miRNAs and Müller Glia Reprogramming During Retina Regeneration

The use of model systems that are capable of robust, spontaneous retina regeneration has allowed for the identification of genetic pathways and components that are required for retina regeneration. Complemented by mouse models in which retina regeneration can be induced after forced expression of ke...

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Main Authors: Gregory J. Konar, Claire Ferguson, Zachary Flickinger, Matthew R. Kent, James G. Patton
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-01-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2020.632632/full
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spelling doaj-41c0f6d1289f4c27b02528812a0590352021-01-18T05:22:07ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-01-01810.3389/fcell.2020.632632632632miRNAs and Müller Glia Reprogramming During Retina RegenerationGregory J. KonarClaire FergusonZachary FlickingerMatthew R. KentJames G. PattonThe use of model systems that are capable of robust, spontaneous retina regeneration has allowed for the identification of genetic pathways and components that are required for retina regeneration. Complemented by mouse models in which retina regeneration can be induced after forced expression of key factors, altered chromatin accessibility, or inhibition of kinase/signaling cascades, a clearer picture of the key regulatory events that control retina regeneration is emerging. In all cases, Müller glia (MG) serve as an adult retinal stem cell that must be reprogrammed to allow for regeneration, with the end goal being to understand why regenerative pathways are blocked in mammals, but spontaneous in other vertebrates such as zebrafish. miRNAs have emerged as key gene regulatory molecules that control both development and regeneration in vertebrates. Here, we focus on a small subset of miRNAs that control MG reprogramming during retina regeneration and have the potential to serve as therapeutic targets for treatment of visual disorders and damage.https://www.frontiersin.org/articles/10.3389/fcell.2020.632632/fullmiRNAMüller gliaretinaregenerationzebrafish
collection DOAJ
language English
format Article
sources DOAJ
author Gregory J. Konar
Claire Ferguson
Zachary Flickinger
Matthew R. Kent
James G. Patton
spellingShingle Gregory J. Konar
Claire Ferguson
Zachary Flickinger
Matthew R. Kent
James G. Patton
miRNAs and Müller Glia Reprogramming During Retina Regeneration
Frontiers in Cell and Developmental Biology
miRNA
Müller glia
retina
regeneration
zebrafish
author_facet Gregory J. Konar
Claire Ferguson
Zachary Flickinger
Matthew R. Kent
James G. Patton
author_sort Gregory J. Konar
title miRNAs and Müller Glia Reprogramming During Retina Regeneration
title_short miRNAs and Müller Glia Reprogramming During Retina Regeneration
title_full miRNAs and Müller Glia Reprogramming During Retina Regeneration
title_fullStr miRNAs and Müller Glia Reprogramming During Retina Regeneration
title_full_unstemmed miRNAs and Müller Glia Reprogramming During Retina Regeneration
title_sort mirnas and müller glia reprogramming during retina regeneration
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2021-01-01
description The use of model systems that are capable of robust, spontaneous retina regeneration has allowed for the identification of genetic pathways and components that are required for retina regeneration. Complemented by mouse models in which retina regeneration can be induced after forced expression of key factors, altered chromatin accessibility, or inhibition of kinase/signaling cascades, a clearer picture of the key regulatory events that control retina regeneration is emerging. In all cases, Müller glia (MG) serve as an adult retinal stem cell that must be reprogrammed to allow for regeneration, with the end goal being to understand why regenerative pathways are blocked in mammals, but spontaneous in other vertebrates such as zebrafish. miRNAs have emerged as key gene regulatory molecules that control both development and regeneration in vertebrates. Here, we focus on a small subset of miRNAs that control MG reprogramming during retina regeneration and have the potential to serve as therapeutic targets for treatment of visual disorders and damage.
topic miRNA
Müller glia
retina
regeneration
zebrafish
url https://www.frontiersin.org/articles/10.3389/fcell.2020.632632/full
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AT zacharyflickinger mirnasandmullergliareprogrammingduringretinaregeneration
AT matthewrkent mirnasandmullergliareprogrammingduringretinaregeneration
AT jamesgpatton mirnasandmullergliareprogrammingduringretinaregeneration
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