Exacerbated age-related hearing loss in mice lacking the p43 mitochondrial T3 receptor.

Age-related hearing loss Mitochondrial dysfunction Thyroid hormones p43 mitochondrial T3 receptor

Journal

BMC biology
ISSN: 1741-7007
Titre abrégé: BMC Biol
Pays: England
ID NLM: 101190720

Informations de publication

Date de publication:
01 02 2021
Historique:
received: 15 07 2020
accepted: 08 01 2021
entrez: 2 2 2021
pubmed: 3 2 2021
medline: 1 10 2021
Statut: epublish

Résumé

Age-related hearing loss (ARHL), also known as presbycusis, is the most common sensory impairment seen in elderly people. However, the cochlear aging process does not affect people uniformly, suggesting that both genetic and environmental (e.g., noise, ototoxic drugs) factors and their interaction may influence the onset and severity of ARHL. Considering the potential links between thyroid hormone, mitochondrial activity, and hearing, here, we probed the role of p43, a N-terminally truncated and ligand-binding form of the nuclear receptor TRα1, in hearing function and in the maintenance of hearing during aging in p43 We found that the p43 These results demonstrate for the first time a requirement for p43 in the maintenance of hearing during aging and highlight the need to probe the potential link between human THRA gene polymorphisms and/or mutations and accelerated age-related deafness or some adult-onset syndromic deafness.

Sections du résumé

BACKGROUND
Age-related hearing loss (ARHL), also known as presbycusis, is the most common sensory impairment seen in elderly people. However, the cochlear aging process does not affect people uniformly, suggesting that both genetic and environmental (e.g., noise, ototoxic drugs) factors and their interaction may influence the onset and severity of ARHL. Considering the potential links between thyroid hormone, mitochondrial activity, and hearing, here, we probed the role of p43, a N-terminally truncated and ligand-binding form of the nuclear receptor TRα1, in hearing function and in the maintenance of hearing during aging in p43
RESULTS
We found that the p43
CONCLUSIONS
These results demonstrate for the first time a requirement for p43 in the maintenance of hearing during aging and highlight the need to probe the potential link between human THRA gene polymorphisms and/or mutations and accelerated age-related deafness or some adult-onset syndromic deafness.

Identifiants

pubmed: 33526032
doi: 10.1186/s12915-021-00953-1
pii: 10.1186/s12915-021-00953-1
pmc: PMC7852282
doi:

Substances chimiques

Receptors, Thyroid Hormone 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

18

Subventions

Organisme : Labex EpiGenMed
ID : ANR-10-LABX-12-01
Organisme : Fondation de l'Avenir pour la Recherche Médicale Appliquée
ID : Et2-675
Organisme : Fondation Gueules Cassées
ID : 77-2017

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Auteurs

Corentin Affortit (C)

INSERM - UMR 1051, Institut des Neurosciences de Montpellier, 80 rue Augustin Fliche, 34295, Montpellier, France.
Université de Montpellier, 34000, Montpellier, France.

François Casas (F)

INRA, UMR 866 Dynamique Musculaire et Métabolisme,, 34060, Montpellier, France.

Sabine Ladrech (S)

INSERM - UMR 1051, Institut des Neurosciences de Montpellier, 80 rue Augustin Fliche, 34295, Montpellier, France.
Université de Montpellier, 34000, Montpellier, France.

Jean-Charles Ceccato (JC)

INSERM - UMR 1051, Institut des Neurosciences de Montpellier, 80 rue Augustin Fliche, 34295, Montpellier, France.
Université de Montpellier, 34000, Montpellier, France.

Jérôme Bourien (J)

INSERM - UMR 1051, Institut des Neurosciences de Montpellier, 80 rue Augustin Fliche, 34295, Montpellier, France.
Université de Montpellier, 34000, Montpellier, France.

Carolanne Coyat (C)

INSERM - UMR 1051, Institut des Neurosciences de Montpellier, 80 rue Augustin Fliche, 34295, Montpellier, France.
Université de Montpellier, 34000, Montpellier, France.

Jean-Luc Puel (JL)

INSERM - UMR 1051, Institut des Neurosciences de Montpellier, 80 rue Augustin Fliche, 34295, Montpellier, France.
Université de Montpellier, 34000, Montpellier, France.

Marc Lenoir (M)

INSERM - UMR 1051, Institut des Neurosciences de Montpellier, 80 rue Augustin Fliche, 34295, Montpellier, France.
Université de Montpellier, 34000, Montpellier, France.

Jing Wang (J)

INSERM - UMR 1051, Institut des Neurosciences de Montpellier, 80 rue Augustin Fliche, 34295, Montpellier, France. jing.wang@inserm.fr.
Université de Montpellier, 34000, Montpellier, France. jing.wang@inserm.fr.
ENT Department, CHU Montpellier, 34295, Montpellier, France. jing.wang@inserm.fr.

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