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Decellularized equine carotid artery layers as matrix for regenerated neurites of spiral ganglion neurons

Today’s best solution in compensating for sensorineural hearing loss is the cochlear implant, which electrically stimulates the spiral ganglion neurons in the inner ear. An optimum hearing impression is not ensured due to, among other reasons, a remaining anatomical gap between the spiral ganglion n...

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Autores principales: Yilmaz-Bayraktar, Suheda, Schwieger, Jana, Scheper, Verena, Lenarz, Thomas, Böer, Ulrike, Kreienmeyer, Michaela, Torrente, Mariela, Doll, Theodor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221869/
https://www.ncbi.nlm.nih.gov/pubmed/31434531
http://dx.doi.org/10.1177/0391398819868481
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author Yilmaz-Bayraktar, Suheda
Schwieger, Jana
Scheper, Verena
Lenarz, Thomas
Böer, Ulrike
Kreienmeyer, Michaela
Torrente, Mariela
Doll, Theodor
author_facet Yilmaz-Bayraktar, Suheda
Schwieger, Jana
Scheper, Verena
Lenarz, Thomas
Böer, Ulrike
Kreienmeyer, Michaela
Torrente, Mariela
Doll, Theodor
author_sort Yilmaz-Bayraktar, Suheda
collection PubMed
description Today’s best solution in compensating for sensorineural hearing loss is the cochlear implant, which electrically stimulates the spiral ganglion neurons in the inner ear. An optimum hearing impression is not ensured due to, among other reasons, a remaining anatomical gap between the spiral ganglion neurons and the implant electrodes. The gap could be bridged via pharmacologically triggered neurite growth toward the electrodes if biomaterials for neurite guidance could be provided. For this, we investigated the suitability of decellularized tissue. We compared three different layers (tunica adventitia, tunica media, and tunica intima) of decellularized equine carotid arteries in a preliminary approach. Rat spiral ganglia explants were cultured on decellularized equine carotid artery layers and neurite sprouting was assessed quantitatively. Generally, neurite outgrowth was possible and it was most prominent on the intima (in average 83 neurites per spiral ganglia explants, followed by the adventitia (62 neurites) and the lowest growth on the media (20 neurites). Thus, decellularized equine carotid arteries showed promising effects on neurite regeneration and can be developed further as efficient biomaterials for neural implants in hearing research.
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spelling pubmed-72218692020-06-02 Decellularized equine carotid artery layers as matrix for regenerated neurites of spiral ganglion neurons Yilmaz-Bayraktar, Suheda Schwieger, Jana Scheper, Verena Lenarz, Thomas Böer, Ulrike Kreienmeyer, Michaela Torrente, Mariela Doll, Theodor Int J Artif Organs Original Research Articles Today’s best solution in compensating for sensorineural hearing loss is the cochlear implant, which electrically stimulates the spiral ganglion neurons in the inner ear. An optimum hearing impression is not ensured due to, among other reasons, a remaining anatomical gap between the spiral ganglion neurons and the implant electrodes. The gap could be bridged via pharmacologically triggered neurite growth toward the electrodes if biomaterials for neurite guidance could be provided. For this, we investigated the suitability of decellularized tissue. We compared three different layers (tunica adventitia, tunica media, and tunica intima) of decellularized equine carotid arteries in a preliminary approach. Rat spiral ganglia explants were cultured on decellularized equine carotid artery layers and neurite sprouting was assessed quantitatively. Generally, neurite outgrowth was possible and it was most prominent on the intima (in average 83 neurites per spiral ganglia explants, followed by the adventitia (62 neurites) and the lowest growth on the media (20 neurites). Thus, decellularized equine carotid arteries showed promising effects on neurite regeneration and can be developed further as efficient biomaterials for neural implants in hearing research. SAGE Publications 2019-08-22 2020-05 /pmc/articles/PMC7221869/ /pubmed/31434531 http://dx.doi.org/10.1177/0391398819868481 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Articles
Yilmaz-Bayraktar, Suheda
Schwieger, Jana
Scheper, Verena
Lenarz, Thomas
Böer, Ulrike
Kreienmeyer, Michaela
Torrente, Mariela
Doll, Theodor
Decellularized equine carotid artery layers as matrix for regenerated neurites of spiral ganglion neurons
title Decellularized equine carotid artery layers as matrix for regenerated neurites of spiral ganglion neurons
title_full Decellularized equine carotid artery layers as matrix for regenerated neurites of spiral ganglion neurons
title_fullStr Decellularized equine carotid artery layers as matrix for regenerated neurites of spiral ganglion neurons
title_full_unstemmed Decellularized equine carotid artery layers as matrix for regenerated neurites of spiral ganglion neurons
title_short Decellularized equine carotid artery layers as matrix for regenerated neurites of spiral ganglion neurons
title_sort decellularized equine carotid artery layers as matrix for regenerated neurites of spiral ganglion neurons
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221869/
https://www.ncbi.nlm.nih.gov/pubmed/31434531
http://dx.doi.org/10.1177/0391398819868481
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