In vivo spontaneous Ca2+ activity in the pre-hearing mammalian cochlea

Abstract The refinement of neural circuits towards mature function is driven during development by patterned spontaneous calcium-dependent electrical activity. In the auditory system, this sensory-independent activity arises in the pre-hearing cochlea and regulates the survival and refinement of the...

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Main Authors: Francesca De Faveri, Federico Ceriani, Walter Marcotti
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-024-55519-w
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author Francesca De Faveri
Federico Ceriani
Walter Marcotti
author_facet Francesca De Faveri
Federico Ceriani
Walter Marcotti
author_sort Francesca De Faveri
collection DOAJ
description Abstract The refinement of neural circuits towards mature function is driven during development by patterned spontaneous calcium-dependent electrical activity. In the auditory system, this sensory-independent activity arises in the pre-hearing cochlea and regulates the survival and refinement of the auditory pathway. However, the origin and interplay of calcium signals during cochlear development is unknown in vivo. Here we show how calcium dynamics in the cochlear neuroepithelium of live pre-hearing mice shape the activity of the inner hair cells (IHCs) and their afferent synapses. Both IHCs and supporting cells (SCs) generate spontaneous calcium-dependent activity. Calcium waves from SCs synchronise the activity of nearby IHCs, which then spreads longitudinally recruiting several additional IHCs via a calcium wave-independent mechanism. This synchronised IHC activity in vivo increases the probability of afferent terminal recruitment. Moreover, the modiolar-to-pillar segregation in sound sensitivity of mature auditory nerve fibres appears to be primed at pre-hearing ages.
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spelling doaj-art-8baad9ca7b2d4fcb87b5ea5fd86398062025-01-05T12:36:54ZengNature PortfolioNature Communications2041-17232025-01-0116111410.1038/s41467-024-55519-wIn vivo spontaneous Ca2+ activity in the pre-hearing mammalian cochleaFrancesca De Faveri0Federico Ceriani1Walter Marcotti2School of Biosciences, University of SheffieldSchool of Biosciences, University of SheffieldSchool of Biosciences, University of SheffieldAbstract The refinement of neural circuits towards mature function is driven during development by patterned spontaneous calcium-dependent electrical activity. In the auditory system, this sensory-independent activity arises in the pre-hearing cochlea and regulates the survival and refinement of the auditory pathway. However, the origin and interplay of calcium signals during cochlear development is unknown in vivo. Here we show how calcium dynamics in the cochlear neuroepithelium of live pre-hearing mice shape the activity of the inner hair cells (IHCs) and their afferent synapses. Both IHCs and supporting cells (SCs) generate spontaneous calcium-dependent activity. Calcium waves from SCs synchronise the activity of nearby IHCs, which then spreads longitudinally recruiting several additional IHCs via a calcium wave-independent mechanism. This synchronised IHC activity in vivo increases the probability of afferent terminal recruitment. Moreover, the modiolar-to-pillar segregation in sound sensitivity of mature auditory nerve fibres appears to be primed at pre-hearing ages.https://doi.org/10.1038/s41467-024-55519-w
spellingShingle Francesca De Faveri
Federico Ceriani
Walter Marcotti
In vivo spontaneous Ca2+ activity in the pre-hearing mammalian cochlea
Nature Communications
title In vivo spontaneous Ca2+ activity in the pre-hearing mammalian cochlea
title_full In vivo spontaneous Ca2+ activity in the pre-hearing mammalian cochlea
title_fullStr In vivo spontaneous Ca2+ activity in the pre-hearing mammalian cochlea
title_full_unstemmed In vivo spontaneous Ca2+ activity in the pre-hearing mammalian cochlea
title_short In vivo spontaneous Ca2+ activity in the pre-hearing mammalian cochlea
title_sort in vivo spontaneous ca2 activity in the pre hearing mammalian cochlea
url https://doi.org/10.1038/s41467-024-55519-w
work_keys_str_mv AT francescadefaveri invivospontaneousca2activityintheprehearingmammaliancochlea
AT federicoceriani invivospontaneousca2activityintheprehearingmammaliancochlea
AT waltermarcotti invivospontaneousca2activityintheprehearingmammaliancochlea