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Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish
Induction of specific neuronal fates is restricted in time and space in the developing CNS through integration of extrinsic morphogen signals and intrinsic determinants. Morphogens impose regional characteristics on neural progenitors and establish distinct progenitor domains. Such domains are defin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033221/ https://www.ncbi.nlm.nih.gov/pubmed/24904255 http://dx.doi.org/10.3389/fnins.2014.00109 |
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author | Allodi, Ilary Hedlund, Eva |
author_facet | Allodi, Ilary Hedlund, Eva |
author_sort | Allodi, Ilary |
collection | PubMed |
description | Induction of specific neuronal fates is restricted in time and space in the developing CNS through integration of extrinsic morphogen signals and intrinsic determinants. Morphogens impose regional characteristics on neural progenitors and establish distinct progenitor domains. Such domains are defined by unique expression patterns of fate determining transcription factors. These processes of neuronal fate specification can be recapitulated in vitro using pluripotent stem cells. In this review, we focus on the generation of dopamine neurons and motor neurons, which are induced at ventral positions of the neural tube through Sonic hedgehog (Shh) signaling, and defined at anteroposterior positions by fibroblast growth factor (Fgf) 8, Wnt1, and retinoic acid (RA). In vitro utilization of these morphogenic signals typically results in the generation of multiple neuronal cell types, which are defined at the intersection of these signals. If the purpose of in vitro neurogenesis is to generate one cell type only, further lineage restriction can be accomplished by forced expression of specific transcription factors in a permissive environment. Alternatively, cell-sorting strategies allow for selection of neuronal progenitors or mature neurons. However, modeling development, disease and prospective therapies in a dish could benefit from structured heterogeneity, where desired neurons are appropriately synaptically connected and thus better reflect the three-dimensional structure of that region. By modulating the extrinsic environment to direct sequential generation of neural progenitors within a domain, followed by self-organization and synaptic establishment, a reductionist model of that brain region could be created. Here we review recent advances in neuronal fate induction in vitro, with a focus on the interplay between cell intrinsic and extrinsic factors, and discuss the implications for studying development and disease in a dish. |
format | Online Article Text |
id | pubmed-4033221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40332212014-06-05 Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish Allodi, Ilary Hedlund, Eva Front Neurosci Neuroscience Induction of specific neuronal fates is restricted in time and space in the developing CNS through integration of extrinsic morphogen signals and intrinsic determinants. Morphogens impose regional characteristics on neural progenitors and establish distinct progenitor domains. Such domains are defined by unique expression patterns of fate determining transcription factors. These processes of neuronal fate specification can be recapitulated in vitro using pluripotent stem cells. In this review, we focus on the generation of dopamine neurons and motor neurons, which are induced at ventral positions of the neural tube through Sonic hedgehog (Shh) signaling, and defined at anteroposterior positions by fibroblast growth factor (Fgf) 8, Wnt1, and retinoic acid (RA). In vitro utilization of these morphogenic signals typically results in the generation of multiple neuronal cell types, which are defined at the intersection of these signals. If the purpose of in vitro neurogenesis is to generate one cell type only, further lineage restriction can be accomplished by forced expression of specific transcription factors in a permissive environment. Alternatively, cell-sorting strategies allow for selection of neuronal progenitors or mature neurons. However, modeling development, disease and prospective therapies in a dish could benefit from structured heterogeneity, where desired neurons are appropriately synaptically connected and thus better reflect the three-dimensional structure of that region. By modulating the extrinsic environment to direct sequential generation of neural progenitors within a domain, followed by self-organization and synaptic establishment, a reductionist model of that brain region could be created. Here we review recent advances in neuronal fate induction in vitro, with a focus on the interplay between cell intrinsic and extrinsic factors, and discuss the implications for studying development and disease in a dish. Frontiers Media S.A. 2014-05-20 /pmc/articles/PMC4033221/ /pubmed/24904255 http://dx.doi.org/10.3389/fnins.2014.00109 Text en Copyright © 2014 Allodi and Hedlund. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 | Neuroscience Allodi, Ilary Hedlund, Eva Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish |
title | Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish |
title_full | Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish |
title_fullStr | Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish |
title_full_unstemmed | Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish |
title_short | Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish |
title_sort | directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033221/ https://www.ncbi.nlm.nih.gov/pubmed/24904255 http://dx.doi.org/10.3389/fnins.2014.00109 |
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