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Retinal patterns and the cellular repertoire of neuropsin (Opn5) retinal ganglion cells
Obtaining a parts list of the sensory components of the retina is vital to understand the effects of light in behavior, health, and disease. Rods, cones, and intrinsically photosensitive retinal ganglion cells (ipRGCs) are the best described photoreceptors in the mammalian retina, but recent functio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969148/ https://www.ncbi.nlm.nih.gov/pubmed/34743323 http://dx.doi.org/10.1002/cne.25272 |
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author | D'Souza, Shane P. Swygart, David I. Wienbar, Sophia R. Upton, Brian A. Zhang, Kevin X. Mackin, Robert D. Casasent, Anna K. Samuel, Melanie A. Schwartz, Gregory W. Lang, Richard A. |
author_facet | D'Souza, Shane P. Swygart, David I. Wienbar, Sophia R. Upton, Brian A. Zhang, Kevin X. Mackin, Robert D. Casasent, Anna K. Samuel, Melanie A. Schwartz, Gregory W. Lang, Richard A. |
author_sort | D'Souza, Shane P. |
collection | PubMed |
description | Obtaining a parts list of the sensory components of the retina is vital to understand the effects of light in behavior, health, and disease. Rods, cones, and intrinsically photosensitive retinal ganglion cells (ipRGCs) are the best described photoreceptors in the mammalian retina, but recent functional roles have been proposed for retinal neuropsin (Opn5)—an atypical opsin. However, little is known about the pattern of Opn5 expression in the retina. Using cre (Opn5(cre) ) and cre‐dependent reporters, we uncover patterns of Opn5 expression and find that Opn5 is restricted to retinal ganglion cells (RGCs). Opn5‐RGCs are nonhomogenously distributed through the retina, with greater densities of cells located in the dorsotemporal quadrant. In addition to the local topology of these cells, using cre‐dependent AAV viral tracing, we surveyed their central targets and found that they are biased towards image‐forming and image‐stabilizing regions. Finally, molecular and electrophysiological profiling reveal that Opn5‐RGCs comprise previously defined RGC types that respond optimally to edges and object‐motion (F‐mini‐ONs, HD2, HD1, LEDs, ooDSRGCs, etc.). Together, these data describe the second collection of RGCs that express atypical opsins in the mouse, and expand the roles of image‐forming cells in retinal physiology and function. |
format | Online Article Text |
id | pubmed-8969148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89691482022-10-14 Retinal patterns and the cellular repertoire of neuropsin (Opn5) retinal ganglion cells D'Souza, Shane P. Swygart, David I. Wienbar, Sophia R. Upton, Brian A. Zhang, Kevin X. Mackin, Robert D. Casasent, Anna K. Samuel, Melanie A. Schwartz, Gregory W. Lang, Richard A. J Comp Neurol Research Articles Obtaining a parts list of the sensory components of the retina is vital to understand the effects of light in behavior, health, and disease. Rods, cones, and intrinsically photosensitive retinal ganglion cells (ipRGCs) are the best described photoreceptors in the mammalian retina, but recent functional roles have been proposed for retinal neuropsin (Opn5)—an atypical opsin. However, little is known about the pattern of Opn5 expression in the retina. Using cre (Opn5(cre) ) and cre‐dependent reporters, we uncover patterns of Opn5 expression and find that Opn5 is restricted to retinal ganglion cells (RGCs). Opn5‐RGCs are nonhomogenously distributed through the retina, with greater densities of cells located in the dorsotemporal quadrant. In addition to the local topology of these cells, using cre‐dependent AAV viral tracing, we surveyed their central targets and found that they are biased towards image‐forming and image‐stabilizing regions. Finally, molecular and electrophysiological profiling reveal that Opn5‐RGCs comprise previously defined RGC types that respond optimally to edges and object‐motion (F‐mini‐ONs, HD2, HD1, LEDs, ooDSRGCs, etc.). Together, these data describe the second collection of RGCs that express atypical opsins in the mouse, and expand the roles of image‐forming cells in retinal physiology and function. John Wiley and Sons Inc. 2021-12-15 2022-06 /pmc/articles/PMC8969148/ /pubmed/34743323 http://dx.doi.org/10.1002/cne.25272 Text en © 2021 The Authors. The Journal of Comparative Neurology published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles D'Souza, Shane P. Swygart, David I. Wienbar, Sophia R. Upton, Brian A. Zhang, Kevin X. Mackin, Robert D. Casasent, Anna K. Samuel, Melanie A. Schwartz, Gregory W. Lang, Richard A. Retinal patterns and the cellular repertoire of neuropsin (Opn5) retinal ganglion cells |
title | Retinal patterns and the cellular repertoire of neuropsin (Opn5) retinal ganglion cells |
title_full | Retinal patterns and the cellular repertoire of neuropsin (Opn5) retinal ganglion cells |
title_fullStr | Retinal patterns and the cellular repertoire of neuropsin (Opn5) retinal ganglion cells |
title_full_unstemmed | Retinal patterns and the cellular repertoire of neuropsin (Opn5) retinal ganglion cells |
title_short | Retinal patterns and the cellular repertoire of neuropsin (Opn5) retinal ganglion cells |
title_sort | retinal patterns and the cellular repertoire of neuropsin (opn5) retinal ganglion cells |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969148/ https://www.ncbi.nlm.nih.gov/pubmed/34743323 http://dx.doi.org/10.1002/cne.25272 |
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