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A biophysical model explains the spontaneous bursting behavior in the developing retina
During early development, waves of activity propagate across the retina and play a key role in the proper wiring of the early visual system. During a particular phase of the retina development (stage II) these waves are triggered by a transient network of neurons, called Starburst Amacrine Cells (SA...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372601/ https://www.ncbi.nlm.nih.gov/pubmed/30755684 http://dx.doi.org/10.1038/s41598-018-38299-4 |
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author | Matzakos-Karvouniari, Dora Gil, Lionel Orendorff, Elaine Marre, Olivier Picaud, Serge Cessac, Bruno |
author_facet | Matzakos-Karvouniari, Dora Gil, Lionel Orendorff, Elaine Marre, Olivier Picaud, Serge Cessac, Bruno |
author_sort | Matzakos-Karvouniari, Dora |
collection | PubMed |
description | During early development, waves of activity propagate across the retina and play a key role in the proper wiring of the early visual system. During a particular phase of the retina development (stage II) these waves are triggered by a transient network of neurons, called Starburst Amacrine Cells (SACs), showing a bursting activity which disappears upon further maturation. The underlying mechanisms of the spontaneous bursting and the transient excitability of immature SACs are not completely clear yet. While several models have attempted to reproduce retinal waves, none of them is able to mimic the rhythmic autonomous bursting of individual SACs and reveal how these cells change their intrinsic properties during development. Here, we introduce a mathematical model, grounded on biophysics, which enables us to reproduce the bursting activity of SACs and to propose a plausible, generic and robust, mechanism that generates it. The core parameters controlling repetitive firing are fast depolarizing V-gated calcium channels and hyperpolarizing V-gated potassium channels. The quiescent phase of bursting is controlled by a slow after hyperpolarization (sAHP), mediated by calcium-dependent potassium channels. Based on a bifurcation analysis we show how biophysical parameters, regulating calcium and potassium activity, control the spontaneously occurring fast oscillatory activity followed by long refractory periods in individual SACs. We make a testable experimental prediction on the role of voltage-dependent potassium channels on the excitability properties of SACs and on the evolution of this excitability along development. We also propose an explanation on how SACs can exhibit a large variability in their bursting periods, as observed experimentally within a SACs network as well as across different species, yet based on a simple, unique, mechanism. As we discuss, these observations at the cellular level have a deep impact on the retinal waves description. |
format | Online Article Text |
id | pubmed-6372601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63726012019-02-19 A biophysical model explains the spontaneous bursting behavior in the developing retina Matzakos-Karvouniari, Dora Gil, Lionel Orendorff, Elaine Marre, Olivier Picaud, Serge Cessac, Bruno Sci Rep Article During early development, waves of activity propagate across the retina and play a key role in the proper wiring of the early visual system. During a particular phase of the retina development (stage II) these waves are triggered by a transient network of neurons, called Starburst Amacrine Cells (SACs), showing a bursting activity which disappears upon further maturation. The underlying mechanisms of the spontaneous bursting and the transient excitability of immature SACs are not completely clear yet. While several models have attempted to reproduce retinal waves, none of them is able to mimic the rhythmic autonomous bursting of individual SACs and reveal how these cells change their intrinsic properties during development. Here, we introduce a mathematical model, grounded on biophysics, which enables us to reproduce the bursting activity of SACs and to propose a plausible, generic and robust, mechanism that generates it. The core parameters controlling repetitive firing are fast depolarizing V-gated calcium channels and hyperpolarizing V-gated potassium channels. The quiescent phase of bursting is controlled by a slow after hyperpolarization (sAHP), mediated by calcium-dependent potassium channels. Based on a bifurcation analysis we show how biophysical parameters, regulating calcium and potassium activity, control the spontaneously occurring fast oscillatory activity followed by long refractory periods in individual SACs. We make a testable experimental prediction on the role of voltage-dependent potassium channels on the excitability properties of SACs and on the evolution of this excitability along development. We also propose an explanation on how SACs can exhibit a large variability in their bursting periods, as observed experimentally within a SACs network as well as across different species, yet based on a simple, unique, mechanism. As we discuss, these observations at the cellular level have a deep impact on the retinal waves description. Nature Publishing Group UK 2019-02-12 /pmc/articles/PMC6372601/ /pubmed/30755684 http://dx.doi.org/10.1038/s41598-018-38299-4 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 Matzakos-Karvouniari, Dora Gil, Lionel Orendorff, Elaine Marre, Olivier Picaud, Serge Cessac, Bruno A biophysical model explains the spontaneous bursting behavior in the developing retina |
title | A biophysical model explains the spontaneous bursting behavior in the developing retina |
title_full | A biophysical model explains the spontaneous bursting behavior in the developing retina |
title_fullStr | A biophysical model explains the spontaneous bursting behavior in the developing retina |
title_full_unstemmed | A biophysical model explains the spontaneous bursting behavior in the developing retina |
title_short | A biophysical model explains the spontaneous bursting behavior in the developing retina |
title_sort | biophysical model explains the spontaneous bursting behavior in the developing retina |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372601/ https://www.ncbi.nlm.nih.gov/pubmed/30755684 http://dx.doi.org/10.1038/s41598-018-38299-4 |
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