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FLRT3 Marks Direction-Selective Retinal Ganglion Cells That Project to the Medial Terminal Nucleus

The mammalian retina extracts a multitude of diverse features from the visual scene such as color, contrast, and direction of motion. These features are transmitted separately to the brain by more than 40 different retinal ganglion cell (RGC) subtypes. However, so far only a few genetic markers exis...

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Autores principales: Ruff, Tobias, Peters, Christian, Matsumoto, Akihiro, Ihle, Stephan J., Morales, Pilar Alcalá, Gaitanos, Louise, Yonehara, Keisuke, del Toro, Daniel, Klein, Rüdiger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8696037/
https://www.ncbi.nlm.nih.gov/pubmed/34955746
http://dx.doi.org/10.3389/fnmol.2021.790466
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author Ruff, Tobias
Peters, Christian
Matsumoto, Akihiro
Ihle, Stephan J.
Morales, Pilar Alcalá
Gaitanos, Louise
Yonehara, Keisuke
del Toro, Daniel
Klein, Rüdiger
author_facet Ruff, Tobias
Peters, Christian
Matsumoto, Akihiro
Ihle, Stephan J.
Morales, Pilar Alcalá
Gaitanos, Louise
Yonehara, Keisuke
del Toro, Daniel
Klein, Rüdiger
author_sort Ruff, Tobias
collection PubMed
description The mammalian retina extracts a multitude of diverse features from the visual scene such as color, contrast, and direction of motion. These features are transmitted separately to the brain by more than 40 different retinal ganglion cell (RGC) subtypes. However, so far only a few genetic markers exist to fully characterize the different RGC subtypes. Here, we present a novel genetic Flrt3-CreERT2 knock-in mouse that labels a small subpopulation of RGCs. Using single-cell injection of fluorescent dyes in Flrt3 positive RGCs, we distinguished four morphological RGC subtypes. Anterograde tracings using a fluorescent Cre-dependent Adeno-associated virus (AAV) revealed that a subgroup of Flrt3 positive RGCs specifically project to the medial terminal nucleus (MTN), which is part of the accessory optic system (AOS) and is essential in driving reflex eye movements for retinal image stabilization. Functional characterization using ex vivo patch-clamp recordings showed that the MTN-projecting Flrt3 RGCs preferentially respond to downward motion in an ON-fashion. These neurons distribute in a regular pattern and most of them are bistratified at the level of the ON and OFF bands of cholinergic starburst amacrine cells where they express the known ON-OFF direction-selective RGC marker CART. Together, our results indicate that MTN-projecting Flrt3 RGCs represent a new functionally homogeneous AOS projecting direction-selective RGC subpopulation.
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spelling pubmed-86960372021-12-24 FLRT3 Marks Direction-Selective Retinal Ganglion Cells That Project to the Medial Terminal Nucleus Ruff, Tobias Peters, Christian Matsumoto, Akihiro Ihle, Stephan J. Morales, Pilar Alcalá Gaitanos, Louise Yonehara, Keisuke del Toro, Daniel Klein, Rüdiger Front Mol Neurosci Molecular Neuroscience The mammalian retina extracts a multitude of diverse features from the visual scene such as color, contrast, and direction of motion. These features are transmitted separately to the brain by more than 40 different retinal ganglion cell (RGC) subtypes. However, so far only a few genetic markers exist to fully characterize the different RGC subtypes. Here, we present a novel genetic Flrt3-CreERT2 knock-in mouse that labels a small subpopulation of RGCs. Using single-cell injection of fluorescent dyes in Flrt3 positive RGCs, we distinguished four morphological RGC subtypes. Anterograde tracings using a fluorescent Cre-dependent Adeno-associated virus (AAV) revealed that a subgroup of Flrt3 positive RGCs specifically project to the medial terminal nucleus (MTN), which is part of the accessory optic system (AOS) and is essential in driving reflex eye movements for retinal image stabilization. Functional characterization using ex vivo patch-clamp recordings showed that the MTN-projecting Flrt3 RGCs preferentially respond to downward motion in an ON-fashion. These neurons distribute in a regular pattern and most of them are bistratified at the level of the ON and OFF bands of cholinergic starburst amacrine cells where they express the known ON-OFF direction-selective RGC marker CART. Together, our results indicate that MTN-projecting Flrt3 RGCs represent a new functionally homogeneous AOS projecting direction-selective RGC subpopulation. Frontiers Media S.A. 2021-12-09 /pmc/articles/PMC8696037/ /pubmed/34955746 http://dx.doi.org/10.3389/fnmol.2021.790466 Text en Copyright © 2021 Ruff, Peters, Matsumoto, Ihle, Morales, Gaitanos, Yonehara, del Toro and Klein. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Neuroscience
Ruff, Tobias
Peters, Christian
Matsumoto, Akihiro
Ihle, Stephan J.
Morales, Pilar Alcalá
Gaitanos, Louise
Yonehara, Keisuke
del Toro, Daniel
Klein, Rüdiger
FLRT3 Marks Direction-Selective Retinal Ganglion Cells That Project to the Medial Terminal Nucleus
title FLRT3 Marks Direction-Selective Retinal Ganglion Cells That Project to the Medial Terminal Nucleus
title_full FLRT3 Marks Direction-Selective Retinal Ganglion Cells That Project to the Medial Terminal Nucleus
title_fullStr FLRT3 Marks Direction-Selective Retinal Ganglion Cells That Project to the Medial Terminal Nucleus
title_full_unstemmed FLRT3 Marks Direction-Selective Retinal Ganglion Cells That Project to the Medial Terminal Nucleus
title_short FLRT3 Marks Direction-Selective Retinal Ganglion Cells That Project to the Medial Terminal Nucleus
title_sort flrt3 marks direction-selective retinal ganglion cells that project to the medial terminal nucleus
topic Molecular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8696037/
https://www.ncbi.nlm.nih.gov/pubmed/34955746
http://dx.doi.org/10.3389/fnmol.2021.790466
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