Nav1.3 sodium channels: Rapid repriming and slow closed-state inactivationdisplay quantitative differences after expression in a mammalian cell lineand in spinal sensory neurons
Tr. Cummins et al., Nav1.3 sodium channels: Rapid repriming and slow closed-state inactivationdisplay quantitative differences after expression in a mammalian cell lineand in spinal sensory neurons, J NEUROSC, 21(16), 2001, pp. 5952-5961
Although rat brain Nav1.3 voltage-gated sodium channels have been expressed
and studied in Xenopus oocytes, these channels have not been studied after
their expression in mammalian cells. We characterized the properties of th
e rat brain Nav1.3 sodium channels expressed in human embryonic kidney (HEK
) 293 cells. Nav1.3 channels generated fast-activating and fast-inactivatin
g currents. Recovery from inactivation was relatively rapid at negative pot
entials (<-80 mV) but was slow at more positive potentials. Development of
closed-state inactivation was slow, and, as predicted on this basis, Nav1.3
channels generated large ramp currents in response to slow depolarizations
. Coexpression of <beta>3 subunits had small but significant effects on the
kinetic and voltage-dependent properties of Nav1.3 currents in HEK 293 cel
ls, but coexpression of beta1 and beta2 subunits had little or no effect on
Nav1.3 properties. Nav1.3 channels, mutated to be tetrodotoxin-resistant (
TTX-R), were expressed in SNS-null dorsal root ganglion (DRG) neurons via b
iolistics and were compared with the same construct expressed in HEK 293 ce
lls. The voltage dependence of steady-state inactivation was similar to7 mV
more depolarized in SNS-null DRG neurons, demonstrating the importance of
background cell type in determining physiological properties. Moreover, con
sistent with the idea that cellular factors can modulate the properties of
Nav1.3, the repriming kinetics were twofold faster in the neurons than in t
he HEK 293 cells. The rapid repriming of Nav1.3 suggests that it contribute
s to the acceleration of repriming of TTX-sensitive (TTX-S) sodium currents
that are seen after peripheral axotomy of DRG neurons. The relatively rapi
d recovery from inactivation and the slow closed-state inactivation kinetic
s of Nav1.3 channels suggest that neurons expressing Nav1.3 may exhibit a r
educed threshold and/or a relatively high frequency of firing.