Pathophysiological changes in inner hair cell ribbon synapses in the ageing mammalian cochlea.

age-related hearing loss auditory brainstem responses calcium channels cochlea exocytosis inner hair cells mouse ribbon synapses

Journal

The Journal of physiology
ISSN: 1469-7793
Titre abrégé: J Physiol
Pays: England
ID NLM: 0266262

Informations de publication

Date de publication:
10 2020
Historique:
received: 24 04 2020
accepted: 24 07 2020
pubmed: 28 7 2020
medline: 16 2 2021
entrez: 26 7 2020
Statut: ppublish

Résumé

Age-related hearing loss (ARHL) is associated with the loss of inner hair cell (IHC) ribbon synapses, lower hearing sensitivity and decreased ability to understand speech, especially in a noisy environment. Little is known about the age-related physiological and morphological changes that occur at ribbon synapses. We show that the differing degrees of ARHL in four selected mouse stains is correlated with the loss of ribbon synapses, being most severe for the strains C57BL/6NTac and C57BL/6J, less so for C57BL/6NTac Mammalian cochlear inner hair cells (IHCs) are specialized sensory receptors able to provide dynamic coding of sound signals. This ability is largely conferred by their ribbon synapses, which tether a large number of vesicles at the IHC's presynaptic active zones, allowing high rates of sustained synaptic transmission onto the afferent fibres. How the physiological and morphological properties of ribbon synapses change with age remains largely unknown. Here, we have investigated the biophysical and morphological properties of IHC ribbon synapses in the ageing cochlea (9-12 kHz region) of four mouse strains commonly used in hearing research: early-onset progressive hearing loss (C57BL/6J and C57BL/6NTac) and 'good hearing' strains (C57BL/6NTac

Identifiants

pubmed: 32710572
doi: 10.1113/JP280018
pmc: PMC7612121
mid: EMS140587
doi:

Substances chimiques

Cadherins 0
Cdh23 protein, mouse 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

4339-4355

Subventions

Organisme : Medical Research Council
ID : MR/S002510/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UP_1503/2
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 102892/Z/13/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC/UP/1503/2
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 102892
Pays : United Kingdom

Informations de copyright

© 2020 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society.

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Auteurs

Jing-Yi Jeng (JY)

Department of Biomedical Science, University of Sheffield, Sheffield, S10 2TN, UK.
Neuroscience Institute, University of Sheffield, Sheffield, S10 2TN, UK.

Federico Ceriani (F)

Department of Biomedical Science, University of Sheffield, Sheffield, S10 2TN, UK.
Neuroscience Institute, University of Sheffield, Sheffield, S10 2TN, UK.

Jennifer Olt (J)

Department of Biomedical Science, University of Sheffield, Sheffield, S10 2TN, UK.

Steve D M Brown (SDM)

Mammalian Genetics Unit, MRC Harwell Institute, Oxfordshire, UK.

Matthew C Holley (MC)

Department of Biomedical Science, University of Sheffield, Sheffield, S10 2TN, UK.

Michael R Bowl (MR)

Mammalian Genetics Unit, MRC Harwell Institute, Oxfordshire, UK.

Stuart L Johnson (SL)

Department of Biomedical Science, University of Sheffield, Sheffield, S10 2TN, UK.
Neuroscience Institute, University of Sheffield, Sheffield, S10 2TN, UK.

Walter Marcotti (W)

Department of Biomedical Science, University of Sheffield, Sheffield, S10 2TN, UK.
Neuroscience Institute, University of Sheffield, Sheffield, S10 2TN, UK.

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