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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...

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Autores principales: Nehme, Ralda, Barrett, Lindy E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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.
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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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