Elementary properties of CaV1.3 Ca2+ channels expressed in mouse cochlear inner hair cells

Valeria Zampini, Stuart Leigh Johnson, Christoph Franz, Neil D. Lawrence, Stefan Muenkner Jutta Engel, Marlies Knipper, Jacopo Magistretti, Sergio Masetto, Walter Marcotti
,  588:187-189, 2010.

Abstract

Mammalian cochlear inner hair cells (IHCs) are specialized to process developmental signals during immature stages and sound stimuli in adult animals. These signals are conveyed onto auditory afferent nerve fibres. Neurotransmitter release at IHC ribbon synapses is controlled by L-type CaV1.3 Ca2+ channels, the biophysics of which are still unknown in native mammalian cells. We have investigated the localization and elementary properties of Ca2+ channels in immature mouse IHCs under near-physiological recording conditions. CaV1.3 Ca2+ channels at the cell pre-synaptic site co-localize with about half of the total number of ribbons present in immature IHCs. These channels activated at relatively hyperpolarized membrane potentials (about -70 mV), showed a relatively short first latency and weak inactivation, which would allow IHCs to generate and accurately encode spontaneous Ca2+ action potential activity characteristic of these immature cells. The CaV1.3 Ca2+ channels showed a very low open probability (about 0.15 at -20 mV: near the peak of an action potential). Comparison of elementary and macroscopic Ca2+ currents indicated that very few Ca2+ channels are associated with each docked vesicle at IHC ribbon synapses. Finally, we found that the open probability of Ca2+ channels, but not their opening time, was voltage dependent. This finding provides a possible correlation between presynaptic Ca2+ channel properties and the characteristic frequency/amplitude of EPSCs in auditory afferent fibres.

