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An ON-type direction-selective ganglion cell in primate retina
To maintain a stable and clear image of the world, our eyes reflexively follow the direction in which a visual scene is moving. Such gaze-stabilization mechanisms reduce image blur as we move in the environment. In non-primate mammals, this behaviour is initiated by retinal output neurons called ON-...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632142/ https://www.ncbi.nlm.nih.gov/pubmed/37880369 http://dx.doi.org/10.1038/s41586-023-06659-4 |
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author | Wang, Anna Y. M. Kulkarni, Manoj M. McLaughlin, Amanda J. Gayet, Jacqueline Smith, Benjamin E. Hauptschein, Max McHugh, Cyrus F. Yao, Yvette Y. Puthussery, Teresa |
author_facet | Wang, Anna Y. M. Kulkarni, Manoj M. McLaughlin, Amanda J. Gayet, Jacqueline Smith, Benjamin E. Hauptschein, Max McHugh, Cyrus F. Yao, Yvette Y. Puthussery, Teresa |
author_sort | Wang, Anna Y. M. |
collection | PubMed |
description | To maintain a stable and clear image of the world, our eyes reflexively follow the direction in which a visual scene is moving. Such gaze-stabilization mechanisms reduce image blur as we move in the environment. In non-primate mammals, this behaviour is initiated by retinal output neurons called ON-type direction-selective ganglion cells (ON-DSGCs), which detect the direction of image motion and transmit signals to brainstem nuclei that drive compensatory eye movements(1). However, ON-DSGCs have not yet been identified in the retina of primates, raising the possibility that this reflex is mediated by cortical visual areas. Here we mined single-cell RNA transcriptomic data from primate retina to identify a candidate ON-DSGC. We then combined two-photon calcium imaging, molecular identification and morphological analysis to reveal a population of ON-DSGCs in the macaque retina. The morphology, molecular signature and GABA (γ-aminobutyric acid)-dependent mechanisms that underlie direction selectivity in primate ON-DSGCs are highly conserved with those in other mammals. We further identify a candidate ON-DSGC in human retina. The presence of ON-DSGCs in primates highlights the need to examine the contribution of subcortical retinal mechanisms to normal and aberrant gaze stabilization in the developing and mature visual system. |
format | Online Article Text |
id | pubmed-10632142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106321422023-11-10 An ON-type direction-selective ganglion cell in primate retina Wang, Anna Y. M. Kulkarni, Manoj M. McLaughlin, Amanda J. Gayet, Jacqueline Smith, Benjamin E. Hauptschein, Max McHugh, Cyrus F. Yao, Yvette Y. Puthussery, Teresa Nature Article To maintain a stable and clear image of the world, our eyes reflexively follow the direction in which a visual scene is moving. Such gaze-stabilization mechanisms reduce image blur as we move in the environment. In non-primate mammals, this behaviour is initiated by retinal output neurons called ON-type direction-selective ganglion cells (ON-DSGCs), which detect the direction of image motion and transmit signals to brainstem nuclei that drive compensatory eye movements(1). However, ON-DSGCs have not yet been identified in the retina of primates, raising the possibility that this reflex is mediated by cortical visual areas. Here we mined single-cell RNA transcriptomic data from primate retina to identify a candidate ON-DSGC. We then combined two-photon calcium imaging, molecular identification and morphological analysis to reveal a population of ON-DSGCs in the macaque retina. The morphology, molecular signature and GABA (γ-aminobutyric acid)-dependent mechanisms that underlie direction selectivity in primate ON-DSGCs are highly conserved with those in other mammals. We further identify a candidate ON-DSGC in human retina. The presence of ON-DSGCs in primates highlights the need to examine the contribution of subcortical retinal mechanisms to normal and aberrant gaze stabilization in the developing and mature visual system. Nature Publishing Group UK 2023-10-25 2023 /pmc/articles/PMC10632142/ /pubmed/37880369 http://dx.doi.org/10.1038/s41586-023-06659-4 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 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 Wang, Anna Y. M. Kulkarni, Manoj M. McLaughlin, Amanda J. Gayet, Jacqueline Smith, Benjamin E. Hauptschein, Max McHugh, Cyrus F. Yao, Yvette Y. Puthussery, Teresa An ON-type direction-selective ganglion cell in primate retina |
title | An ON-type direction-selective ganglion cell in primate retina |
title_full | An ON-type direction-selective ganglion cell in primate retina |
title_fullStr | An ON-type direction-selective ganglion cell in primate retina |
title_full_unstemmed | An ON-type direction-selective ganglion cell in primate retina |
title_short | An ON-type direction-selective ganglion cell in primate retina |
title_sort | on-type direction-selective ganglion cell in primate retina |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632142/ https://www.ncbi.nlm.nih.gov/pubmed/37880369 http://dx.doi.org/10.1038/s41586-023-06659-4 |
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