Synaptic mitochondria regulate hair-cell synapse size and function.

Abstract

Sensory hair cells in the ear utilize specialized ribbon synapses. These synapses are defined by electron-dense presynaptic structures called ribbons, composed primarily of the structural protein Ribeye. Previous work has shown that voltage-gated influx of Ca²⁺ through Ca_V1.3 channels is critical for hair-cell synapse function and can impede ribbon formation. We show that in mature zebrafish hair cells, evoked presynaptic-Ca²⁺ influx through Ca_V1.3 channels initiates mitochondrial-Ca²⁺ (mito-Ca²⁺) uptake adjacent to ribbons. Block of mito-Ca²⁺ uptake in mature cells depresses presynaptic-Ca²⁺ influx and impacts synapse integrity. In developing zebrafish hair cells, mito-Ca²⁺ uptake coincides with spontaneous rises in presynaptic-Ca²⁺ influx. Spontaneous mito-Ca²⁺ loading lowers cellular NAD⁺/NADH redox and downregulates ribbon size. Direct application of NAD⁺ or NADH increases or decreases ribbon size respectively, possibly acting through the NAD(H)-binding domain on Ribeye. Our results present a mechanism where presynaptic- and mito-Ca²⁺ couple to confer proper presynaptic function and formation.