Spontaneous Calcium Signalling in the Developing Mammalian Cochlea

In mammals, the accurate and high-fidelity representation of sound largely depends on the cochlea, the sensory organ specialized for transducing acoustic signals into neural activity with remarkable temporal precision. Prior to hearing onset, which occurs around postnatal day 12 in most altricial rodents, the immature cochlea plays an active role in the refinement of neural circuits along the auditory pathway. To accomplish this function, sensory hair cells and glia-like supporting cells in the immature cochlea generate distinct patterns of spontaneous Ca<sup>2+</sup> signals. Synchronized Ca<sup>2+</sup>-dependent activity across multiple hair cells is conveyed to the ascending auditory neurons, where it contributes to the emergence of tonotopic maps that enable frequency discrimination. Within the cochlea itself, this spontaneous Ca<sup>2+</sup> activity serves to promote cellular and synaptic refinement. In this review, we summarize the current insights into the cellular and molecular mechanisms responsible for generating and modulating these spontaneous Ca<sup>2+</sup> signals in the developing cochlea, and how they regulate the activation of auditory afferent fibres.

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Publication Details

Journal
Journal of the Association for Research in Otolaryngology
Published
2026-02-23
DOI
https://doi.org/10.1007/s10162-026-01035-1
Primary Topic
Hearing, Cochlea, Tinnitus, Genetics
Type
article
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article

Spontaneous Calcium Signalling in the Developing Mammalian Cochlea

Federico Ceriani, Walter Marcotti
Journal of the Association for Research in Otolaryngology
Hearing, Cochlea, Tinnitus, Genetics
article

Spontaneous Calcium Signalling in the Developing Mammalian Cochlea

Federico Ceriani, Walter Marcotti
article en

Abstract

In mammals, the accurate and high-fidelity representation of sound largely depends on the cochlea, the sensory organ specialized for transducing acoustic signals into neural activity with remarkable temporal precision. Prior to hearing onset, which occurs around postnatal day 12 in most altricial rodents, the immature cochlea plays an active role in the refinement of neural circuits along the auditory pathway. To accomplish this function, sensory hair cells and glia-like supporting cells in the immature cochlea generate distinct patterns of spontaneous Ca<sup>2+</sup> signals. Synchronized Ca<sup>2+</sup>-dependent activity across multiple hair cells is conveyed to the ascending auditory neurons, where it contributes to the emergence of tonotopic maps that enable frequency discrimination. Within the cochlea itself, this spontaneous Ca<sup>2+</sup> activity serves to promote cellular and synaptic refinement. In this review, we summarize the current insights into the cellular and molecular mechanisms responsible for generating and modulating these spontaneous Ca<sup>2+</sup> signals in the developing cochlea, and how they regulate the activation of auditory afferent fibres.

Journal of the Association for Research in Otolaryngology
University of Sheffield (GB)
Reduced inequalities, Peace, Justice and strong institutions
Openalex Percentile: Top 42%
Hearing, Cochlea, Tinnitus, Genetics
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