Nonquantal transmission at the vestibular hair cell–calyx synapse: K LV currents modulate fast electrical and slow K + potentials

Author:

Govindaraju Aravind Chenrayan12ORCID,Quraishi Imran H.3ORCID,Lysakowski Anna4ORCID,Eatock Ruth Anne5ORCID,Raphael Robert M.2ORCID

Affiliation:

1. Applied Physics Graduate Program, Smalley-Curl Institute, Rice University, Houston, TX 77005

2. Department of Bioengineering, Rice University, Houston, TX 77005

3. Department of Neurology, Yale University School of Medicine, New Haven, CT 06510

4. Department of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL 60612

5. Department of Neurobiology, University of Chicago, Chicago, IL 60637

Abstract

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 presynaptic hair cell to the postsynaptic 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 experimental observations of NQT and identifies features that support 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.

Funder

HHS | NIH | National Institute on Deafness and Other Communication Disorders

Hearing Health Foundation

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference55 articles.

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