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Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum

BACKGROUND: The processing of optic flow in the pretectum/accessory optic system allows animals to stabilize retinal images by executing compensatory optokinetic and optomotor behavior. The success of this behavior depends on the integration of information from both eyes to unequivocally identify al...

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Autores principales: Wang, Kun, Hinz, Julian, Haikala, Väinö, Reiff, Dierk F., Arrenberg, Aristides B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441171/
https://www.ncbi.nlm.nih.gov/pubmed/30925897
http://dx.doi.org/10.1186/s12915-019-0648-2
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author Wang, Kun
Hinz, Julian
Haikala, Väinö
Reiff, Dierk F.
Arrenberg, Aristides B.
author_facet Wang, Kun
Hinz, Julian
Haikala, Väinö
Reiff, Dierk F.
Arrenberg, Aristides B.
author_sort Wang, Kun
collection PubMed
description BACKGROUND: The processing of optic flow in the pretectum/accessory optic system allows animals to stabilize retinal images by executing compensatory optokinetic and optomotor behavior. The success of this behavior depends on the integration of information from both eyes to unequivocally identify all possible translational or rotational directions of motion. However, it is still unknown whether the precise direction of ego-motion is already identified in the zebrafish pretectum or later in downstream premotor areas. RESULTS: Here, we show that the zebrafish pretectum and tectum each contain four populations of motion-sensitive direction-selective (DS) neurons, with each population encoding a different preferred direction upon monocular stimulation. In contrast, binocular stimulation revealed the existence of pretectal and tectal neurons that are specifically tuned to only one of the many possible combinations of monocular motion, suggesting that further downstream sensory processing might not be needed to instruct appropriate optokinetic and optomotor behavior. CONCLUSION: Our results suggest that local, task-specific pretectal circuits process DS retinal inputs and carry out the binocular sensory computations necessary for optokinetic and optomotor behavior. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0648-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-64411712019-04-11 Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum Wang, Kun Hinz, Julian Haikala, Väinö Reiff, Dierk F. Arrenberg, Aristides B. BMC Biol Research Article BACKGROUND: The processing of optic flow in the pretectum/accessory optic system allows animals to stabilize retinal images by executing compensatory optokinetic and optomotor behavior. The success of this behavior depends on the integration of information from both eyes to unequivocally identify all possible translational or rotational directions of motion. However, it is still unknown whether the precise direction of ego-motion is already identified in the zebrafish pretectum or later in downstream premotor areas. RESULTS: Here, we show that the zebrafish pretectum and tectum each contain four populations of motion-sensitive direction-selective (DS) neurons, with each population encoding a different preferred direction upon monocular stimulation. In contrast, binocular stimulation revealed the existence of pretectal and tectal neurons that are specifically tuned to only one of the many possible combinations of monocular motion, suggesting that further downstream sensory processing might not be needed to instruct appropriate optokinetic and optomotor behavior. CONCLUSION: Our results suggest that local, task-specific pretectal circuits process DS retinal inputs and carry out the binocular sensory computations necessary for optokinetic and optomotor behavior. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0648-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-29 /pmc/articles/PMC6441171/ /pubmed/30925897 http://dx.doi.org/10.1186/s12915-019-0648-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wang, Kun
Hinz, Julian
Haikala, Väinö
Reiff, Dierk F.
Arrenberg, Aristides B.
Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum
title Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum
title_full Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum
title_fullStr Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum
title_full_unstemmed Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum
title_short Selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum
title_sort selective processing of all rotational and translational optic flow directions in the zebrafish pretectum and tectum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441171/
https://www.ncbi.nlm.nih.gov/pubmed/30925897
http://dx.doi.org/10.1186/s12915-019-0648-2
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