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A melanopsin ganglion cell subtype forms a dorsal retinal mosaic projecting to the supraoptic nucleus
Visual input to the hypothalamus from intrinsically photosensitive retinal ganglion cells (ipRGCs) influences several functions including circadian entrainment, body temperature, and sleep. ipRGCs also project to nuclei such as the supraoptic nucleus (SON), which is involved in systemic fluid homeos...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023714/ https://www.ncbi.nlm.nih.gov/pubmed/36932080 http://dx.doi.org/10.1038/s41467-023-36955-6 |
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author | Berry, Michael H. Moldavan, Michael Garrett, Tavita Meadows, Marc Cravetchi, Olga White, Elizabeth Leffler, Joseph von Gersdorff, Henrique Wright, Kevin M. Allen, Charles N. Sivyer, Benjamin |
author_facet | Berry, Michael H. Moldavan, Michael Garrett, Tavita Meadows, Marc Cravetchi, Olga White, Elizabeth Leffler, Joseph von Gersdorff, Henrique Wright, Kevin M. Allen, Charles N. Sivyer, Benjamin |
author_sort | Berry, Michael H. |
collection | PubMed |
description | Visual input to the hypothalamus from intrinsically photosensitive retinal ganglion cells (ipRGCs) influences several functions including circadian entrainment, body temperature, and sleep. ipRGCs also project to nuclei such as the supraoptic nucleus (SON), which is involved in systemic fluid homeostasis, maternal behavior, social behaviors, and appetite. However, little is known about the SON-projecting ipRGCs or their relationship to well-characterized ipRGC subtypes. Using a GlyT2(Cre) mouse line, we show a subtype of ipRGCs restricted to the dorsal retina that selectively projects to the SON. These ipRGCs tile a dorsal region of the retina, forming a substrate for encoding ground luminance. Optogenetic activation of their axons demonstrates they release the neurotransmitter glutamate in multiple regions, including the suprachiasmatic nucleus (SCN) and SON. Our results challenge the idea that ipRGC dendrites overlap to optimize photon capture and suggests non-image forming vision operates to sample local regions of the visual field to influence diverse behaviors. |
format | Online Article Text |
id | pubmed-10023714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100237142023-03-19 A melanopsin ganglion cell subtype forms a dorsal retinal mosaic projecting to the supraoptic nucleus Berry, Michael H. Moldavan, Michael Garrett, Tavita Meadows, Marc Cravetchi, Olga White, Elizabeth Leffler, Joseph von Gersdorff, Henrique Wright, Kevin M. Allen, Charles N. Sivyer, Benjamin Nat Commun Article Visual input to the hypothalamus from intrinsically photosensitive retinal ganglion cells (ipRGCs) influences several functions including circadian entrainment, body temperature, and sleep. ipRGCs also project to nuclei such as the supraoptic nucleus (SON), which is involved in systemic fluid homeostasis, maternal behavior, social behaviors, and appetite. However, little is known about the SON-projecting ipRGCs or their relationship to well-characterized ipRGC subtypes. Using a GlyT2(Cre) mouse line, we show a subtype of ipRGCs restricted to the dorsal retina that selectively projects to the SON. These ipRGCs tile a dorsal region of the retina, forming a substrate for encoding ground luminance. Optogenetic activation of their axons demonstrates they release the neurotransmitter glutamate in multiple regions, including the suprachiasmatic nucleus (SCN) and SON. Our results challenge the idea that ipRGC dendrites overlap to optimize photon capture and suggests non-image forming vision operates to sample local regions of the visual field to influence diverse behaviors. Nature Publishing Group UK 2023-03-17 /pmc/articles/PMC10023714/ /pubmed/36932080 http://dx.doi.org/10.1038/s41467-023-36955-6 Text en © The Author(s) 2023 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Berry, Michael H. Moldavan, Michael Garrett, Tavita Meadows, Marc Cravetchi, Olga White, Elizabeth Leffler, Joseph von Gersdorff, Henrique Wright, Kevin M. Allen, Charles N. Sivyer, Benjamin A melanopsin ganglion cell subtype forms a dorsal retinal mosaic projecting to the supraoptic nucleus |
title | A melanopsin ganglion cell subtype forms a dorsal retinal mosaic projecting to the supraoptic nucleus |
title_full | A melanopsin ganglion cell subtype forms a dorsal retinal mosaic projecting to the supraoptic nucleus |
title_fullStr | A melanopsin ganglion cell subtype forms a dorsal retinal mosaic projecting to the supraoptic nucleus |
title_full_unstemmed | A melanopsin ganglion cell subtype forms a dorsal retinal mosaic projecting to the supraoptic nucleus |
title_short | A melanopsin ganglion cell subtype forms a dorsal retinal mosaic projecting to the supraoptic nucleus |
title_sort | melanopsin ganglion cell subtype forms a dorsal retinal mosaic projecting to the supraoptic nucleus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023714/ https://www.ncbi.nlm.nih.gov/pubmed/36932080 http://dx.doi.org/10.1038/s41467-023-36955-6 |
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