Diversity matters — extending sound intensity coding by inner hair cells via heterogeneous synapses

Author:

Moser Tobias123ORCID,Karagulyan Nare124,Neef Jakob12ORCID,Jaime Tobón Lina María124ORCID

Affiliation:

1. Institute for Auditory Neuroscience and InnerEarLab University Medical Center Göttingen Göttingen Germany

2. Auditory Neuroscience and Synaptic Nanophysiology Group Max Planck Institute for Multidisciplinary Sciences Göttingen Germany

3. Cluster of Excellence “Multiscale Bioimaging of Excitable Cells” Göttingen Germany

4. Hertha Sponer College Cluster of Excellence “Multiscale Bioimaging of Excitable Cells” Cluster of Excellence Göttingen Germany

Abstract

AbstractOur sense of hearing enables the processing of stimuli that differ in sound pressure by more than six orders of magnitude. How to process a wide range of stimulus intensities with temporal precision is an enigmatic phenomenon of the auditory system. Downstream of dynamic range compression by active cochlear micromechanics, the inner hair cells (IHCs) cover the full intensity range of sound input. Yet, the firing rate in each of their postsynaptic spiral ganglion neurons (SGNs) encodes only a fraction of it. As a population, spiral ganglion neurons with their respective individual coding fractions cover the entire audible range. How such “dynamic range fractionation” arises is a topic of current research and the focus of this review. Here, we discuss mechanisms for generating the diverse functional properties of SGNs and formulate testable hypotheses. We postulate that an interplay of synaptic heterogeneity, molecularly distinct subtypes of SGNs, and efferent modulation serves the neural decomposition of sound information and thus contributes to a population code for sound intensity.

Publisher

Springer Science and Business Media LLC

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

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