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Differences in the spatial fidelity of evoked and spontaneous signals in the degenerating retina
Vision restoration strategies aim to reestablish vision by replacing the function of lost photoreceptors with optoelectronic hardware or through gene therapy. One complication to these approaches is that retinal circuitry undergoes remodeling after photoreceptor loss. Circuit remodeling following pe...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676928/ https://www.ncbi.nlm.nih.gov/pubmed/36419935 http://dx.doi.org/10.3389/fncel.2022.1040090 |
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author | Carleton, Maya Oesch, Nicholas W. |
author_facet | Carleton, Maya Oesch, Nicholas W. |
author_sort | Carleton, Maya |
collection | PubMed |
description | Vision restoration strategies aim to reestablish vision by replacing the function of lost photoreceptors with optoelectronic hardware or through gene therapy. One complication to these approaches is that retinal circuitry undergoes remodeling after photoreceptor loss. Circuit remodeling following perturbation is ubiquitous in the nervous system and understanding these changes is crucial for treating neurodegeneration. Spontaneous oscillations that arise during retinal degeneration have been well-studied, however, other changes in the spatiotemporal processing of evoked and spontaneous activity have received less attention. Here we use subretinal electrical stimulation to measure the spatial and temporal spread of both spontaneous and evoked activity during retinal degeneration. We found that electrical stimulation synchronizes spontaneous oscillatory activity, over space and through time, thus leading to increased correlations in ganglion cell activity. Intriguingly, we found that spatial selectivity was maintained in rd10 retina for evoked responses, with spatial receptive fields comparable to wt retina. These findings indicate that different biophysical mechanisms are involved in mediating feed forward excitation, and the lateral spread of spontaneous activity in the rd10 retina, lending support toward the possibility of high-resolution vision restoration. |
format | Online Article Text |
id | pubmed-9676928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96769282022-11-22 Differences in the spatial fidelity of evoked and spontaneous signals in the degenerating retina Carleton, Maya Oesch, Nicholas W. Front Cell Neurosci Neuroscience Vision restoration strategies aim to reestablish vision by replacing the function of lost photoreceptors with optoelectronic hardware or through gene therapy. One complication to these approaches is that retinal circuitry undergoes remodeling after photoreceptor loss. Circuit remodeling following perturbation is ubiquitous in the nervous system and understanding these changes is crucial for treating neurodegeneration. Spontaneous oscillations that arise during retinal degeneration have been well-studied, however, other changes in the spatiotemporal processing of evoked and spontaneous activity have received less attention. Here we use subretinal electrical stimulation to measure the spatial and temporal spread of both spontaneous and evoked activity during retinal degeneration. We found that electrical stimulation synchronizes spontaneous oscillatory activity, over space and through time, thus leading to increased correlations in ganglion cell activity. Intriguingly, we found that spatial selectivity was maintained in rd10 retina for evoked responses, with spatial receptive fields comparable to wt retina. These findings indicate that different biophysical mechanisms are involved in mediating feed forward excitation, and the lateral spread of spontaneous activity in the rd10 retina, lending support toward the possibility of high-resolution vision restoration. Frontiers Media S.A. 2022-11-07 /pmc/articles/PMC9676928/ /pubmed/36419935 http://dx.doi.org/10.3389/fncel.2022.1040090 Text en Copyright © 2022 Carleton and Oesch. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Carleton, Maya Oesch, Nicholas W. Differences in the spatial fidelity of evoked and spontaneous signals in the degenerating retina |
title | Differences in the spatial fidelity of evoked and spontaneous signals in the degenerating retina |
title_full | Differences in the spatial fidelity of evoked and spontaneous signals in the degenerating retina |
title_fullStr | Differences in the spatial fidelity of evoked and spontaneous signals in the degenerating retina |
title_full_unstemmed | Differences in the spatial fidelity of evoked and spontaneous signals in the degenerating retina |
title_short | Differences in the spatial fidelity of evoked and spontaneous signals in the degenerating retina |
title_sort | differences in the spatial fidelity of evoked and spontaneous signals in the degenerating retina |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676928/ https://www.ncbi.nlm.nih.gov/pubmed/36419935 http://dx.doi.org/10.3389/fncel.2022.1040090 |
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