Functional properties and differential neuromodulation of Nav1.6 channels

被引:96
作者
Chen, Yuan [1 ]
Yu, Frank H. [1 ]
Sharp, Elizabeth M. [1 ]
Beacham, Daniel [1 ]
Scheuer, Todd [1 ]
Catterall, William A. [1 ]
机构
[1] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
关键词
D O I
10.1016/j.mcn.2008.05.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The voltage-gated sodium channel Na(v)1.6 plays unique roles in the nervous system, but its functional properties and neuromodulation are not as well established as for Na(v)1.2 channels. We found no significant differences in voltage-dependent activation or fast inactivation between Na(v)1.6 and Na(v)1.2 channels expressed in non-excitable cells. In contrast, the voltage dependence of slow inactivation was more positive for Na(v)1.6 channels, they conducted substantially larger persistent sodium Currents than Na(v)1.2 channels, and they were much less sensitive to inhibition by phosphorylation by cAMP-dependent protein kinase and protein kinase C. Resurgent sodium current, a hallmark of Na(v)1.6 channels in neurons, was not observed for Na(v)1.6 expressed alone or with the auxiliary beta(4) subunit. The unique properties of Nav1.6 channels, together with the resurgent currents that they conduct in neurons, make these channels well-suited to provide the driving force for sustained repetitive firing, a crucial property of neurons. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:607 / 615
页数:9
相关论文
共 86 条
[31]   Voltage-gated sodium channels shape subthreshold EPSPs in layer 5 pyramidal neurons from rat prefrontal cortex [J].
González-Burgos, G ;
Barrionuevo, G .
JOURNAL OF NEUROPHYSIOLOGY, 2001, 86 (04) :1671-1684
[32]   Open-channel block by the cytoplasmic tail of sodium channel β4 as a mechanism for resurgent sodium current [J].
Grieco, TM ;
Malhotra, JD ;
Chen, C ;
Isom, LL ;
Raman, IM .
NEURON, 2005, 45 (02) :233-244
[33]   Modulation of Ca2+ channels by G-protein beta gamma subunits [J].
Herlitze, S ;
Garcia, DE ;
Mackie, K ;
Hille, B ;
Scheuer, T ;
Catterall, WA .
NATURE, 1996, 380 (6571) :258-262
[34]   Channelopathies in idiopathic epilepsy [J].
Heron, Sarah E. ;
Scheffer, Ingrid E. ;
Berkovic, Samuel F. ;
Dibbens, Leanne M. ;
Mulley, John C. .
NEUROTHERAPEUTICS, 2007, 4 (02) :295-304
[35]   Regulation of back-propagating action potentials in hippocampal neurons [J].
Johnston, D ;
Hoffman, DA ;
Colbert, CM ;
Magee, JC .
CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (03) :288-292
[36]  
Jung HY, 1997, J NEUROSCI, V17, P6639
[37]   Reduced sodium current in Purkinje neurons from NaV1.1 mutant mice:: Implications for ataxia in severe myoclonic epilepsy in infancy [J].
Kalume, Franck ;
Yu, Frank H. ;
Westenbroek, Ruth E. ;
Scheuer, Todd ;
Catterall, William A. .
JOURNAL OF NEUROSCIENCE, 2007, 27 (41) :11065-11074
[38]   Molecular and cellular mechanisms of cardiac arrhythmias [J].
Keating, MT ;
Sanguinetti, MC .
CELL, 2001, 104 (04) :569-580
[39]   Impaired motor function in mice with cell-specific knockout of sodium channel Scn8a (NaV1.6) in cerebellar Purkinje neurons and granule cells [J].
Levin, Stephen I. ;
Khaliq, Zayd M. ;
Aman, Teresa K. ;
Grieco, Tina M. ;
Kearney, Jennifer A. ;
Raman, Indira M. ;
Meisler, Miriam H. .
JOURNAL OF NEUROPHYSIOLOGY, 2006, 96 (02) :785-793
[40]   FUNCTIONAL MODULATION OF BRAIN SODIUM-CHANNELS BY CAMP-DEPENDENT PHOSPHORYLATION [J].
LI, M ;
WEST, JW ;
LAI, Y ;
SCHEUER, T ;
CATTERALL, WA .
NEURON, 1992, 8 (06) :1151-1159