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Experience-dependent development of visual sensitivity in larval zebrafish

The zebrafish (Danio rerio) is a popular vertebrate model for studying visual development, especially at the larval stage. For many vertebrates, post-natal visual experience is essential to fine-tune visual development, but it is unknown how experience shapes larval zebrafish vision. Zebrafish swim...

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Autores principales: Xie, Jiaheng, Jusuf, Patricia R., Bui, Bang V., Goodbourn, Patrick T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908733/
https://www.ncbi.nlm.nih.gov/pubmed/31831839
http://dx.doi.org/10.1038/s41598-019-54958-6
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author Xie, Jiaheng
Jusuf, Patricia R.
Bui, Bang V.
Goodbourn, Patrick T.
author_facet Xie, Jiaheng
Jusuf, Patricia R.
Bui, Bang V.
Goodbourn, Patrick T.
author_sort Xie, Jiaheng
collection PubMed
description The zebrafish (Danio rerio) is a popular vertebrate model for studying visual development, especially at the larval stage. For many vertebrates, post-natal visual experience is essential to fine-tune visual development, but it is unknown how experience shapes larval zebrafish vision. Zebrafish swim with a moving texture; in the wild, this innate optomotor response (OMR) stabilises larvae in moving water, but it can be exploited in the laboratory to assess zebrafish visual function. Here, we compared spatial-frequency tuning inferred from OMR between visually naïve and experienced larvae from 5 to 7 days post-fertilisation. We also examined development of synaptic connections between neurons by quantifying post-synaptic density 95 (PSD-95) in larval retinae. PSD-95 is closely associated with N-methyl-D-aspartate (NMDA) receptors, the neurotransmitter-receptor proteins underlying experience-dependent visual development. We found that rather than following an experience-independent genetic programme, developmental changes in visual spatial-frequency tuning at the larval stage required visual experience. Exposure to motion evoking OMR yielded no greater improvement than exposure to static form, suggesting that increased sensitivity as indexed by OMR was driven not by motor practice but by visual experience itself. PSD-95 density varied with visual sensitivity, suggesting that experience may have up-regulated clustering of PSD-95 for synaptic maturation in visual development.
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spelling pubmed-69087332019-12-16 Experience-dependent development of visual sensitivity in larval zebrafish Xie, Jiaheng Jusuf, Patricia R. Bui, Bang V. Goodbourn, Patrick T. Sci Rep Article The zebrafish (Danio rerio) is a popular vertebrate model for studying visual development, especially at the larval stage. For many vertebrates, post-natal visual experience is essential to fine-tune visual development, but it is unknown how experience shapes larval zebrafish vision. Zebrafish swim with a moving texture; in the wild, this innate optomotor response (OMR) stabilises larvae in moving water, but it can be exploited in the laboratory to assess zebrafish visual function. Here, we compared spatial-frequency tuning inferred from OMR between visually naïve and experienced larvae from 5 to 7 days post-fertilisation. We also examined development of synaptic connections between neurons by quantifying post-synaptic density 95 (PSD-95) in larval retinae. PSD-95 is closely associated with N-methyl-D-aspartate (NMDA) receptors, the neurotransmitter-receptor proteins underlying experience-dependent visual development. We found that rather than following an experience-independent genetic programme, developmental changes in visual spatial-frequency tuning at the larval stage required visual experience. Exposure to motion evoking OMR yielded no greater improvement than exposure to static form, suggesting that increased sensitivity as indexed by OMR was driven not by motor practice but by visual experience itself. PSD-95 density varied with visual sensitivity, suggesting that experience may have up-regulated clustering of PSD-95 for synaptic maturation in visual development. Nature Publishing Group UK 2019-12-12 /pmc/articles/PMC6908733/ /pubmed/31831839 http://dx.doi.org/10.1038/s41598-019-54958-6 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
Xie, Jiaheng
Jusuf, Patricia R.
Bui, Bang V.
Goodbourn, Patrick T.
Experience-dependent development of visual sensitivity in larval zebrafish
title Experience-dependent development of visual sensitivity in larval zebrafish
title_full Experience-dependent development of visual sensitivity in larval zebrafish
title_fullStr Experience-dependent development of visual sensitivity in larval zebrafish
title_full_unstemmed Experience-dependent development of visual sensitivity in larval zebrafish
title_short Experience-dependent development of visual sensitivity in larval zebrafish
title_sort experience-dependent development of visual sensitivity in larval zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908733/
https://www.ncbi.nlm.nih.gov/pubmed/31831839
http://dx.doi.org/10.1038/s41598-019-54958-6
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