Yap Regulates Müller Glia Reprogramming in Damaged Zebrafish Retinas

Vertebrates such as zebrafish have the outstanding ability to fully regenerate their retina upon injury, while mammals, including humans, do not. In zebrafish, upon light-induced injury, photoreceptor regeneration is achieved through reprogramming of Müller glia cells, which proliferate and give ris...

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Main Authors: Raquel Lourenço, Ana S. Brandão, Jorge Borbinha, Rita Gorgulho, António Jacinto
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2021.667796/full
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spelling doaj-dfa295dc71e241cd96ce6fa1f691a0a02021-09-20T05:02:13ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-09-01910.3389/fcell.2021.667796667796Yap Regulates Müller Glia Reprogramming in Damaged Zebrafish RetinasRaquel LourençoAna S. BrandãoJorge BorbinhaRita GorgulhoAntónio JacintoVertebrates such as zebrafish have the outstanding ability to fully regenerate their retina upon injury, while mammals, including humans, do not. In zebrafish, upon light-induced injury, photoreceptor regeneration is achieved through reprogramming of Müller glia cells, which proliferate and give rise to a self-renewing population of progenitors that migrate to the lesion site to differentiate into the new photoreceptors. The Hippo pathway effector YAP was recently implicated in the response to damage in the retina, but how this transcription coactivator is integrated into the signaling network regulating Müller glia reprogramming has not yet been explored. Here, we show that Yap is required in Müller glia to engage their response to a lesion by regulating their cell cycle reentry and progenitor cell formation, contributing to the differentiation of new photoreceptors. We propose that this regulation is accomplished through a lin28a–ascl1a-dependent mechanism, bona fide Müller glia-reprogramming factors. Overall, this study presents Yap as a key regulator of zebrafish Müller glia reprogramming and consequently retina regeneration upon injury.https://www.frontiersin.org/articles/10.3389/fcell.2021.667796/fullzebrafishretinaregenerationHippo-yapMüller glia
collection DOAJ
language English
format Article
sources DOAJ
author Raquel Lourenço
Ana S. Brandão
Jorge Borbinha
Rita Gorgulho
António Jacinto
spellingShingle Raquel Lourenço
Ana S. Brandão
Jorge Borbinha
Rita Gorgulho
António Jacinto
Yap Regulates Müller Glia Reprogramming in Damaged Zebrafish Retinas
Frontiers in Cell and Developmental Biology
zebrafish
retina
regeneration
Hippo-yap
Müller glia
author_facet Raquel Lourenço
Ana S. Brandão
Jorge Borbinha
Rita Gorgulho
António Jacinto
author_sort Raquel Lourenço
title Yap Regulates Müller Glia Reprogramming in Damaged Zebrafish Retinas
title_short Yap Regulates Müller Glia Reprogramming in Damaged Zebrafish Retinas
title_full Yap Regulates Müller Glia Reprogramming in Damaged Zebrafish Retinas
title_fullStr Yap Regulates Müller Glia Reprogramming in Damaged Zebrafish Retinas
title_full_unstemmed Yap Regulates Müller Glia Reprogramming in Damaged Zebrafish Retinas
title_sort yap regulates müller glia reprogramming in damaged zebrafish retinas
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2021-09-01
description Vertebrates such as zebrafish have the outstanding ability to fully regenerate their retina upon injury, while mammals, including humans, do not. In zebrafish, upon light-induced injury, photoreceptor regeneration is achieved through reprogramming of Müller glia cells, which proliferate and give rise to a self-renewing population of progenitors that migrate to the lesion site to differentiate into the new photoreceptors. The Hippo pathway effector YAP was recently implicated in the response to damage in the retina, but how this transcription coactivator is integrated into the signaling network regulating Müller glia reprogramming has not yet been explored. Here, we show that Yap is required in Müller glia to engage their response to a lesion by regulating their cell cycle reentry and progenitor cell formation, contributing to the differentiation of new photoreceptors. We propose that this regulation is accomplished through a lin28a–ascl1a-dependent mechanism, bona fide Müller glia-reprogramming factors. Overall, this study presents Yap as a key regulator of zebrafish Müller glia reprogramming and consequently retina regeneration upon injury.
topic zebrafish
retina
regeneration
Hippo-yap
Müller glia
url https://www.frontiersin.org/articles/10.3389/fcell.2021.667796/full
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