A survey of retinal remodeling

Up to 15 years ago, bibliographic searches based on keywords such as photoreceptor degeneration, inner retina or photoreceptor degeneration, second order neurons returned only a handful of papers, as the field was dominated by the general assumption that retinal degeneration had direct effects on th...

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Main Author: Enrica eStrettoi
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-12-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2015.00494/full
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spelling doaj-da8b41cd8ecd4124afabde5966c5d9dc2020-11-24T22:47:15ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022015-12-01910.3389/fncel.2015.00494172336A survey of retinal remodelingEnrica eStrettoi0Italian National Research Council, CNR. Neuroscience InstituteUp to 15 years ago, bibliographic searches based on keywords such as photoreceptor degeneration, inner retina or photoreceptor degeneration, second order neurons returned only a handful of papers, as the field was dominated by the general assumption that retinal degeneration had direct effects on the sole populations of rods and cones. Since then, a number of studies have been dedicated to understanding the process of gradual morphological, molecular and functional changes arising among cells located in the inner retina (comprising neurons, glia and blood vessels), that is to say beyond photoreceptors. General aspects of this progression of biological rearrangements, now referred to as remodeling, were revealed and demonstrated to accompany consistently photoreceptor loss, independently from the underlying cause of degeneration. Recurrent features of remodeling are summarized here, to provide a general frame for to the various analytical descriptions and reviews provided by the articles in the issue (among others, see Stasheff; Goo et al., Puthussery et al.; Fernández-Sánchez et al.; Euler and Schubert; Jones et al.; this issue).http://journal.frontiersin.org/Journal/10.3389/fncel.2015.00494/fullRetinitis PigmentosaBipolar cellganglion cellMGluR6retinal glia
collection DOAJ
language English
format Article
sources DOAJ
author Enrica eStrettoi
spellingShingle Enrica eStrettoi
A survey of retinal remodeling
Frontiers in Cellular Neuroscience
Retinitis Pigmentosa
Bipolar cell
ganglion cell
MGluR6
retinal glia
author_facet Enrica eStrettoi
author_sort Enrica eStrettoi
title A survey of retinal remodeling
title_short A survey of retinal remodeling
title_full A survey of retinal remodeling
title_fullStr A survey of retinal remodeling
title_full_unstemmed A survey of retinal remodeling
title_sort survey of retinal remodeling
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2015-12-01
description Up to 15 years ago, bibliographic searches based on keywords such as photoreceptor degeneration, inner retina or photoreceptor degeneration, second order neurons returned only a handful of papers, as the field was dominated by the general assumption that retinal degeneration had direct effects on the sole populations of rods and cones. Since then, a number of studies have been dedicated to understanding the process of gradual morphological, molecular and functional changes arising among cells located in the inner retina (comprising neurons, glia and blood vessels), that is to say beyond photoreceptors. General aspects of this progression of biological rearrangements, now referred to as remodeling, were revealed and demonstrated to accompany consistently photoreceptor loss, independently from the underlying cause of degeneration. Recurrent features of remodeling are summarized here, to provide a general frame for to the various analytical descriptions and reviews provided by the articles in the issue (among others, see Stasheff; Goo et al., Puthussery et al.; Fernández-Sánchez et al.; Euler and Schubert; Jones et al.; this issue).
topic Retinitis Pigmentosa
Bipolar cell
ganglion cell
MGluR6
retinal glia
url http://journal.frontiersin.org/Journal/10.3389/fncel.2015.00494/full
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