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Synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina

Ganglion cells are the projection neurons of the retina. Intrinsically photosensitive retinal ganglion cells (ipRGCs) express the photopigment melanopsin and also receive input from rods and cones via bipolar cells and amacrine cells. In primates, multiple types of ipRGCs have been identified. The i...

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Autores principales: Bordt, Andrea S., Patterson, Sara S., Kuchenbecker, James A., Mazzaferri, Marcus A., Yearick, Joel N., Yang, Emma R., Ogilvie, Judith Mosinger, Neitz, Jay, Marshak, David W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9452553/
https://www.ncbi.nlm.nih.gov/pubmed/36071126
http://dx.doi.org/10.1038/s41598-022-19324-z
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author Bordt, Andrea S.
Patterson, Sara S.
Kuchenbecker, James A.
Mazzaferri, Marcus A.
Yearick, Joel N.
Yang, Emma R.
Ogilvie, Judith Mosinger
Neitz, Jay
Marshak, David W.
author_facet Bordt, Andrea S.
Patterson, Sara S.
Kuchenbecker, James A.
Mazzaferri, Marcus A.
Yearick, Joel N.
Yang, Emma R.
Ogilvie, Judith Mosinger
Neitz, Jay
Marshak, David W.
author_sort Bordt, Andrea S.
collection PubMed
description Ganglion cells are the projection neurons of the retina. Intrinsically photosensitive retinal ganglion cells (ipRGCs) express the photopigment melanopsin and also receive input from rods and cones via bipolar cells and amacrine cells. In primates, multiple types of ipRGCs have been identified. The ipRGCs with somas in the ganglion cell layer have been studied extensively, but less is known about those with somas in the inner nuclear layer, the “displaced” cells. To investigate their synaptic inputs, three sets of horizontal, ultrathin sections through central macaque retina were collected using serial block-face scanning electron microscopy. One displaced ipRGC received nearly all of its excitatory inputs from ON bipolar cells and would therefore be expected to have ON responses to light. In each of the three volumes, there was also at least one cell that had a large soma in the inner nuclear layer, varicose axons and dendrites with a large diameter that formed large, extremely sparse arbor in the outermost stratum of the inner plexiform layer. They were identified as the displaced M1 type of ipRGCs based on this morphology and on the high density of granules in their somas. They received extensive input from amacrine cells, including the dopaminergic type. The vast majority of their excitatory inputs were from OFF bipolar cells, including two subtypes with extensive input from the primary rod pathway. They would be expected to have OFF responses to light stimuli below the threshold for melanopsin or soon after the offset of a light stimulus.
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spelling pubmed-94525532022-09-09 Synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina Bordt, Andrea S. Patterson, Sara S. Kuchenbecker, James A. Mazzaferri, Marcus A. Yearick, Joel N. Yang, Emma R. Ogilvie, Judith Mosinger Neitz, Jay Marshak, David W. Sci Rep Article Ganglion cells are the projection neurons of the retina. Intrinsically photosensitive retinal ganglion cells (ipRGCs) express the photopigment melanopsin and also receive input from rods and cones via bipolar cells and amacrine cells. In primates, multiple types of ipRGCs have been identified. The ipRGCs with somas in the ganglion cell layer have been studied extensively, but less is known about those with somas in the inner nuclear layer, the “displaced” cells. To investigate their synaptic inputs, three sets of horizontal, ultrathin sections through central macaque retina were collected using serial block-face scanning electron microscopy. One displaced ipRGC received nearly all of its excitatory inputs from ON bipolar cells and would therefore be expected to have ON responses to light. In each of the three volumes, there was also at least one cell that had a large soma in the inner nuclear layer, varicose axons and dendrites with a large diameter that formed large, extremely sparse arbor in the outermost stratum of the inner plexiform layer. They were identified as the displaced M1 type of ipRGCs based on this morphology and on the high density of granules in their somas. They received extensive input from amacrine cells, including the dopaminergic type. The vast majority of their excitatory inputs were from OFF bipolar cells, including two subtypes with extensive input from the primary rod pathway. They would be expected to have OFF responses to light stimuli below the threshold for melanopsin or soon after the offset of a light stimulus. Nature Publishing Group UK 2022-09-07 /pmc/articles/PMC9452553/ /pubmed/36071126 http://dx.doi.org/10.1038/s41598-022-19324-z Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bordt, Andrea S.
Patterson, Sara S.
Kuchenbecker, James A.
Mazzaferri, Marcus A.
Yearick, Joel N.
Yang, Emma R.
Ogilvie, Judith Mosinger
Neitz, Jay
Marshak, David W.
Synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina
title Synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina
title_full Synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina
title_fullStr Synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina
title_full_unstemmed Synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina
title_short Synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina
title_sort synaptic inputs to displaced intrinsically-photosensitive ganglion cells in macaque retina
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9452553/
https://www.ncbi.nlm.nih.gov/pubmed/36071126
http://dx.doi.org/10.1038/s41598-022-19324-z
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