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De novo neurogenesis by targeted expression of atoh7 to Müller glia cells

Regenerative responses in the vertebrate CNS depend on quiescent radial glia stem cells, which re-enter the cell cycle and eventually differentiate into neurons. The entry into the cell cycle and the differentiation into neurons are events of opposite nature, and therefore efforts to force quiescent...

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Autores principales: Lust, Katharina, Sinn, Rebecca, Pérez Saturnino, Alicia, Centanin, Lázaro, Wittbrodt, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920165/
https://www.ncbi.nlm.nih.gov/pubmed/27068106
http://dx.doi.org/10.1242/dev.135905
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author Lust, Katharina
Sinn, Rebecca
Pérez Saturnino, Alicia
Centanin, Lázaro
Wittbrodt, Joachim
author_facet Lust, Katharina
Sinn, Rebecca
Pérez Saturnino, Alicia
Centanin, Lázaro
Wittbrodt, Joachim
author_sort Lust, Katharina
collection PubMed
description Regenerative responses in the vertebrate CNS depend on quiescent radial glia stem cells, which re-enter the cell cycle and eventually differentiate into neurons. The entry into the cell cycle and the differentiation into neurons are events of opposite nature, and therefore efforts to force quiescent radial glia into neurons require different factors. Here, we use fish to show that a single neurogenic factor, Atoh7, directs retinal radial glia (Müller glia, MG) into proliferation. The resulting neurogenic clusters differentiate in vivo into various retinal neurons. We use signaling reporters to demonstrate that the Atoh7-induced regeneration-like response of MG cells is mimicked by Notch, resembling the behavior of early progenitors during retinogenesis. Activation of Notch signaling in MG cells is sufficient to trigger proliferation and differentiation. Our results uncover a new role for Atoh7 as a universal neurogenic factor, and illustrate how signaling modules are re-employed in diverse contexts to trigger different biological responses.
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spelling pubmed-49201652016-07-25 De novo neurogenesis by targeted expression of atoh7 to Müller glia cells Lust, Katharina Sinn, Rebecca Pérez Saturnino, Alicia Centanin, Lázaro Wittbrodt, Joachim Development Stem Cells and Regeneration Regenerative responses in the vertebrate CNS depend on quiescent radial glia stem cells, which re-enter the cell cycle and eventually differentiate into neurons. The entry into the cell cycle and the differentiation into neurons are events of opposite nature, and therefore efforts to force quiescent radial glia into neurons require different factors. Here, we use fish to show that a single neurogenic factor, Atoh7, directs retinal radial glia (Müller glia, MG) into proliferation. The resulting neurogenic clusters differentiate in vivo into various retinal neurons. We use signaling reporters to demonstrate that the Atoh7-induced regeneration-like response of MG cells is mimicked by Notch, resembling the behavior of early progenitors during retinogenesis. Activation of Notch signaling in MG cells is sufficient to trigger proliferation and differentiation. Our results uncover a new role for Atoh7 as a universal neurogenic factor, and illustrate how signaling modules are re-employed in diverse contexts to trigger different biological responses. The Company of Biologists Ltd 2016-06-01 /pmc/articles/PMC4920165/ /pubmed/27068106 http://dx.doi.org/10.1242/dev.135905 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Stem Cells and Regeneration
Lust, Katharina
Sinn, Rebecca
Pérez Saturnino, Alicia
Centanin, Lázaro
Wittbrodt, Joachim
De novo neurogenesis by targeted expression of atoh7 to Müller glia cells
title De novo neurogenesis by targeted expression of atoh7 to Müller glia cells
title_full De novo neurogenesis by targeted expression of atoh7 to Müller glia cells
title_fullStr De novo neurogenesis by targeted expression of atoh7 to Müller glia cells
title_full_unstemmed De novo neurogenesis by targeted expression of atoh7 to Müller glia cells
title_short De novo neurogenesis by targeted expression of atoh7 to Müller glia cells
title_sort de novo neurogenesis by targeted expression of atoh7 to müller glia cells
topic Stem Cells and Regeneration
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920165/
https://www.ncbi.nlm.nih.gov/pubmed/27068106
http://dx.doi.org/10.1242/dev.135905
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