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   <subfield code="a">Potassium accumulation between type I hair cells and calyx terminals in mouse crista</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Rebecca Lim, Angela Kindig, Scott Donne, Robert Callister, Alan Brichta]</subfield>
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   <subfield code="a">The mode of synaptic transmission in the vestibular periphery, between type I hair cells and their associated calyx terminal, has been the subject of much debate. The close and extensive apposition of pre- and post-synaptic elements has led some to suggest potassium (K+) accumulates in the intercellular space and even plays a role in synaptic transmission. During patch clamp recordings from isolated and embedded hair cells in a semi-intact preparation of the mouse cristae, we noted marked differences in whole-cell currents. Embedded type I hair cells show a prominent droop during steady-state activation as well as a dramatic collapse in tail currents. Responses to a depolarizing voltage step (−124 to +16mV) in embedded, but not isolated, hair cells resulted in a &gt;40mV shift of the K+ equilibrium potential and a rise in effective K+ concentration (&gt;50mM) in the intercellular space. Together these data suggest K+ accumulation in the intercellular space accounts for the different responses in isolated and embedded type I hair cells. To test this notion, we exposed the preparation to hyperosmotic solutions to enlarge the intercellular space. As predicted, the K+ accumulation effects were reduced; however, a fit of our data with a classic diffusion model suggested K+ permeability, rather than the intercellular space, had been altered by the hyperosmotic change. These results support the notion that under depolarizing conditions substantial K+ accumulation occurs in the space between type I hair cells and calyx. The extent of K+ accumulation during normal synaptic transmission, however, remains to be determined.</subfield>
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