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Organoids for the Study of Retinal Development and Developmental Abnormalities

The cumulative knowledge of retina development has been instrumental in the generation of retinal organoid systems from pluripotent stem cells; and these three-dimensional organoid models, in turn, have provided unprecedented opportunities for retinal research and translational applications, includi...

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Autores principales: Vielle, Anne, Park, Yuna K., Secora, Conner, Vergara, M. Natalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131530/
https://www.ncbi.nlm.nih.gov/pubmed/34025363
http://dx.doi.org/10.3389/fncel.2021.667880
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author Vielle, Anne
Park, Yuna K.
Secora, Conner
Vergara, M. Natalia
author_facet Vielle, Anne
Park, Yuna K.
Secora, Conner
Vergara, M. Natalia
author_sort Vielle, Anne
collection PubMed
description The cumulative knowledge of retina development has been instrumental in the generation of retinal organoid systems from pluripotent stem cells; and these three-dimensional organoid models, in turn, have provided unprecedented opportunities for retinal research and translational applications, including the ability to model disease in a human setting and to apply these models to the development and validation of therapeutic drugs. In this review article, we examine how retinal organoids can also contribute to our understanding of retinal developmental mechanisms, how this knowledge can be applied to modeling developmental abnormalities, and highlight some of the avenues that remain to be explored.
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spelling pubmed-81315302021-05-20 Organoids for the Study of Retinal Development and Developmental Abnormalities Vielle, Anne Park, Yuna K. Secora, Conner Vergara, M. Natalia Front Cell Neurosci Cellular Neuroscience The cumulative knowledge of retina development has been instrumental in the generation of retinal organoid systems from pluripotent stem cells; and these three-dimensional organoid models, in turn, have provided unprecedented opportunities for retinal research and translational applications, including the ability to model disease in a human setting and to apply these models to the development and validation of therapeutic drugs. In this review article, we examine how retinal organoids can also contribute to our understanding of retinal developmental mechanisms, how this knowledge can be applied to modeling developmental abnormalities, and highlight some of the avenues that remain to be explored. Frontiers Media S.A. 2021-05-05 /pmc/articles/PMC8131530/ /pubmed/34025363 http://dx.doi.org/10.3389/fncel.2021.667880 Text en Copyright © 2021 Vielle, Park, Secora and Vergara. 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 Cellular Neuroscience
Vielle, Anne
Park, Yuna K.
Secora, Conner
Vergara, M. Natalia
Organoids for the Study of Retinal Development and Developmental Abnormalities
title Organoids for the Study of Retinal Development and Developmental Abnormalities
title_full Organoids for the Study of Retinal Development and Developmental Abnormalities
title_fullStr Organoids for the Study of Retinal Development and Developmental Abnormalities
title_full_unstemmed Organoids for the Study of Retinal Development and Developmental Abnormalities
title_short Organoids for the Study of Retinal Development and Developmental Abnormalities
title_sort organoids for the study of retinal development and developmental abnormalities
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131530/
https://www.ncbi.nlm.nih.gov/pubmed/34025363
http://dx.doi.org/10.3389/fncel.2021.667880
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