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
[1]   A NEUTRAL AMINO-ACID CHANGE IN SEGMENT-IIS4 DRAMATICALLY ALTERS THE GATING PROPERTIES OF THE VOLTAGE-DEPENDENT SODIUM-CHANNEL [J].
AULD, VJ ;
GOLDIN, AL ;
KRAFTE, DS ;
CATTERALL, WA ;
LESTER, HA ;
DAVIDSON, N ;
DUNN, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :323-327
[2]   Inherited sodium channelopathies: Novel therapeutic and proarrhythmic molecular mechanisms [J].
Balser, JR .
TRENDS IN CARDIOVASCULAR MEDICINE, 2001, 11 (06) :229-237
[3]   Compact myelin dictates the differential targeting of two sodium channel isoforms in the same axon [J].
Boiko, T ;
Rasband, MN ;
Levinson, SR ;
Caldwell, JH ;
Mandel, G ;
Trimmer, JS ;
Matthews, G .
NEURON, 2001, 30 (01) :91-104
[4]   Molecular cloning, distribution and functional analysis of the NAV1.6.: Voltage-gated sodium channel from human brain [J].
Burbidge, SA ;
Dale, TJ ;
Powell, AJ ;
Whitaker, WRJ ;
Xie, XM ;
Romanos, MA ;
Clare, JJ .
MOLECULAR BRAIN RESEARCH, 2002, 103 (1-2) :80-90
[5]   MUTATION OF A NEW SODIUM-CHANNEL GENE, SCN8A, IN THE MOUSE MUTANT MOTOR END-PLATE DISEASE [J].
BURGESS, DL ;
KOHRMAN, DC ;
GALT, J ;
PLUMMER, NW ;
JONES, JM ;
SPEAR, B ;
MEISLER, MH .
NATURE GENETICS, 1995, 10 (04) :461-465
[6]   Sodium channel Nav1.6 is localized at nodes of Ranvier, dendrites, and synapses [J].
Caldwell, JH ;
Schaller, KL ;
Lasher, RS ;
Peles, E ;
Levinson, SR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) :5616-5620
[7]  
Cantrell AR, 1999, J NEUROSCI, V19, P5301
[8]  
Cantrell AR, 1997, J NEUROSCI, V17, P7330
[9]   Molecular mechanism of convergent regulation of brain Na+ channels by protein kinase C and protein kinase A anchored to AKAP-15 [J].
Cantrell, AR ;
Tibbs, VC ;
Yu, FH ;
Murphy, BJ ;
Sharp, EM ;
Qu, YS ;
Catterall, WA ;
Scheuer, T .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2002, 21 (01) :63-80
[10]   Neuromodulation of Na+ channels:: An unexpected form of cellular plasticity [J].
Cantrell, AR ;
Catterall, WA .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (06) :397-407