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1H T-type calcium channels in excitability of mouse embryonic primary vestibular neurones
1 Institut des Neurosciences de Montpellier, INSERM U583, Hôpital Saint Eloi, 80 rue Augustin Fliche, 34091 Montpellier cedex 5, France
2 Institut de Génomique Fonctionnelle, CNRS UMR 5203, INSERM U661, 141 rue de la Cardonille, 34094 Montpellier cedex 5, France
Ca2+ influx through voltage-gated calcium channels probably influences neuronal ontogenesis. Many developing neurones transiently express T-type/Cav3 calcium channels that contribute to their electrical activity and potentially to their morphological differentiation. Here we have characterized the electrophysiological properties and the functional role of a large T-type calcium current that is present in mouse developing primary vestibular neurones at embryonic day E17. This T-type current showed fast activation and inactivation, as well as slow deactivation kinetics. The overlap of activation and inactivation parameters produced a window current between 65 and 45 mV. Recovery from short-term inactivation was slow suggesting the presence of the Cav3.2 subunit. This T-type current was blocked by micromolar concentrations of Ni2+ and was inhibited by fast perfusion velocities in a similar fashion to recombinant Cav3.2 T-type channels expressed in HEK-293 cells. More importantly, current clamp experiments have revealed that the T-current could elicit afterdepolarization potentials during the repolarization phase of action potentials, and occasionally generate calcium spikes. Taken together, we demonstrate that the Cav3.2 subunit is likely to be the main T-type calcium channel subunit expressed in embryonic vestibular neurones and should play a key role in the excitability of these neurones during the ontogenesis of vestibular afferentation.
(Received 26 April 2005;
accepted after revision 15 June 2005;
first published online 16 June 2005)
Corresponding author G. Desmadryl: INSERM U583, INM, Hôpital Saint Eloi, 80 rue Augustin Fliche, 34091 Montpellier cedex 5, France. Email: desmad{at}univ-montp2.fr
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