GABA co-release guides the functional maturation of glycinergic synapses in an auditory sound localization circuit

Glycinergic neurons in the brainstem and spinal cord often co-release GABA during development, but the role of this co-release in circuit refinement or synapse maturation remains poorly understood. This study found that disruption of developmental GABA co-release at the MNTB-LSO synapse, a key part of the sound localization circuit, did not affect topographic refinement by synapse elimination or strengthening. However, impaired GABA co-release prevented synapses from developing the characteristic features that enable the high-fidelity, temporally accurate transmission required for sound localization. This highlights a critical role for developmental GABA co-release in shaping the specialized functional architecture of glycinergic synapses critical for binaural processing and sound localization.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2025-12-03
DOI
https://doi.org/10.64898/2025.12.01.691682
Primary Topic
Hearing, Cochlea, Tinnitus, Genetics
Type
article
Field-Weighted Citation Impact
0.00
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article

GABA co-release guides the functional maturation of glycinergic synapses in an auditory sound localization circuit

Karl Kandler, Brian Brockway, Jongwon Lee
bioRxiv (Cold Spring Harbor Laboratory)
Hearing, Cochlea, Tinnitus, Genetics
article

GABA co-release guides the functional maturation of glycinergic synapses in an auditory sound localization circuit

Karl Kandler, Brian Brockway, Jongwon Lee
article en

Abstract

Glycinergic neurons in the brainstem and spinal cord often co-release GABA during development, but the role of this co-release in circuit refinement or synapse maturation remains poorly understood. This study found that disruption of developmental GABA co-release at the MNTB-LSO synapse, a key part of the sound localization circuit, did not affect topographic refinement by synapse elimination or strengthening. However, impaired GABA co-release prevented synapses from developing the characteristic features that enable the high-fidelity, temporally accurate transmission required for sound localization. This highlights a critical role for developmental GABA co-release in shaping the specialized functional architecture of glycinergic synapses critical for binaural processing and sound localization.

bioRxiv (Cold Spring Harbor Laboratory)
University of Pittsburgh (US)
Openalex Percentile: Top 60%
Hearing, Cochlea, Tinnitus, Genetics
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