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Stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis

The vertebrate eye primordium consists of a pseudostratified neuroepithelium, the optic vesicle (OV), in which cells acquire neural retina or retinal pigment epithelium (RPE) fates. As these fates arise, the OV assumes a cup shape, influenced by mechanical forces generated within the neural retina....

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Autores principales: Moreno-Mármol, Tania, Ledesma-Terrón, Mario, Tabanera, Noemi, Martin-Bermejo, Maria Jesús, Cardozo, Marcos J, Cavodeassi, Florencia, Bovolenta, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530511/
https://www.ncbi.nlm.nih.gov/pubmed/34545806
http://dx.doi.org/10.7554/eLife.63396
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author Moreno-Mármol, Tania
Ledesma-Terrón, Mario
Tabanera, Noemi
Martin-Bermejo, Maria Jesús
Cardozo, Marcos J
Cavodeassi, Florencia
Bovolenta, Paola
author_facet Moreno-Mármol, Tania
Ledesma-Terrón, Mario
Tabanera, Noemi
Martin-Bermejo, Maria Jesús
Cardozo, Marcos J
Cavodeassi, Florencia
Bovolenta, Paola
author_sort Moreno-Mármol, Tania
collection PubMed
description The vertebrate eye primordium consists of a pseudostratified neuroepithelium, the optic vesicle (OV), in which cells acquire neural retina or retinal pigment epithelium (RPE) fates. As these fates arise, the OV assumes a cup shape, influenced by mechanical forces generated within the neural retina. Whether the RPE passively adapts to retinal changes or actively contributes to OV morphogenesis remains unexplored. We generated a zebrafish Tg(E1-bhlhe40:GFP) line to track RPE morphogenesis and interrogate its participation in OV folding. We show that, in virtual absence of proliferation, RPE cells stretch and flatten, thereby matching the retinal curvature and promoting OV folding. Localized interference with the RPE cytoskeleton disrupts tissue stretching and OV folding. Thus, extreme RPE flattening and accelerated differentiation are efficient solutions adopted by fast-developing species to enable timely optic cup formation. This mechanism differs in amniotes, in which proliferation drives RPE expansion with a much-reduced need of cell flattening.
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spelling pubmed-85305112021-10-25 Stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis Moreno-Mármol, Tania Ledesma-Terrón, Mario Tabanera, Noemi Martin-Bermejo, Maria Jesús Cardozo, Marcos J Cavodeassi, Florencia Bovolenta, Paola eLife Developmental Biology The vertebrate eye primordium consists of a pseudostratified neuroepithelium, the optic vesicle (OV), in which cells acquire neural retina or retinal pigment epithelium (RPE) fates. As these fates arise, the OV assumes a cup shape, influenced by mechanical forces generated within the neural retina. Whether the RPE passively adapts to retinal changes or actively contributes to OV morphogenesis remains unexplored. We generated a zebrafish Tg(E1-bhlhe40:GFP) line to track RPE morphogenesis and interrogate its participation in OV folding. We show that, in virtual absence of proliferation, RPE cells stretch and flatten, thereby matching the retinal curvature and promoting OV folding. Localized interference with the RPE cytoskeleton disrupts tissue stretching and OV folding. Thus, extreme RPE flattening and accelerated differentiation are efficient solutions adopted by fast-developing species to enable timely optic cup formation. This mechanism differs in amniotes, in which proliferation drives RPE expansion with a much-reduced need of cell flattening. eLife Sciences Publications, Ltd 2021-09-21 /pmc/articles/PMC8530511/ /pubmed/34545806 http://dx.doi.org/10.7554/eLife.63396 Text en © 2021, Moreno-Mármol et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Moreno-Mármol, Tania
Ledesma-Terrón, Mario
Tabanera, Noemi
Martin-Bermejo, Maria Jesús
Cardozo, Marcos J
Cavodeassi, Florencia
Bovolenta, Paola
Stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis
title Stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis
title_full Stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis
title_fullStr Stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis
title_full_unstemmed Stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis
title_short Stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis
title_sort stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530511/
https://www.ncbi.nlm.nih.gov/pubmed/34545806
http://dx.doi.org/10.7554/eLife.63396
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