Retinal Stem/Progenitor Cells Derived From Adult Müller Glia for the Treatment of Retinal Degeneration

Over the past two decades, progress in our understanding of glial function has been revolutionary. Within the retina, a subset of glial cells termed the “Müller glia (MG),” have been demonstrated to play key roles in retinal homeostasis, structure and metabolism. Additionally, MG have also been show...

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Main Authors: Lay Khoon Too, Matthew P. Simunovic
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.2021.749131/full
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spelling doaj-ad82ade212f042aab1dcaec1e8fdb5282021-09-29T05:33:11ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-09-01910.3389/fcell.2021.749131749131Retinal Stem/Progenitor Cells Derived From Adult Müller Glia for the Treatment of Retinal DegenerationLay Khoon Too0Matthew P. Simunovic1Matthew P. Simunovic2Save Sight Institute, The University of Sydney, Sydney, NSW, AustraliaSave Sight Institute, The University of Sydney, Sydney, NSW, AustraliaSydney Eye Hospital, Sydney, NSW, AustraliaOver the past two decades, progress in our understanding of glial function has been revolutionary. Within the retina, a subset of glial cells termed the “Müller glia (MG),” have been demonstrated to play key roles in retinal homeostasis, structure and metabolism. Additionally, MG have also been shown to possess the regenerative capacity that varies across species. In teleost fish, MG respond to injury by reprogramming into stem-like cells capable of regenerating lost tissue. The expression of stem/progenitor cell markers has been demonstrated broadly in mammalian MG, including human MG, but their in vivo regenerative capacity appears evolutionarily limited. Advances in stem cell therapy have progressively elucidated critical mechanisms underlying innate MG reprogramming in teleost fish, which have shown promising results when applied to rodents. Furthermore, when cultured ex vivo, MG from mammals can differentiate into several retina cell types. In this review, we will explore the reparative and regenerative potential of MG in cellular therapy approaches, and outline our current understanding of embryonic retinal development, the stem-cell potential of MG in adult vertebrate retina (including human), and microenvironmental cues that guide MG reprogramming.https://www.frontiersin.org/articles/10.3389/fcell.2021.749131/fullMüller gliaretinal degenerationstem-cell therapyregenerationreprogramming
collection DOAJ
language English
format Article
sources DOAJ
author Lay Khoon Too
Matthew P. Simunovic
Matthew P. Simunovic
spellingShingle Lay Khoon Too
Matthew P. Simunovic
Matthew P. Simunovic
Retinal Stem/Progenitor Cells Derived From Adult Müller Glia for the Treatment of Retinal Degeneration
Frontiers in Cell and Developmental Biology
Müller glia
retinal degeneration
stem-cell therapy
regeneration
reprogramming
author_facet Lay Khoon Too
Matthew P. Simunovic
Matthew P. Simunovic
author_sort Lay Khoon Too
title Retinal Stem/Progenitor Cells Derived From Adult Müller Glia for the Treatment of Retinal Degeneration
title_short Retinal Stem/Progenitor Cells Derived From Adult Müller Glia for the Treatment of Retinal Degeneration
title_full Retinal Stem/Progenitor Cells Derived From Adult Müller Glia for the Treatment of Retinal Degeneration
title_fullStr Retinal Stem/Progenitor Cells Derived From Adult Müller Glia for the Treatment of Retinal Degeneration
title_full_unstemmed Retinal Stem/Progenitor Cells Derived From Adult Müller Glia for the Treatment of Retinal Degeneration
title_sort retinal stem/progenitor cells derived from adult müller glia for the treatment of retinal degeneration
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2021-09-01
description Over the past two decades, progress in our understanding of glial function has been revolutionary. Within the retina, a subset of glial cells termed the “Müller glia (MG),” have been demonstrated to play key roles in retinal homeostasis, structure and metabolism. Additionally, MG have also been shown to possess the regenerative capacity that varies across species. In teleost fish, MG respond to injury by reprogramming into stem-like cells capable of regenerating lost tissue. The expression of stem/progenitor cell markers has been demonstrated broadly in mammalian MG, including human MG, but their in vivo regenerative capacity appears evolutionarily limited. Advances in stem cell therapy have progressively elucidated critical mechanisms underlying innate MG reprogramming in teleost fish, which have shown promising results when applied to rodents. Furthermore, when cultured ex vivo, MG from mammals can differentiate into several retina cell types. In this review, we will explore the reparative and regenerative potential of MG in cellular therapy approaches, and outline our current understanding of embryonic retinal development, the stem-cell potential of MG in adult vertebrate retina (including human), and microenvironmental cues that guide MG reprogramming.
topic Müller glia
retinal degeneration
stem-cell therapy
regeneration
reprogramming
url https://www.frontiersin.org/articles/10.3389/fcell.2021.749131/full
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