Ahmed, Mai |
collection | PubMed |
description | The brain is arguably the most complex part of the human body in form and function. Much remains unclear about the molecular mechanisms that regulate its normal and pathological physiology. This lack of knowledge largely stems from the inaccessible nature of the human brain, and the limitation of animal models. As a result, brain disorders are difficult to understand and even more difficult to treat. Recent advances in generating human pluripotent stem cells (hPSCs)-derived 2-dimensional (2D) and 3-dimensional (3D) neural cultures have provided an accessible system to model the human brain. Breakthroughs in gene editing technologies such as CRISPR/Cas9 further elevate the hPSCs into a genetically tractable experimental system. Powerful genetic screens, previously reserved for model organisms and transformed cell lines, can now be performed in human neural cells. Combined with the rapidly expanding single-cell genomics toolkit, these technological advances culminate to create an unprecedented opportunity to study the human brain using functional genomics. This review will summarize the current progress of applying CRISPR-based genetic screens in hPSCs-derived 2D neural cultures and 3D brain organoids. We will also evaluate the key technologies involved and discuss their related experimental considerations and future applications. |
format | Online Article Text |
id | pubmed-10123288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101232882023-04-25 Understanding neural development and diseases using CRISPR screens in human pluripotent stem cell-derived cultures Ahmed, Mai Muffat, Julien Li, Yun Front Cell Dev Biol Cell and Developmental Biology The brain is arguably the most complex part of the human body in form and function. Much remains unclear about the molecular mechanisms that regulate its normal and pathological physiology. This lack of knowledge largely stems from the inaccessible nature of the human brain, and the limitation of animal models. As a result, brain disorders are difficult to understand and even more difficult to treat. Recent advances in generating human pluripotent stem cells (hPSCs)-derived 2-dimensional (2D) and 3-dimensional (3D) neural cultures have provided an accessible system to model the human brain. Breakthroughs in gene editing technologies such as CRISPR/Cas9 further elevate the hPSCs into a genetically tractable experimental system. Powerful genetic screens, previously reserved for model organisms and transformed cell lines, can now be performed in human neural cells. Combined with the rapidly expanding single-cell genomics toolkit, these technological advances culminate to create an unprecedented opportunity to study the human brain using functional genomics. This review will summarize the current progress of applying CRISPR-based genetic screens in hPSCs-derived 2D neural cultures and 3D brain organoids. We will also evaluate the key technologies involved and discuss their related experimental considerations and future applications. Frontiers Media S.A. 2023-04-10 /pmc/articles/PMC10123288/ /pubmed/37101616 http://dx.doi.org/10.3389/fcell.2023.1158373 Text en Copyright © 2023 Ahmed, Muffat and Li. https://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 | Cell and Developmental Biology Ahmed, Mai Muffat, Julien Li, Yun Understanding neural development and diseases using CRISPR screens in human pluripotent stem cell-derived cultures |
title | Understanding neural development and diseases using CRISPR screens in human pluripotent stem cell-derived cultures |
title_full | Understanding neural development and diseases using CRISPR screens in human pluripotent stem cell-derived cultures |
title_fullStr | Understanding neural development and diseases using CRISPR screens in human pluripotent stem cell-derived cultures |
title_full_unstemmed | Understanding neural development and diseases using CRISPR screens in human pluripotent stem cell-derived cultures |
title_short | Understanding neural development and diseases using CRISPR screens in human pluripotent stem cell-derived cultures |
title_sort | understanding neural development and diseases using crispr screens in human pluripotent stem cell-derived cultures |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123288/ https://www.ncbi.nlm.nih.gov/pubmed/37101616 http://dx.doi.org/10.3389/fcell.2023.1158373 |
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