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Zebrafish Retinal Ganglion Cells Asymmetrically Encode Spectral and Temporal Information across Visual Space

In vertebrate vision, the tetrachromatic larval zebrafish permits non-invasive monitoring and manipulating of neural activity across the nervous system in vivo during ongoing behavior. However, despite a perhaps unparalleled understanding of links between zebrafish brain circuits and visual behavior...

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Autores principales: Zhou, Mingyi, Bear, John, Roberts, Paul A., Janiak, Filip K., Semmelhack, Julie, Yoshimatsu, Takeshi, Baden, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416113/
https://www.ncbi.nlm.nih.gov/pubmed/32531283
http://dx.doi.org/10.1016/j.cub.2020.05.055
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author Zhou, Mingyi
Bear, John
Roberts, Paul A.
Janiak, Filip K.
Semmelhack, Julie
Yoshimatsu, Takeshi
Baden, Tom
author_facet Zhou, Mingyi
Bear, John
Roberts, Paul A.
Janiak, Filip K.
Semmelhack, Julie
Yoshimatsu, Takeshi
Baden, Tom
author_sort Zhou, Mingyi
collection PubMed
description In vertebrate vision, the tetrachromatic larval zebrafish permits non-invasive monitoring and manipulating of neural activity across the nervous system in vivo during ongoing behavior. However, despite a perhaps unparalleled understanding of links between zebrafish brain circuits and visual behaviors, comparatively little is known about what their eyes send to the brain via retinal ganglion cells (RGCs). Major gaps in knowledge include any information on spectral coding and information on potentially critical variations in RGC properties across the retinal surface corresponding with asymmetries in the statistics of natural visual space and behavioral demands. Here, we use in vivo two-photon imaging during hyperspectral visual stimulation as well as photolabeling of RGCs to provide a functional and anatomical census of RGCs in larval zebrafish. We find that RGCs’ functional and structural properties differ across the eye and include a notable population of UV-responsive On-sustained RGCs that are only found in the acute zone, likely to support visual prey capture of UV-bright zooplankton. Next, approximately half of RGCs display diverse forms of color opponency, including many that are driven by a pervasive and slow blue-Off system—far in excess of what would be required to satisfy traditional models of color vision. In addition, most information on spectral contrast was intermixed with temporal information. Taken together, our results suggest that zebrafish RGCs send a diverse and highly regionalized time-color code to the brain.
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spelling pubmed-74161132020-08-13 Zebrafish Retinal Ganglion Cells Asymmetrically Encode Spectral and Temporal Information across Visual Space Zhou, Mingyi Bear, John Roberts, Paul A. Janiak, Filip K. Semmelhack, Julie Yoshimatsu, Takeshi Baden, Tom Curr Biol Article In vertebrate vision, the tetrachromatic larval zebrafish permits non-invasive monitoring and manipulating of neural activity across the nervous system in vivo during ongoing behavior. However, despite a perhaps unparalleled understanding of links between zebrafish brain circuits and visual behaviors, comparatively little is known about what their eyes send to the brain via retinal ganglion cells (RGCs). Major gaps in knowledge include any information on spectral coding and information on potentially critical variations in RGC properties across the retinal surface corresponding with asymmetries in the statistics of natural visual space and behavioral demands. Here, we use in vivo two-photon imaging during hyperspectral visual stimulation as well as photolabeling of RGCs to provide a functional and anatomical census of RGCs in larval zebrafish. We find that RGCs’ functional and structural properties differ across the eye and include a notable population of UV-responsive On-sustained RGCs that are only found in the acute zone, likely to support visual prey capture of UV-bright zooplankton. Next, approximately half of RGCs display diverse forms of color opponency, including many that are driven by a pervasive and slow blue-Off system—far in excess of what would be required to satisfy traditional models of color vision. In addition, most information on spectral contrast was intermixed with temporal information. Taken together, our results suggest that zebrafish RGCs send a diverse and highly regionalized time-color code to the brain. Cell Press 2020-08-03 /pmc/articles/PMC7416113/ /pubmed/32531283 http://dx.doi.org/10.1016/j.cub.2020.05.055 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhou, Mingyi
Bear, John
Roberts, Paul A.
Janiak, Filip K.
Semmelhack, Julie
Yoshimatsu, Takeshi
Baden, Tom
Zebrafish Retinal Ganglion Cells Asymmetrically Encode Spectral and Temporal Information across Visual Space
title Zebrafish Retinal Ganglion Cells Asymmetrically Encode Spectral and Temporal Information across Visual Space
title_full Zebrafish Retinal Ganglion Cells Asymmetrically Encode Spectral and Temporal Information across Visual Space
title_fullStr Zebrafish Retinal Ganglion Cells Asymmetrically Encode Spectral and Temporal Information across Visual Space
title_full_unstemmed Zebrafish Retinal Ganglion Cells Asymmetrically Encode Spectral and Temporal Information across Visual Space
title_short Zebrafish Retinal Ganglion Cells Asymmetrically Encode Spectral and Temporal Information across Visual Space
title_sort zebrafish retinal ganglion cells asymmetrically encode spectral and temporal information across visual space
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416113/
https://www.ncbi.nlm.nih.gov/pubmed/32531283
http://dx.doi.org/10.1016/j.cub.2020.05.055
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