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The Rise of Retinal Organoids for Vision Research

Retinal degenerative diseases lead to irreversible blindness. Decades of research into the cellular and molecular mechanisms of retinal diseases, using either animal models or human cell-derived 2D systems, facilitated the development of several therapeutic interventions. Recently, human stem cell-d...

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Detalles Bibliográficos
Autores principales: Sharma, Kritika, Krohne, Tim U., Busskamp, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697892/
https://www.ncbi.nlm.nih.gov/pubmed/33187246
http://dx.doi.org/10.3390/ijms21228484
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author Sharma, Kritika
Krohne, Tim U.
Busskamp, Volker
author_facet Sharma, Kritika
Krohne, Tim U.
Busskamp, Volker
author_sort Sharma, Kritika
collection PubMed
description Retinal degenerative diseases lead to irreversible blindness. Decades of research into the cellular and molecular mechanisms of retinal diseases, using either animal models or human cell-derived 2D systems, facilitated the development of several therapeutic interventions. Recently, human stem cell-derived 3D retinal organoids have been developed. These self-organizing 3D organ systems have shown to recapitulate the in vivo human retinogenesis resulting in morphological and functionally similar retinal cell types in vitro. In less than a decade, retinal organoids have assisted in modeling several retinal diseases that were rather difficult to mimic in rodent models. Retinal organoids are also considered as a photoreceptor source for cell transplantation therapies to counteract blindness. Here, we highlight the development and field’s improvements of retinal organoids and discuss their application aspects as human disease models, pharmaceutical testbeds, and cell sources for transplantations.
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spelling pubmed-76978922020-11-29 The Rise of Retinal Organoids for Vision Research Sharma, Kritika Krohne, Tim U. Busskamp, Volker Int J Mol Sci Review Retinal degenerative diseases lead to irreversible blindness. Decades of research into the cellular and molecular mechanisms of retinal diseases, using either animal models or human cell-derived 2D systems, facilitated the development of several therapeutic interventions. Recently, human stem cell-derived 3D retinal organoids have been developed. These self-organizing 3D organ systems have shown to recapitulate the in vivo human retinogenesis resulting in morphological and functionally similar retinal cell types in vitro. In less than a decade, retinal organoids have assisted in modeling several retinal diseases that were rather difficult to mimic in rodent models. Retinal organoids are also considered as a photoreceptor source for cell transplantation therapies to counteract blindness. Here, we highlight the development and field’s improvements of retinal organoids and discuss their application aspects as human disease models, pharmaceutical testbeds, and cell sources for transplantations. MDPI 2020-11-11 /pmc/articles/PMC7697892/ /pubmed/33187246 http://dx.doi.org/10.3390/ijms21228484 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sharma, Kritika
Krohne, Tim U.
Busskamp, Volker
The Rise of Retinal Organoids for Vision Research
title The Rise of Retinal Organoids for Vision Research
title_full The Rise of Retinal Organoids for Vision Research
title_fullStr The Rise of Retinal Organoids for Vision Research
title_full_unstemmed The Rise of Retinal Organoids for Vision Research
title_short The Rise of Retinal Organoids for Vision Research
title_sort rise of retinal organoids for vision research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697892/
https://www.ncbi.nlm.nih.gov/pubmed/33187246
http://dx.doi.org/10.3390/ijms21228484
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