Phoenix auditory neurons as 3R cell model for high throughput screening of neurogenic compounds.


Journal

Hearing research
ISSN: 1878-5891
Titre abrégé: Hear Res
Pays: Netherlands
ID NLM: 7900445

Informations de publication

Date de publication:
02 2022
Historique:
received: 14 07 2021
revised: 25 10 2021
accepted: 27 10 2021
pubmed: 30 11 2021
medline: 15 3 2022
entrez: 29 11 2021
Statut: ppublish

Résumé

Auditory neurons connect the sensory hair cells from the inner ear to the brainstem. These bipolar neurons are relevant targets for pharmacological intervention aiming at protecting or improving the hearing function in various forms of sensorineural hearing loss. In the research laboratory, neurotrophic compounds are commonly used to improve survival and to promote regeneration of auditory neurons. One important roadblock delaying eventual clinical applications of these strategies in humans is the lack of powerful in vitro models allowing high throughput screening of otoprotective and regenerative compounds. The recently discovered auditory neuroprogenitors (ANPGs) derived from the A/J mouse with an unprecedented capacity to self-renew and to provide mature auditory neurons offer the possibility to overcome this bottleneck. In the present study, we further characterized the new phoenix ANPGs model and compared it to the current gold-standard spiral ganglion organotypic explant (SGE) model to assay neurite outgrowth, neurite length and glutamate-induced Ca

Identifiants

pubmed: 34844170
pii: S0378-5955(21)00225-2
doi: 10.1016/j.heares.2021.108391
pii:
doi:

Substances chimiques

Brain-Derived Neurotrophic Factor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

108391

Subventions

Organisme : Austrian Science Fund FWF
ID : I 3154
Pays : Austria

Informations de copyright

Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Francis Rousset (F)

The Inner Ear & Olfaction Lab, Department of Pathology and Immunology, Faculty of Medicine, University of Geneva, Switzerland. Electronic address: Francis.Rousset@unige.ch.

Dominik Schmidbauer (D)

Inner Ear Laboratory, Department of Otolaryngology, Medical University of Innsbruck, Austria.

Stefan Fink (S)

Translational Hearing Research, Tübingen Hearing Research Center, Department of Otolaryngology, Head & Neck Surgery, University of Tübingen, Germany.

Youssef Adel (Y)

Translational Hearing Research, Tübingen Hearing Research Center, Department of Otolaryngology, Head & Neck Surgery, University of Tübingen, Germany.

Benjamin Obexer (B)

Inner Ear Laboratory, Department of Otolaryngology, Medical University of Innsbruck, Austria.

Marcus Müller (M)

Translational Hearing Research, Tübingen Hearing Research Center, Department of Otolaryngology, Head & Neck Surgery, University of Tübingen, Germany.

Rudolf Glueckert (R)

Inner Ear Laboratory, Department of Otolaryngology, Medical University of Innsbruck, Austria. Electronic address: rudolf.glueckert@i-med.ac.at.

Hubert Löwenheim (H)

Translational Hearing Research, Tübingen Hearing Research Center, Department of Otolaryngology, Head & Neck Surgery, University of Tübingen, Germany.

Pascal Senn (P)

The Inner Ear & Olfaction Lab, Department of Pathology and Immunology, Faculty of Medicine, University of Geneva, Switzerland; Department of Clinical Neurosciences, Service of ORL & Head and Neck Surgery, University Hospital of Geneva, Switzerland.

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Classifications MeSH