PT - JOURNAL ARTICLE AU - Aravind Chenrayan Govindaraju AU - Imran H. Quraishi AU - Anna Lysakowski AU - Ruth Anne Eatock AU - Robert M. Raphael TI - Nonquantal Transmission at the Vestibular Hair Cell-Calyx Synapse: K<sub>LV</sub> Currents Modulate Fast Electrical and Slow K<sup>+</sup> Potentials in the Synaptic Cleft AID - 10.1101/2021.11.18.469197 DP - 2022 Jan 01 TA - bioRxiv PG - 2021.11.18.469197 4099 - http://biorxiv.org/content/early/2022/04/29/2021.11.18.469197.short 4100 - http://biorxiv.org/content/early/2022/04/29/2021.11.18.469197.full AB - Vestibular hair cells transmit information about head position and motion across synapses to primary afferent neurons. At some of these synapses, the afferent neuron envelopes the hair cell, forming an enlarged synaptic terminal called a calyx. The vestibular hair cell-calyx synapse supports a mysterious form of electrical transmission that does not involve gap junctions termed nonquantal transmission (NQT). The NQT mechanism is thought to involve the flow of ions from the pre-synaptic hair cell to the post-synaptic calyx through low-voltage-activated channels driven by changes in cleft [K+] as K+ exits the hair cell. However, this hypothesis has not been tested with a quantitative model and the possible role of an electrical potential in the cleft has remained speculative. Here we present a computational model that captures salient experimental observations of NQT and identifies overlooked features that corroborate the existence of an electrical potential (ϕ) in the synaptic cleft. We show that changes in cleft ϕ reduce transmission latency and illustrate the relative contributions of both cleft [K+] and ϕ to the gain and phase of NQT. We further demonstrate that the magnitude and speed of NQT depend on calyx morphology and that increasing calyx height reduces action potential latency in the calyx afferent. These predictions are consistent with the idea that the calyx evolved to enhance NQT and speed up vestibular signals that drive neural circuits controlling gaze, balance, and orientation.Significance Statement The ability of the vestibular system to drive the fastest reflexes in the nervous system depends on rapid transmission of mechanosensory signals at vestibular hair cell synapses. In mammals and other amniotes, afferent neurons form unusually large calyx terminals on certain hair cells, and communication at these synapses includes nonquantal transmission (NQT), which avoids the synaptic delay of quantal transmission. We present a quantitative model that shows how NQT depends on the extent of the calyx covering the hair cell and attributes the short latency of NQT to changes in synaptic cleft electrical potential caused by current flowing through open potassium channels in the hair cell. This previously undescribed mechanism may act at other synapses.Competing Interest StatementThe authors have declared no competing interest.