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Role of SHH in Patterning Human Pluripotent Cells towards Ventral Forebrain Fates
The complexities of human neurodevelopment have historically been challenging to decipher but continue to be of great interest in the contexts of healthy neurobiology and disease. The classic animal models and monolayer in vitro systems have limited the types of questions scientists can strive to an...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073580/ https://www.ncbi.nlm.nih.gov/pubmed/33923415 http://dx.doi.org/10.3390/cells10040914 |
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author | Brady, Melanie V. Vaccarino, Flora M. |
author_facet | Brady, Melanie V. Vaccarino, Flora M. |
author_sort | Brady, Melanie V. |
collection | PubMed |
description | The complexities of human neurodevelopment have historically been challenging to decipher but continue to be of great interest in the contexts of healthy neurobiology and disease. The classic animal models and monolayer in vitro systems have limited the types of questions scientists can strive to answer in addition to the technical ability to answer them. However, the tridimensional human stem cell-derived organoid system provides the unique opportunity to model human development and mimic the diverse cellular composition of human organs. This strategy is adaptable and malleable, and these neural organoids possess the morphogenic sensitivity to be patterned in various ways to generate the different regions of the human brain. Furthermore, recapitulating human development provides a platform for disease modeling. One master regulator of human neurodevelopment in many regions of the human brain is sonic hedgehog (SHH), whose expression gradient and pathway activation are responsible for conferring ventral identity and shaping cellular phenotypes throughout the neural axis. This review first discusses the benefits, challenges, and limitations of using organoids for studying human neurodevelopment and disease, comparing advantages and disadvantages with other in vivo and in vitro model systems. Next, we explore the range of control that SHH exhibits on human neurodevelopment, and the application of SHH to various stem cell methodologies, including organoids, to expand our understanding of human development and disease. We outline how this strategy will eventually bring us much closer to uncovering the intricacies of human neurodevelopment and biology. |
format | Online Article Text |
id | pubmed-8073580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80735802021-04-27 Role of SHH in Patterning Human Pluripotent Cells towards Ventral Forebrain Fates Brady, Melanie V. Vaccarino, Flora M. Cells Review The complexities of human neurodevelopment have historically been challenging to decipher but continue to be of great interest in the contexts of healthy neurobiology and disease. The classic animal models and monolayer in vitro systems have limited the types of questions scientists can strive to answer in addition to the technical ability to answer them. However, the tridimensional human stem cell-derived organoid system provides the unique opportunity to model human development and mimic the diverse cellular composition of human organs. This strategy is adaptable and malleable, and these neural organoids possess the morphogenic sensitivity to be patterned in various ways to generate the different regions of the human brain. Furthermore, recapitulating human development provides a platform for disease modeling. One master regulator of human neurodevelopment in many regions of the human brain is sonic hedgehog (SHH), whose expression gradient and pathway activation are responsible for conferring ventral identity and shaping cellular phenotypes throughout the neural axis. This review first discusses the benefits, challenges, and limitations of using organoids for studying human neurodevelopment and disease, comparing advantages and disadvantages with other in vivo and in vitro model systems. Next, we explore the range of control that SHH exhibits on human neurodevelopment, and the application of SHH to various stem cell methodologies, including organoids, to expand our understanding of human development and disease. We outline how this strategy will eventually bring us much closer to uncovering the intricacies of human neurodevelopment and biology. MDPI 2021-04-16 /pmc/articles/PMC8073580/ /pubmed/33923415 http://dx.doi.org/10.3390/cells10040914 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Brady, Melanie V. Vaccarino, Flora M. Role of SHH in Patterning Human Pluripotent Cells towards Ventral Forebrain Fates |
title | Role of SHH in Patterning Human Pluripotent Cells towards Ventral Forebrain Fates |
title_full | Role of SHH in Patterning Human Pluripotent Cells towards Ventral Forebrain Fates |
title_fullStr | Role of SHH in Patterning Human Pluripotent Cells towards Ventral Forebrain Fates |
title_full_unstemmed | Role of SHH in Patterning Human Pluripotent Cells towards Ventral Forebrain Fates |
title_short | Role of SHH in Patterning Human Pluripotent Cells towards Ventral Forebrain Fates |
title_sort | role of shh in patterning human pluripotent cells towards ventral forebrain fates |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073580/ https://www.ncbi.nlm.nih.gov/pubmed/33923415 http://dx.doi.org/10.3390/cells10040914 |
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