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Plasticity of Scarpa’s Ganglion Neurons as a Possible Basis for Functional Restoration within Vestibular Endorgans
In a previous study, we observed spontaneous restoration of vestibular function in young adult rodents following excitotoxic injury of the neuronal connections within vestibular endorgans. The functional restoration was supported by a repair of synaptic contacts between hair cells and primary vestib...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368229/ https://www.ncbi.nlm.nih.gov/pubmed/22685444 http://dx.doi.org/10.3389/fneur.2012.00091 |
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author | Travo, Cécile Gaboyard-Niay, Sophie Chabbert, Christian |
author_facet | Travo, Cécile Gaboyard-Niay, Sophie Chabbert, Christian |
author_sort | Travo, Cécile |
collection | PubMed |
description | In a previous study, we observed spontaneous restoration of vestibular function in young adult rodents following excitotoxic injury of the neuronal connections within vestibular endorgans. The functional restoration was supported by a repair of synaptic contacts between hair cells and primary vestibular neurons. This process was observed in 2/3 of the animals studied and occurred within 5 days following the synaptic damage. To assess whether repair capacity is a fundamental trait of vestibular endorgans and to decipher the cellular mechanisms supporting such a repair process, we studied the neuronal regeneration and synaptogenesis in co-cultures of vestibular epithelia and Scarpa’s ganglion from young and adult rodents. We demonstrate that, under specific culture conditions, primary vestibular neurons from young mice or rats exhibit robust ability to regenerate nervous processes. When co-cultured with vestibular epithelia, primary vestibular neurons were able to establish de novo contacts with hair cells. Under the present paradigm, these contacts displayed morphological features of immature synaptic contacts. Preliminary observations using co-cultures of adult rodents suggest that this reparative capacity remained in older mice although to a lesser extent. Identifying the basic mechanisms underlying the repair process may provide a basis for novel therapeutic strategies to restore mature and functional vestibular synaptic contacts following damage or loss. |
format | Online Article Text |
id | pubmed-3368229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33682292012-06-08 Plasticity of Scarpa’s Ganglion Neurons as a Possible Basis for Functional Restoration within Vestibular Endorgans Travo, Cécile Gaboyard-Niay, Sophie Chabbert, Christian Front Neurol Neuroscience In a previous study, we observed spontaneous restoration of vestibular function in young adult rodents following excitotoxic injury of the neuronal connections within vestibular endorgans. The functional restoration was supported by a repair of synaptic contacts between hair cells and primary vestibular neurons. This process was observed in 2/3 of the animals studied and occurred within 5 days following the synaptic damage. To assess whether repair capacity is a fundamental trait of vestibular endorgans and to decipher the cellular mechanisms supporting such a repair process, we studied the neuronal regeneration and synaptogenesis in co-cultures of vestibular epithelia and Scarpa’s ganglion from young and adult rodents. We demonstrate that, under specific culture conditions, primary vestibular neurons from young mice or rats exhibit robust ability to regenerate nervous processes. When co-cultured with vestibular epithelia, primary vestibular neurons were able to establish de novo contacts with hair cells. Under the present paradigm, these contacts displayed morphological features of immature synaptic contacts. Preliminary observations using co-cultures of adult rodents suggest that this reparative capacity remained in older mice although to a lesser extent. Identifying the basic mechanisms underlying the repair process may provide a basis for novel therapeutic strategies to restore mature and functional vestibular synaptic contacts following damage or loss. Frontiers Research Foundation 2012-06-06 /pmc/articles/PMC3368229/ /pubmed/22685444 http://dx.doi.org/10.3389/fneur.2012.00091 Text en Copyright © 2012 Travo, Gaboyard-Niay and Chabbert. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Neuroscience Travo, Cécile Gaboyard-Niay, Sophie Chabbert, Christian Plasticity of Scarpa’s Ganglion Neurons as a Possible Basis for Functional Restoration within Vestibular Endorgans |
title | Plasticity of Scarpa’s Ganglion Neurons as a Possible Basis for Functional Restoration within Vestibular Endorgans |
title_full | Plasticity of Scarpa’s Ganglion Neurons as a Possible Basis for Functional Restoration within Vestibular Endorgans |
title_fullStr | Plasticity of Scarpa’s Ganglion Neurons as a Possible Basis for Functional Restoration within Vestibular Endorgans |
title_full_unstemmed | Plasticity of Scarpa’s Ganglion Neurons as a Possible Basis for Functional Restoration within Vestibular Endorgans |
title_short | Plasticity of Scarpa’s Ganglion Neurons as a Possible Basis for Functional Restoration within Vestibular Endorgans |
title_sort | plasticity of scarpa’s ganglion neurons as a possible basis for functional restoration within vestibular endorgans |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368229/ https://www.ncbi.nlm.nih.gov/pubmed/22685444 http://dx.doi.org/10.3389/fneur.2012.00091 |
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