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Transcriptomic Signatures of Postnatal and Adult Intrinsically Photosensitive Ganglion Cells
Intrinsically photosensitive retinal ganglion cells (ipRGCs) are rare mammalian photoreceptors essential for non-image-forming vision functions, such as circadian photoentrainment and the pupillary light reflex. They comprise multiple subtypes distinguishable by morphology, physiology, projections,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712207/ https://www.ncbi.nlm.nih.gov/pubmed/31387875 http://dx.doi.org/10.1523/ENEURO.0022-19.2019 |
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author | Berg, Daniel J. Kartheiser, Katherine Leyrer, Megan Saali, Alexandra Berson, David M. |
author_facet | Berg, Daniel J. Kartheiser, Katherine Leyrer, Megan Saali, Alexandra Berson, David M. |
author_sort | Berg, Daniel J. |
collection | PubMed |
description | Intrinsically photosensitive retinal ganglion cells (ipRGCs) are rare mammalian photoreceptors essential for non-image-forming vision functions, such as circadian photoentrainment and the pupillary light reflex. They comprise multiple subtypes distinguishable by morphology, physiology, projections, and levels of expression of melanopsin (Opn4), their photopigment. The molecular programs that distinguish ipRGCs from other ganglion cells and ipRGC subtypes from one another remain elusive. Here, we present comprehensive gene expression profiles of early postnatal and adult mouse ipRGCs purified from two lines of reporter mice that mark different sets of ipRGC subtypes. We find dozens of novel genes highly enriched in ipRGCs. We reveal that Rasgrp1 and Tbx20 are selectively expressed in subsets of ipRGCs, though these molecularly defined groups imperfectly match established ipRGC subtypes. We demonstrate that the ipRGCs regulating circadian photoentrainment are diverse at the molecular level. Our findings reveal unexpected complexity in gene expression patterns across mammalian ipRGC subtypes. |
format | Online Article Text |
id | pubmed-6712207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-67122072019-08-28 Transcriptomic Signatures of Postnatal and Adult Intrinsically Photosensitive Ganglion Cells Berg, Daniel J. Kartheiser, Katherine Leyrer, Megan Saali, Alexandra Berson, David M. eNeuro New Research Intrinsically photosensitive retinal ganglion cells (ipRGCs) are rare mammalian photoreceptors essential for non-image-forming vision functions, such as circadian photoentrainment and the pupillary light reflex. They comprise multiple subtypes distinguishable by morphology, physiology, projections, and levels of expression of melanopsin (Opn4), their photopigment. The molecular programs that distinguish ipRGCs from other ganglion cells and ipRGC subtypes from one another remain elusive. Here, we present comprehensive gene expression profiles of early postnatal and adult mouse ipRGCs purified from two lines of reporter mice that mark different sets of ipRGC subtypes. We find dozens of novel genes highly enriched in ipRGCs. We reveal that Rasgrp1 and Tbx20 are selectively expressed in subsets of ipRGCs, though these molecularly defined groups imperfectly match established ipRGC subtypes. We demonstrate that the ipRGCs regulating circadian photoentrainment are diverse at the molecular level. Our findings reveal unexpected complexity in gene expression patterns across mammalian ipRGC subtypes. Society for Neuroscience 2019-08-23 /pmc/articles/PMC6712207/ /pubmed/31387875 http://dx.doi.org/10.1523/ENEURO.0022-19.2019 Text en Copyright © 2019 Berg et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article 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 that the original work is properly attributed. |
spellingShingle | New Research Berg, Daniel J. Kartheiser, Katherine Leyrer, Megan Saali, Alexandra Berson, David M. Transcriptomic Signatures of Postnatal and Adult Intrinsically Photosensitive Ganglion Cells |
title | Transcriptomic Signatures of Postnatal and Adult Intrinsically Photosensitive Ganglion Cells |
title_full | Transcriptomic Signatures of Postnatal and Adult Intrinsically Photosensitive Ganglion Cells |
title_fullStr | Transcriptomic Signatures of Postnatal and Adult Intrinsically Photosensitive Ganglion Cells |
title_full_unstemmed | Transcriptomic Signatures of Postnatal and Adult Intrinsically Photosensitive Ganglion Cells |
title_short | Transcriptomic Signatures of Postnatal and Adult Intrinsically Photosensitive Ganglion Cells |
title_sort | transcriptomic signatures of postnatal and adult intrinsically photosensitive ganglion cells |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712207/ https://www.ncbi.nlm.nih.gov/pubmed/31387875 http://dx.doi.org/10.1523/ENEURO.0022-19.2019 |
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