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A distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain
Saccades are rapid eye movements that redirect gaze. Their magnitudes and directions are tightly controlled by the oculomotor system, which is capable of generating conjugate, monocular, convergent and divergent saccades. Recent studies suggest a mainly monocular control of saccades in mammals, alth...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209155/ https://www.ncbi.nlm.nih.gov/pubmed/34135354 http://dx.doi.org/10.1038/s41598-021-90315-2 |
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author | Leyden, Claire Brysch, Christian Arrenberg, Aristides B. |
author_facet | Leyden, Claire Brysch, Christian Arrenberg, Aristides B. |
author_sort | Leyden, Claire |
collection | PubMed |
description | Saccades are rapid eye movements that redirect gaze. Their magnitudes and directions are tightly controlled by the oculomotor system, which is capable of generating conjugate, monocular, convergent and divergent saccades. Recent studies suggest a mainly monocular control of saccades in mammals, although the development of binocular control and the interaction of different functional populations is less well understood. For zebrafish, a well-established model in sensorimotor research, the nature of binocular control in this key oculomotor behavior is unknown. Here, we use the optokinetic response and calcium imaging to characterize how the developing zebrafish oculomotor system encodes the diverse repertoire of saccades. We find that neurons with phasic saccade-associated activity (putative burst neurons) are most frequent in dorsal regions of the hindbrain and show elements of both monocular and binocular encoding, revealing a mix of the response types originally hypothesized by Helmholtz and Hering. Additionally, we observed a certain degree of behavior-specific recruitment in individual neurons. Surprisingly, calcium activity is only weakly tuned to saccade size. Instead, saccade size is apparently controlled by a push–pull mechanism of opposing burst neuron populations. Our study reveals the basic layout of a developing vertebrate saccade system and provides a perspective into the evolution of the oculomotor system. |
format | Online Article Text |
id | pubmed-8209155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82091552021-06-17 A distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain Leyden, Claire Brysch, Christian Arrenberg, Aristides B. Sci Rep Article Saccades are rapid eye movements that redirect gaze. Their magnitudes and directions are tightly controlled by the oculomotor system, which is capable of generating conjugate, monocular, convergent and divergent saccades. Recent studies suggest a mainly monocular control of saccades in mammals, although the development of binocular control and the interaction of different functional populations is less well understood. For zebrafish, a well-established model in sensorimotor research, the nature of binocular control in this key oculomotor behavior is unknown. Here, we use the optokinetic response and calcium imaging to characterize how the developing zebrafish oculomotor system encodes the diverse repertoire of saccades. We find that neurons with phasic saccade-associated activity (putative burst neurons) are most frequent in dorsal regions of the hindbrain and show elements of both monocular and binocular encoding, revealing a mix of the response types originally hypothesized by Helmholtz and Hering. Additionally, we observed a certain degree of behavior-specific recruitment in individual neurons. Surprisingly, calcium activity is only weakly tuned to saccade size. Instead, saccade size is apparently controlled by a push–pull mechanism of opposing burst neuron populations. Our study reveals the basic layout of a developing vertebrate saccade system and provides a perspective into the evolution of the oculomotor system. Nature Publishing Group UK 2021-06-16 /pmc/articles/PMC8209155/ /pubmed/34135354 http://dx.doi.org/10.1038/s41598-021-90315-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Leyden, Claire Brysch, Christian Arrenberg, Aristides B. A distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain |
title | A distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain |
title_full | A distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain |
title_fullStr | A distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain |
title_full_unstemmed | A distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain |
title_short | A distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain |
title_sort | distributed saccade-associated network encodes high velocity conjugate and monocular eye movements in the zebrafish hindbrain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209155/ https://www.ncbi.nlm.nih.gov/pubmed/34135354 http://dx.doi.org/10.1038/s41598-021-90315-2 |
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