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J Neurophysiol 91: 2422-2428, 2004. First published January 28, 2004; doi:10.1152/jn.01130.2003
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Large Releasable Pool of Synaptic Vesicles in Chick Cochlear Hair Cells

Marc D. Eisen2, Maria Spassova1 and Thomas D. Parsons1,2

1 Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, Kennett Square, 19348; 2 Department of Otorhinolaryngology, Head and Neck Surgery, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104

Submitted 24 November 2003; accepted in final form 13 January 2004

Hearing requires the hair cell synapse to maintain notable temporal fidelity (<=1 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.


Address for reprint requests and other correspondence: T. D. Parsons, Department of Clinical Studies, New Bolton Center, University of Pennsylvania School of Veterinary Medicine, 382 West Street Rd., Kennett Square, PA 19348 (E-mail: thd{at}vet.upenn.edu).




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