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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....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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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. |
format | Online Article Text |
id | pubmed-8530511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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