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Probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina
Retinal implants are used to replace lost photoreceptors in blind patients suffering from retinopathies such as retinitis pigmentosa. Patients wearing implants regain some rudimentary visual function. However, it is severely limited compared to normal vision because non-physiological stimulation str...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090015/ https://www.ncbi.nlm.nih.gov/pubmed/32251331 http://dx.doi.org/10.1038/s41598-020-61899-y |
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author | Höfling, Larissa Oesterle, Jonathan Berens, Philipp Zeck, Günther |
author_facet | Höfling, Larissa Oesterle, Jonathan Berens, Philipp Zeck, Günther |
author_sort | Höfling, Larissa |
collection | PubMed |
description | Retinal implants are used to replace lost photoreceptors in blind patients suffering from retinopathies such as retinitis pigmentosa. Patients wearing implants regain some rudimentary visual function. However, it is severely limited compared to normal vision because non-physiological stimulation strategies fail to selectively activate different retinal pathways at sufficient spatial and temporal resolution. The development of improved stimulation strategies is rendered difficult by the large space of potential stimuli. Here we systematically explore a subspace of potential stimuli by electrically stimulating healthy and blind mouse retina in epiretinal configuration using smooth Gaussian white noise delivered by a high-density CMOS-based microelectrode array. We identify linear filters of retinal ganglion cells (RGCs) by fitting a linear-nonlinear-Poisson (LNP) model. Our stimulus evokes spatially and temporally confined spiking responses in RGC which are accurately predicted by the LNP model. Furthermore, we find diverse shapes of linear filters in the linear stage of the model, suggesting diverse preferred electrical stimuli of RGCs. The linear filter base identified by our approach could provide a starting point of a model-guided search for improved stimuli for retinal prosthetics. |
format | Online Article Text |
id | pubmed-7090015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70900152020-03-26 Probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina Höfling, Larissa Oesterle, Jonathan Berens, Philipp Zeck, Günther Sci Rep Article Retinal implants are used to replace lost photoreceptors in blind patients suffering from retinopathies such as retinitis pigmentosa. Patients wearing implants regain some rudimentary visual function. However, it is severely limited compared to normal vision because non-physiological stimulation strategies fail to selectively activate different retinal pathways at sufficient spatial and temporal resolution. The development of improved stimulation strategies is rendered difficult by the large space of potential stimuli. Here we systematically explore a subspace of potential stimuli by electrically stimulating healthy and blind mouse retina in epiretinal configuration using smooth Gaussian white noise delivered by a high-density CMOS-based microelectrode array. We identify linear filters of retinal ganglion cells (RGCs) by fitting a linear-nonlinear-Poisson (LNP) model. Our stimulus evokes spatially and temporally confined spiking responses in RGC which are accurately predicted by the LNP model. Furthermore, we find diverse shapes of linear filters in the linear stage of the model, suggesting diverse preferred electrical stimuli of RGCs. The linear filter base identified by our approach could provide a starting point of a model-guided search for improved stimuli for retinal prosthetics. Nature Publishing Group UK 2020-03-23 /pmc/articles/PMC7090015/ /pubmed/32251331 http://dx.doi.org/10.1038/s41598-020-61899-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Höfling, Larissa Oesterle, Jonathan Berens, Philipp Zeck, Günther Probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina |
title | Probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina |
title_full | Probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina |
title_fullStr | Probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina |
title_full_unstemmed | Probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina |
title_short | Probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina |
title_sort | probing and predicting ganglion cell responses to smooth electrical stimulation in healthy and blind mouse retina |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090015/ https://www.ncbi.nlm.nih.gov/pubmed/32251331 http://dx.doi.org/10.1038/s41598-020-61899-y |
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