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Using human pluripotent stem cell models to study autism in the era of big data
Advances in human pluripotent stem cell (hPSC) biology coupled with protocols to generate diverse brain cell types in vitro have provided neuroscientists with opportunities to dissect basic and disease mechanisms in increasingly relevant cellular substrates. At the same time, large data collections...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087382/ https://www.ncbi.nlm.nih.gov/pubmed/32293529 http://dx.doi.org/10.1186/s13229-020-00322-9 |
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author | Nehme, Ralda Barrett, Lindy E. |
author_facet | Nehme, Ralda Barrett, Lindy E. |
author_sort | Nehme, Ralda |
collection | PubMed |
description | Advances in human pluripotent stem cell (hPSC) biology coupled with protocols to generate diverse brain cell types in vitro have provided neuroscientists with opportunities to dissect basic and disease mechanisms in increasingly relevant cellular substrates. At the same time, large data collections and analyses have facilitated unprecedented insights into autism genetics, normal human genetic variation, and the molecular landscape of the developing human brain. While such insights have enabled the investigation of key mechanistic questions in autism, they also highlight important limitations associated with the use of existing hPSC models. In this review, we discuss four such issues which influence the efficacy of hPSC models for studying autism, including (i) sources of variance, (ii) scale and format of study design, (iii) divergence from the human brain in vivo, and (iv) regulatory policies and compliance governing the use of hPSCs. Moreover, we advocate for a set of immediate and long-term priorities to address these issues and to accelerate the generation and reproducibility of data in order to facilitate future fundamental as well as therapeutic discoveries. |
format | Online Article Text |
id | pubmed-7087382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70873822020-03-24 Using human pluripotent stem cell models to study autism in the era of big data Nehme, Ralda Barrett, Lindy E. Mol Autism Review Advances in human pluripotent stem cell (hPSC) biology coupled with protocols to generate diverse brain cell types in vitro have provided neuroscientists with opportunities to dissect basic and disease mechanisms in increasingly relevant cellular substrates. At the same time, large data collections and analyses have facilitated unprecedented insights into autism genetics, normal human genetic variation, and the molecular landscape of the developing human brain. While such insights have enabled the investigation of key mechanistic questions in autism, they also highlight important limitations associated with the use of existing hPSC models. In this review, we discuss four such issues which influence the efficacy of hPSC models for studying autism, including (i) sources of variance, (ii) scale and format of study design, (iii) divergence from the human brain in vivo, and (iv) regulatory policies and compliance governing the use of hPSCs. Moreover, we advocate for a set of immediate and long-term priorities to address these issues and to accelerate the generation and reproducibility of data in order to facilitate future fundamental as well as therapeutic discoveries. BioMed Central 2020-03-23 /pmc/articles/PMC7087382/ /pubmed/32293529 http://dx.doi.org/10.1186/s13229-020-00322-9 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Nehme, Ralda Barrett, Lindy E. Using human pluripotent stem cell models to study autism in the era of big data |
title | Using human pluripotent stem cell models to study autism in the era of big data |
title_full | Using human pluripotent stem cell models to study autism in the era of big data |
title_fullStr | Using human pluripotent stem cell models to study autism in the era of big data |
title_full_unstemmed | Using human pluripotent stem cell models to study autism in the era of big data |
title_short | Using human pluripotent stem cell models to study autism in the era of big data |
title_sort | using human pluripotent stem cell models to study autism in the era of big data |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087382/ https://www.ncbi.nlm.nih.gov/pubmed/32293529 http://dx.doi.org/10.1186/s13229-020-00322-9 |
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