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Response Latency Tuning by Retinal Circuits Modulates Signal Efficiency

In the visual system, retinal ganglion cells (RGCs) of various subtypes encode preprocessed photoreceptor signals into a spike output which is then transmitted towards the brain through parallel feature pathways. Spike timing determines how each feature signal contributes to the output of downstream...

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Autores principales: Tengölics, Ádám Jonatán, Szarka, Gergely, Ganczer, Alma, Szabó-Meleg, Edina, Nyitrai, Miklós, Kovács-Öller, Tamás, Völgyi, Béla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806000/
https://www.ncbi.nlm.nih.gov/pubmed/31641196
http://dx.doi.org/10.1038/s41598-019-51756-y
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author Tengölics, Ádám Jonatán
Szarka, Gergely
Ganczer, Alma
Szabó-Meleg, Edina
Nyitrai, Miklós
Kovács-Öller, Tamás
Völgyi, Béla
author_facet Tengölics, Ádám Jonatán
Szarka, Gergely
Ganczer, Alma
Szabó-Meleg, Edina
Nyitrai, Miklós
Kovács-Öller, Tamás
Völgyi, Béla
author_sort Tengölics, Ádám Jonatán
collection PubMed
description In the visual system, retinal ganglion cells (RGCs) of various subtypes encode preprocessed photoreceptor signals into a spike output which is then transmitted towards the brain through parallel feature pathways. Spike timing determines how each feature signal contributes to the output of downstream neurons in visual brain centers, thereby influencing efficiency in visual perception. In this study, we demonstrate a marked population-wide variability in RGC response latency that is independent of trial-to-trial variability and recording approach. RGC response latencies to simple visual stimuli vary considerably in a heterogenous cell population but remain reliable when RGCs of a single subtype are compared. This subtype specificity, however, vanishes when the retinal circuitry is bypassed via direct RGC electrical stimulation. This suggests that latency is primarily determined by the signaling speed through retinal pathways that provide subtype specific inputs to RGCs. In addition, response latency is significantly altered when GABA inhibition or gap junction signaling is disturbed, which further supports the key role of retinal microcircuits in latency tuning. Finally, modulation of stimulus parameters affects individual RGC response delays considerably. Based on these findings, we hypothesize that retinal microcircuits fine-tune RGC response latency, which in turn determines the context-dependent weighing of each signal and its contribution to visual perception.
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spelling pubmed-68060002019-10-24 Response Latency Tuning by Retinal Circuits Modulates Signal Efficiency Tengölics, Ádám Jonatán Szarka, Gergely Ganczer, Alma Szabó-Meleg, Edina Nyitrai, Miklós Kovács-Öller, Tamás Völgyi, Béla Sci Rep Article In the visual system, retinal ganglion cells (RGCs) of various subtypes encode preprocessed photoreceptor signals into a spike output which is then transmitted towards the brain through parallel feature pathways. Spike timing determines how each feature signal contributes to the output of downstream neurons in visual brain centers, thereby influencing efficiency in visual perception. In this study, we demonstrate a marked population-wide variability in RGC response latency that is independent of trial-to-trial variability and recording approach. RGC response latencies to simple visual stimuli vary considerably in a heterogenous cell population but remain reliable when RGCs of a single subtype are compared. This subtype specificity, however, vanishes when the retinal circuitry is bypassed via direct RGC electrical stimulation. This suggests that latency is primarily determined by the signaling speed through retinal pathways that provide subtype specific inputs to RGCs. In addition, response latency is significantly altered when GABA inhibition or gap junction signaling is disturbed, which further supports the key role of retinal microcircuits in latency tuning. Finally, modulation of stimulus parameters affects individual RGC response delays considerably. Based on these findings, we hypothesize that retinal microcircuits fine-tune RGC response latency, which in turn determines the context-dependent weighing of each signal and its contribution to visual perception. Nature Publishing Group UK 2019-10-22 /pmc/articles/PMC6806000/ /pubmed/31641196 http://dx.doi.org/10.1038/s41598-019-51756-y Text en © The Author(s) 2019 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
Tengölics, Ádám Jonatán
Szarka, Gergely
Ganczer, Alma
Szabó-Meleg, Edina
Nyitrai, Miklós
Kovács-Öller, Tamás
Völgyi, Béla
Response Latency Tuning by Retinal Circuits Modulates Signal Efficiency
title Response Latency Tuning by Retinal Circuits Modulates Signal Efficiency
title_full Response Latency Tuning by Retinal Circuits Modulates Signal Efficiency
title_fullStr Response Latency Tuning by Retinal Circuits Modulates Signal Efficiency
title_full_unstemmed Response Latency Tuning by Retinal Circuits Modulates Signal Efficiency
title_short Response Latency Tuning by Retinal Circuits Modulates Signal Efficiency
title_sort response latency tuning by retinal circuits modulates signal efficiency
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806000/
https://www.ncbi.nlm.nih.gov/pubmed/31641196
http://dx.doi.org/10.1038/s41598-019-51756-y
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