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Acta Physiologica 2008; Volume 194, Supplement 665
The 59th National Congress of the Italian Physiological Society
9/17/2008-9/19/2008
Cagliari, Italy
PROPERTIES OF THE CAV1.3 CALCIUM CHANNELS EXPRESSED IN MOUSE COCHLEAR INNER HAIR CELLS SYNAPSES
Abstract number: P149
ZAMPINI1 V, JOHNSON2 SL, MARCOTTI2 W, ZUCCA1 G, MASETTO1 S
1Dip. Scienze Fisiologiche-Farmacologiche Cellulari-Molecolari, Universit degli studi di Pavia, Italy
2Dept. of Biomedical Science, University of Sheffield, [email protected]
Aim:
Voltage-dependent L-type Ca2+ channels (CaV1.3) are expressed at the inner hair cells (IHCs) ribbon synapse, the primary sensory receptors of the mammalian cochlea, and trigger the afferent transmission in response to spontaneous Ca2+ action potentials during pre-hearing stages of development. The elementary properties of these Ca2+ channels have yet to be determined.
Methods:
Single Ca2+ channel activity was recorded from mouse apical-coil IHCs (postnatal day 59) near body temperature using the "cell-attached" configuration of the patch-clamp technique. The patch pipette solution contained 5 mM of Ba2+ as the ion carrier and Bay K 8644 to resolve the single channel openings.
Results:
L-type Ca2+ channel activity was already detectable at membrane voltages around 70 mV. The single channel slope conductance was 18 pS. The open probability (Po) was strictly voltage-dependent and increased with depolarization, reaching a maximum value of about 0.23. The percentage of null-sweeps was significantly high (on average >80%) at all membrane potentials. The average single channel Ba2+ current showed slow inactivation.
Conclusions:
The results are consistent with cochlear IHCs expressing CaV1.3 Ca channels. Since the voltage activation threshold is well in the range of the presumed IHCs resting membrane potential, the resulting Ca2+ inflow would support both the spontaneous Ca2+ action potential activity characteristic of pre-hearing IHCs (Marcotti et al. 2003, J Physiol 52:743761), and the spontaneous neurotransmitter release onto the auditory afferent nerve fibers.
Supported by MIUR, Rome, Italy, and The Royal Society, The Wellcome Trust and Deafness Research, UK.
To cite this abstract, please use the following information:
Acta Physiologica 2008; Volume 194, Supplement 665 :P149