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Electrical coupling between A17 cells enhances reciprocal inhibitory feedback to rod bipolar cells
A17 amacrine cells are an important part of the scotopic pathway. Their synaptic varicosities receive glutamatergic inputs from rod bipolar cells (RBC) and release GABA onto the same RBC terminal, forming a reciprocal feedback that shapes RBC depolarization. Here, using patch-clamp recordings, we ch...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814567/ https://www.ncbi.nlm.nih.gov/pubmed/29449585 http://dx.doi.org/10.1038/s41598-018-21119-0 |
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author | Elgueta, Claudio Leroy, Felix Vielma, Alex H. Schmachtenberg, Oliver Palacios, Adrian G. |
author_facet | Elgueta, Claudio Leroy, Felix Vielma, Alex H. Schmachtenberg, Oliver Palacios, Adrian G. |
author_sort | Elgueta, Claudio |
collection | PubMed |
description | A17 amacrine cells are an important part of the scotopic pathway. Their synaptic varicosities receive glutamatergic inputs from rod bipolar cells (RBC) and release GABA onto the same RBC terminal, forming a reciprocal feedback that shapes RBC depolarization. Here, using patch-clamp recordings, we characterized electrical coupling between A17 cells of the rat retina and report the presence of strongly interconnected and non-coupled A17 cells. In coupled A17 cells, evoked currents preferentially flow out of the cell through GJs and cross-synchronization of presynaptic signals in a pair of A17 cells is correlated to their coupling degree. Moreover, we demonstrate that stimulation of one A17 cell can induce electrical and calcium transients in neighboring A17 cells, thus confirming a functional flow of information through electrical synapses in the A17 coupled network. Finally, blocking GJs caused a strong decrease in the amplitude of the inhibitory feedback onto RBCs. We therefore propose that electrical coupling between A17 cells enhances feedback onto RBCs by synchronizing and facilitating GABA release from inhibitory varicosities surrounding each RBC axon terminal. GJs between A17 cells are therefore critical in shaping the visual flow through the scotopic pathway. |
format | Online Article Text |
id | pubmed-5814567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58145672018-02-21 Electrical coupling between A17 cells enhances reciprocal inhibitory feedback to rod bipolar cells Elgueta, Claudio Leroy, Felix Vielma, Alex H. Schmachtenberg, Oliver Palacios, Adrian G. Sci Rep Article A17 amacrine cells are an important part of the scotopic pathway. Their synaptic varicosities receive glutamatergic inputs from rod bipolar cells (RBC) and release GABA onto the same RBC terminal, forming a reciprocal feedback that shapes RBC depolarization. Here, using patch-clamp recordings, we characterized electrical coupling between A17 cells of the rat retina and report the presence of strongly interconnected and non-coupled A17 cells. In coupled A17 cells, evoked currents preferentially flow out of the cell through GJs and cross-synchronization of presynaptic signals in a pair of A17 cells is correlated to their coupling degree. Moreover, we demonstrate that stimulation of one A17 cell can induce electrical and calcium transients in neighboring A17 cells, thus confirming a functional flow of information through electrical synapses in the A17 coupled network. Finally, blocking GJs caused a strong decrease in the amplitude of the inhibitory feedback onto RBCs. We therefore propose that electrical coupling between A17 cells enhances feedback onto RBCs by synchronizing and facilitating GABA release from inhibitory varicosities surrounding each RBC axon terminal. GJs between A17 cells are therefore critical in shaping the visual flow through the scotopic pathway. Nature Publishing Group UK 2018-02-15 /pmc/articles/PMC5814567/ /pubmed/29449585 http://dx.doi.org/10.1038/s41598-018-21119-0 Text en © The Author(s) 2018 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 Elgueta, Claudio Leroy, Felix Vielma, Alex H. Schmachtenberg, Oliver Palacios, Adrian G. Electrical coupling between A17 cells enhances reciprocal inhibitory feedback to rod bipolar cells |
title | Electrical coupling between A17 cells enhances reciprocal inhibitory feedback to rod bipolar cells |
title_full | Electrical coupling between A17 cells enhances reciprocal inhibitory feedback to rod bipolar cells |
title_fullStr | Electrical coupling between A17 cells enhances reciprocal inhibitory feedback to rod bipolar cells |
title_full_unstemmed | Electrical coupling between A17 cells enhances reciprocal inhibitory feedback to rod bipolar cells |
title_short | Electrical coupling between A17 cells enhances reciprocal inhibitory feedback to rod bipolar cells |
title_sort | electrical coupling between a17 cells enhances reciprocal inhibitory feedback to rod bipolar cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814567/ https://www.ncbi.nlm.nih.gov/pubmed/29449585 http://dx.doi.org/10.1038/s41598-018-21119-0 |
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