Inner hair cells (IHCs) of the adult mammalian cochlea respond to sound stimuli with small and graded receptor potentials. Before the onset of hearing immature IHCs fire spontaneous Ca2+ action potentials. Both types of response lead to Ca2+ inflow through voltage-gated Ca2+ channels that causes neurotransmitter release at IHC ribbon synapses onto afferent fibres (Moser & Beutner 2000). More than 90% of the Ca2+ inflow occurs through the Cav1.3 L-type Ca2+ channels (Platzer et al. 2000), the single channel kinetics of which have yet to be determined. METHODS: Single Ca channel activity was recorded in the “cell-attached” configuration (patch-clamp technique) from the mouse immature IHCs near body temperature. Voltage steps were applied from the holding potential of –70 mV. The patch pipette solution contained 5 or 70 mM of Ba2+ as the ion carrier and Bay K 8644 to better resolve the single channel openings. RESULTS: L-type Ca channels showed a slope conductance of 39 pS and 17.6 pS in 70 and 5 mM Ba2+ respectively. The channel showed two open time constants at all voltages (at –30 mV the time constants were 0.4 and 4.9 ms with 5 mM Ba2+, and 0.4 and 1.5 ms with 70 mM Ba2+). Only the slower time constant was clearly voltage-dependent. Three closed states were found, of which only the longest was clearly voltage-dependent. Time-to-first opening distributions were fit by two time constants of which one was very fast (<1 ms). CONCLUSIONS: IHCs L-type Ca channels show multiple gating states, some of which are voltage-dependent. The kinetics properties of the single Ca2+ channels recorded in the immature IHCs are consistent with the ribbon synapses sustaining a fast and precise release onto the afferent terminal (Goutman and Glowatzki 2007).

Properties of the single calcium channels CaV1.3 in mouse cochlear inner hair cells

ZAMPINI, VALERIA;MASETTO, SERGIO;
2008-01-01

Abstract

Inner hair cells (IHCs) of the adult mammalian cochlea respond to sound stimuli with small and graded receptor potentials. Before the onset of hearing immature IHCs fire spontaneous Ca2+ action potentials. Both types of response lead to Ca2+ inflow through voltage-gated Ca2+ channels that causes neurotransmitter release at IHC ribbon synapses onto afferent fibres (Moser & Beutner 2000). More than 90% of the Ca2+ inflow occurs through the Cav1.3 L-type Ca2+ channels (Platzer et al. 2000), the single channel kinetics of which have yet to be determined. METHODS: Single Ca channel activity was recorded in the “cell-attached” configuration (patch-clamp technique) from the mouse immature IHCs near body temperature. Voltage steps were applied from the holding potential of –70 mV. The patch pipette solution contained 5 or 70 mM of Ba2+ as the ion carrier and Bay K 8644 to better resolve the single channel openings. RESULTS: L-type Ca channels showed a slope conductance of 39 pS and 17.6 pS in 70 and 5 mM Ba2+ respectively. The channel showed two open time constants at all voltages (at –30 mV the time constants were 0.4 and 4.9 ms with 5 mM Ba2+, and 0.4 and 1.5 ms with 70 mM Ba2+). Only the slower time constant was clearly voltage-dependent. Three closed states were found, of which only the longest was clearly voltage-dependent. Time-to-first opening distributions were fit by two time constants of which one was very fast (<1 ms). CONCLUSIONS: IHCs L-type Ca channels show multiple gating states, some of which are voltage-dependent. The kinetics properties of the single Ca2+ channels recorded in the immature IHCs are consistent with the ribbon synapses sustaining a fast and precise release onto the afferent terminal (Goutman and Glowatzki 2007).
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/140659
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