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Strategic Positioning of Connexin36 Gap Junctions Across Human Retinal Ganglion Cell Dendritic Arbors

Connexin36 (Cx36) subunits form gap junctions (GJ) between neurons throughout the central nervous system. Such GJs of the mammalian retina serve the transmission, averaging and correlation of signals prior to conveying visual information to the brain. Retinal GJs have been exhaustively studied in va...

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Autores principales: Kántor, Orsolya, Szarka, Gergely, Benkő, Zsigmond, Somogyvári, Zoltán, Pálfi, Emese, Baksa, Gábor, Rácz, Gergely, Nitschke, Roland, Debertin, Gábor, Völgyi, Béla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262005/
https://www.ncbi.nlm.nih.gov/pubmed/30524239
http://dx.doi.org/10.3389/fncel.2018.00409
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author Kántor, Orsolya
Szarka, Gergely
Benkő, Zsigmond
Somogyvári, Zoltán
Pálfi, Emese
Baksa, Gábor
Rácz, Gergely
Nitschke, Roland
Debertin, Gábor
Völgyi, Béla
author_facet Kántor, Orsolya
Szarka, Gergely
Benkő, Zsigmond
Somogyvári, Zoltán
Pálfi, Emese
Baksa, Gábor
Rácz, Gergely
Nitschke, Roland
Debertin, Gábor
Völgyi, Béla
author_sort Kántor, Orsolya
collection PubMed
description Connexin36 (Cx36) subunits form gap junctions (GJ) between neurons throughout the central nervous system. Such GJs of the mammalian retina serve the transmission, averaging and correlation of signals prior to conveying visual information to the brain. Retinal GJs have been exhaustively studied in various animal species, however, there is still a perplexing paucity of information regarding the presence and function of human retinal GJs. Particularly little is known about GJ formation of human retinal ganglion cells (hRGCs) due to the limited number of suitable experimental approaches. Compared to the neuronal coupling studies in animal models, where GJ permeable tracer injection is the gold standard method, the post-mortem nature of scarcely available human retinal samples leaves immunohistochemistry as a sole approach to obtain information on hRGC GJs. In this study Lucifer Yellow (LY) dye injections and Cx36 immunohistochemistry were performed in fixed short-post-mortem samples to stain hRGCs with complete dendritic arbors and locate dendritic Cx36 GJs. Subsequent neuronal reconstructions and morphometric analyses revealed that Cx36 plaques had a clear tendency to form clusters and particularly favored terminal dendritic segments.
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spelling pubmed-62620052018-12-06 Strategic Positioning of Connexin36 Gap Junctions Across Human Retinal Ganglion Cell Dendritic Arbors Kántor, Orsolya Szarka, Gergely Benkő, Zsigmond Somogyvári, Zoltán Pálfi, Emese Baksa, Gábor Rácz, Gergely Nitschke, Roland Debertin, Gábor Völgyi, Béla Front Cell Neurosci Neuroscience Connexin36 (Cx36) subunits form gap junctions (GJ) between neurons throughout the central nervous system. Such GJs of the mammalian retina serve the transmission, averaging and correlation of signals prior to conveying visual information to the brain. Retinal GJs have been exhaustively studied in various animal species, however, there is still a perplexing paucity of information regarding the presence and function of human retinal GJs. Particularly little is known about GJ formation of human retinal ganglion cells (hRGCs) due to the limited number of suitable experimental approaches. Compared to the neuronal coupling studies in animal models, where GJ permeable tracer injection is the gold standard method, the post-mortem nature of scarcely available human retinal samples leaves immunohistochemistry as a sole approach to obtain information on hRGC GJs. In this study Lucifer Yellow (LY) dye injections and Cx36 immunohistochemistry were performed in fixed short-post-mortem samples to stain hRGCs with complete dendritic arbors and locate dendritic Cx36 GJs. Subsequent neuronal reconstructions and morphometric analyses revealed that Cx36 plaques had a clear tendency to form clusters and particularly favored terminal dendritic segments. Frontiers Media S.A. 2018-11-22 /pmc/articles/PMC6262005/ /pubmed/30524239 http://dx.doi.org/10.3389/fncel.2018.00409 Text en Copyright © 2018 Kántor, Szarka, Benkő, Somogyvári, Pálfi, Baksa, Rácz, Nitschke, Debertin and Völgyi. http://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 Neuroscience
Kántor, Orsolya
Szarka, Gergely
Benkő, Zsigmond
Somogyvári, Zoltán
Pálfi, Emese
Baksa, Gábor
Rácz, Gergely
Nitschke, Roland
Debertin, Gábor
Völgyi, Béla
Strategic Positioning of Connexin36 Gap Junctions Across Human Retinal Ganglion Cell Dendritic Arbors
title Strategic Positioning of Connexin36 Gap Junctions Across Human Retinal Ganglion Cell Dendritic Arbors
title_full Strategic Positioning of Connexin36 Gap Junctions Across Human Retinal Ganglion Cell Dendritic Arbors
title_fullStr Strategic Positioning of Connexin36 Gap Junctions Across Human Retinal Ganglion Cell Dendritic Arbors
title_full_unstemmed Strategic Positioning of Connexin36 Gap Junctions Across Human Retinal Ganglion Cell Dendritic Arbors
title_short Strategic Positioning of Connexin36 Gap Junctions Across Human Retinal Ganglion Cell Dendritic Arbors
title_sort strategic positioning of connexin36 gap junctions across human retinal ganglion cell dendritic arbors
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262005/
https://www.ncbi.nlm.nih.gov/pubmed/30524239
http://dx.doi.org/10.3389/fncel.2018.00409
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