Cite this Paper


BibTeX
@InProceedings{pmlr-v-zampini-elementary09, title = {Elementary properties of CaV1.3 Ca2+ channels expressed in mouse cochlear inner hair cells}, author = {Valeria Zampini and Stuart Leigh Johnson and Christoph Franz and Neil D. Lawrence and Stefan Muenkner Jutta Engel and Marlies Knipper and Jacopo Magistretti and Sergio Masetto and Walter Marcotti}, pages = {187--189}, year = {}, editor = {}, volume = {588}, url = {http://inverseprobability.com/publications/zampini-elementary09.html}, abstract = {Mammalian cochlear inner hair cells (IHCs) are specialized to process developmental signals during immature stages and sound stimuli in adult animals. These signals are conveyed onto auditory afferent nerve fibres. Neurotransmitter release at IHC ribbon synapses is controlled by L-type CaV1.3 Ca2+ channels, the biophysics of which are still unknown in native mammalian cells. We have investigated the localization and elementary properties of Ca2+ channels in immature mouse IHCs under near-physiological recording conditions. CaV1.3 Ca2+ channels at the cell pre-synaptic site co-localize with about half of the total number of ribbons present in immature IHCs. These channels activated at relatively hyperpolarized membrane potentials (about -70 mV), showed a relatively short first latency and weak inactivation, which would allow IHCs to generate and accurately encode spontaneous Ca2+ action potential activity characteristic of these immature cells. The CaV1.3 Ca2+ channels showed a very low open probability (about 0.15 at -20 mV: near the peak of an action potential). Comparison of elementary and macroscopic Ca2+ currents indicated that very few Ca2+ channels are associated with each docked vesicle at IHC ribbon synapses. Finally, we found that the open probability of Ca2+ channels, but not their opening time, was voltage dependent. This finding provides a possible correlation between presynaptic Ca2+ channel properties and the characteristic frequency/amplitude of EPSCs in auditory afferent fibres.} }
Endnote
%0 Conference Paper %T Elementary properties of CaV1.3 Ca2+ channels expressed in mouse cochlear inner hair cells %A Valeria Zampini %A Stuart Leigh Johnson %A Christoph Franz %A Neil D. Lawrence %A Stefan Muenkner Jutta Engel %A Marlies Knipper %A Jacopo Magistretti %A Sergio Masetto %A Walter Marcotti %B %C Proceedings of Machine Learning Research %D %E %F pmlr-v-zampini-elementary09 %I PMLR %J Proceedings of Machine Learning Research %P 187--189 %R 10.1113/jphysiol.2009.181917 %U http://inverseprobability.com %V %W PMLR %X Mammalian cochlear inner hair cells (IHCs) are specialized to process developmental signals during immature stages and sound stimuli in adult animals. These signals are conveyed onto auditory afferent nerve fibres. Neurotransmitter release at IHC ribbon synapses is controlled by L-type CaV1.3 Ca2+ channels, the biophysics of which are still unknown in native mammalian cells. We have investigated the localization and elementary properties of Ca2+ channels in immature mouse IHCs under near-physiological recording conditions. CaV1.3 Ca2+ channels at the cell pre-synaptic site co-localize with about half of the total number of ribbons present in immature IHCs. These channels activated at relatively hyperpolarized membrane potentials (about -70 mV), showed a relatively short first latency and weak inactivation, which would allow IHCs to generate and accurately encode spontaneous Ca2+ action potential activity characteristic of these immature cells. The CaV1.3 Ca2+ channels showed a very low open probability (about 0.15 at -20 mV: near the peak of an action potential). Comparison of elementary and macroscopic Ca2+ currents indicated that very few Ca2+ channels are associated with each docked vesicle at IHC ribbon synapses. Finally, we found that the open probability of Ca2+ channels, but not their opening time, was voltage dependent. This finding provides a possible correlation between presynaptic Ca2+ channel properties and the characteristic frequency/amplitude of EPSCs in auditory afferent fibres.
RIS
TY - CPAPER TI - Elementary properties of CaV1.3 Ca2+ channels expressed in mouse cochlear inner hair cells AU - Valeria Zampini AU - Stuart Leigh Johnson AU - Christoph Franz AU - Neil D. Lawrence AU - Stefan Muenkner Jutta Engel AU - Marlies Knipper AU - Jacopo Magistretti AU - Sergio Masetto AU - Walter Marcotti BT - PY - DA - ED - ID - pmlr-v-zampini-elementary09 PB - PMLR SP - 187 DP - PMLR EP - 189 DO - 10.1113/jphysiol.2009.181917 L1 - UR - http://inverseprobability.com/publications/zampini-elementary09.html AB - Mammalian cochlear inner hair cells (IHCs) are specialized to process developmental signals during immature stages and sound stimuli in adult animals. These signals are conveyed onto auditory afferent nerve fibres. Neurotransmitter release at IHC ribbon synapses is controlled by L-type CaV1.3 Ca2+ channels, the biophysics of which are still unknown in native mammalian cells. We have investigated the localization and elementary properties of Ca2+ channels in immature mouse IHCs under near-physiological recording conditions. CaV1.3 Ca2+ channels at the cell pre-synaptic site co-localize with about half of the total number of ribbons present in immature IHCs. These channels activated at relatively hyperpolarized membrane potentials (about -70 mV), showed a relatively short first latency and weak inactivation, which would allow IHCs to generate and accurately encode spontaneous Ca2+ action potential activity characteristic of these immature cells. The CaV1.3 Ca2+ channels showed a very low open probability (about 0.15 at -20 mV: near the peak of an action potential). Comparison of elementary and macroscopic Ca2+ currents indicated that very few Ca2+ channels are associated with each docked vesicle at IHC ribbon synapses. Finally, we found that the open probability of Ca2+ channels, but not their opening time, was voltage dependent. This finding provides a possible correlation between presynaptic Ca2+ channel properties and the characteristic frequency/amplitude of EPSCs in auditory afferent fibres. ER -
APA
Zampini, V., Johnson, S.L., Franz, C., Lawrence, N.D., Engel, S.M.J., Knipper, M., Magistretti, J., Masetto, S. & Marcotti, W.. (). Elementary properties of CaV1.3 Ca2+ channels expressed in mouse cochlear inner hair cells. , in PMLR :187-189

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