Journal
JOURNAL OF NEUROPHYSIOLOGY
Volume 91, Issue 6, Pages 2422-2428Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/jn.01130.2003
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- NIDCD NIH HHS [DC 03763] Funding Source: Medline
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Hearing requires the hair cell synapse to maintain notable temporal fidelity (less than or equal to1 ms) while sustaining neurotransmitter release for prolonged periods of time ( minutes). Here we probed the properties and possible anatomical substrate of prolonged neurotransmitter release by using electrical measures of cell surface area as a proxy for neurotransmitter release to study hair cell exocytosis evoked by repetitive stimuli. We observed marked depression of exocytosis by chick tall hair cells. This exocytic depression cannot be explained by calcium current inactivation, presynaptic autoinhibition by metabotropic glutamate receptors, or postsynaptic receptor desensitization. Rather, cochlear hair cell exocytic depression resulted from the exhaustion of a functional vesicle pool. This releasable vesicle pool is large, totaling approximately 8,000 vesicles, and is nearly 10 times greater than the number of vesicles tethered to synaptic ribbons. Such a large functional pool suggests the recruitment of cytoplasmic vesicles to sustain exocytosis, important for maintaining prolonged, high rates of neural activity needed to encode sound.
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