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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,...

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Autores principales: Berg, Daniel J., Kartheiser, Katherine, Leyrer, Megan, Saali, Alexandra, Berson, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2019
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.
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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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