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Spiral ganglion cells and macrophages initiate neuro-inflammation and scarring following cochlear implantation
Conservation of a patient's residual hearing and prevention of fibrous tissue/new bone formation around an electrode array are some of the major challenges in cochlear implant (CI) surgery. Although it is well-known that fibrotic tissue formation around the electrode array can interfere with he...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532929/ https://www.ncbi.nlm.nih.gov/pubmed/26321909 http://dx.doi.org/10.3389/fncel.2015.00303 |
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author | Bas, Esperanza Goncalves, Stefania Adams, Michelle Dinh, Christine T. Bas, Jose M. Van De Water, Thomas R. Eshraghi, Adrien A. |
author_facet | Bas, Esperanza Goncalves, Stefania Adams, Michelle Dinh, Christine T. Bas, Jose M. Van De Water, Thomas R. Eshraghi, Adrien A. |
author_sort | Bas, Esperanza |
collection | PubMed |
description | Conservation of a patient's residual hearing and prevention of fibrous tissue/new bone formation around an electrode array are some of the major challenges in cochlear implant (CI) surgery. Although it is well-known that fibrotic tissue formation around the electrode array can interfere with hearing performance in implanted patients, and that associated intracochlear inflammation can initiate loss of residual hearing, little is known about the molecular and cellular mechanisms that promote this response in the cochlea. In vitro studies in neonatal rats and in vivo studies in adult mice were performed to gain insight into the pro-inflammatory, proliferative, and remodeling phases of pathological wound healing that occur in the cochlea following an electrode analog insertion. Resident Schwann cells (SC), macrophages, and fibroblasts had a prominent role in the inflammatory process in the cochlea. Leukocytes were recruited to the cochlea following insertion of a nylon filament in adult mice, where contributed to the inflammatory response. The reparative stages in wound healing are characterized by persistent neuro-inflammation of spiral ganglion neurons (SGN) and expression of regenerative monocytes/macrophages in the cochlea. Accordingly, genes involved in extracellular matrix (ECM) deposition and remodeling were up-regulated in implanted cochleae. Maturation of scar tissue occurs in the remodeling phase of wound healing in the cochlea. Similar to other damaged peripheral nerves, M2 macrophages and de-differentiated SC were observed in damaged cochleae and may play a role in cell survival and axonal regeneration. In conclusion, the insertion of an electrode analog into the cochlea is associated with robust early and chronic inflammatory responses characterized by recruitment of leukocytes and expression of pro-inflammatory cytokines that promote intracochlear fibrosis and loss of the auditory hair cells (HC) and SGN important for hearing after CI surgery. |
format | Online Article Text |
id | pubmed-4532929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45329292015-08-28 Spiral ganglion cells and macrophages initiate neuro-inflammation and scarring following cochlear implantation Bas, Esperanza Goncalves, Stefania Adams, Michelle Dinh, Christine T. Bas, Jose M. Van De Water, Thomas R. Eshraghi, Adrien A. Front Cell Neurosci Neuroscience Conservation of a patient's residual hearing and prevention of fibrous tissue/new bone formation around an electrode array are some of the major challenges in cochlear implant (CI) surgery. Although it is well-known that fibrotic tissue formation around the electrode array can interfere with hearing performance in implanted patients, and that associated intracochlear inflammation can initiate loss of residual hearing, little is known about the molecular and cellular mechanisms that promote this response in the cochlea. In vitro studies in neonatal rats and in vivo studies in adult mice were performed to gain insight into the pro-inflammatory, proliferative, and remodeling phases of pathological wound healing that occur in the cochlea following an electrode analog insertion. Resident Schwann cells (SC), macrophages, and fibroblasts had a prominent role in the inflammatory process in the cochlea. Leukocytes were recruited to the cochlea following insertion of a nylon filament in adult mice, where contributed to the inflammatory response. The reparative stages in wound healing are characterized by persistent neuro-inflammation of spiral ganglion neurons (SGN) and expression of regenerative monocytes/macrophages in the cochlea. Accordingly, genes involved in extracellular matrix (ECM) deposition and remodeling were up-regulated in implanted cochleae. Maturation of scar tissue occurs in the remodeling phase of wound healing in the cochlea. Similar to other damaged peripheral nerves, M2 macrophages and de-differentiated SC were observed in damaged cochleae and may play a role in cell survival and axonal regeneration. In conclusion, the insertion of an electrode analog into the cochlea is associated with robust early and chronic inflammatory responses characterized by recruitment of leukocytes and expression of pro-inflammatory cytokines that promote intracochlear fibrosis and loss of the auditory hair cells (HC) and SGN important for hearing after CI surgery. Frontiers Media S.A. 2015-08-12 /pmc/articles/PMC4532929/ /pubmed/26321909 http://dx.doi.org/10.3389/fncel.2015.00303 Text en Copyright © 2015 Bas, Goncalves, Adams, Dinh, Bas, Van De Water and Eshraghi. 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) or licensor 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 Bas, Esperanza Goncalves, Stefania Adams, Michelle Dinh, Christine T. Bas, Jose M. Van De Water, Thomas R. Eshraghi, Adrien A. Spiral ganglion cells and macrophages initiate neuro-inflammation and scarring following cochlear implantation |
title | Spiral ganglion cells and macrophages initiate neuro-inflammation and scarring following cochlear implantation |
title_full | Spiral ganglion cells and macrophages initiate neuro-inflammation and scarring following cochlear implantation |
title_fullStr | Spiral ganglion cells and macrophages initiate neuro-inflammation and scarring following cochlear implantation |
title_full_unstemmed | Spiral ganglion cells and macrophages initiate neuro-inflammation and scarring following cochlear implantation |
title_short | Spiral ganglion cells and macrophages initiate neuro-inflammation and scarring following cochlear implantation |
title_sort | spiral ganglion cells and macrophages initiate neuro-inflammation and scarring following cochlear implantation |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532929/ https://www.ncbi.nlm.nih.gov/pubmed/26321909 http://dx.doi.org/10.3389/fncel.2015.00303 |
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