Direct interaction with contactin targets voltage-gated sodium channel Nav1.9/NaN to the cell membrane.

被引:66
作者
Liu, CJ
Dib-Hajj, SD
Black, JA
Greenwood, J
Lian, Z
Waxman, SG
机构
[1] Yale Univ, Sch Med, Dept Neurol, Neurosci Res Ctr,, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Paralyzed Vet Amer,Eastern Paralysed Vet Assoc, Neurosci Res Ctr, New Haven, CT 06510 USA
[3] Transmol Inc, Birmingham, AL 35243 USA
[4] Vet Affairs Connecticut Healthcare Syst, West Haven, CT 06516 USA
[5] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06536 USA
关键词
D O I
10.1074/jbc.M108699200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mechanisms that target various sodium channels within different regions of the neuronal membrane, which they endow with different physiological properties, are not yet understood. To examine this issue we studied the voltage-gated sodium channel Na(v)1.9/NaN, which is preferentially expressed in small sensory neurons of dorsal root ganglia and trigeminal ganglia and the nonmyelinated axons that arise from them. Our results show that the cell adhesion molecule contactin binds directly to Na(v)1.9/NaN and recruits tenascin to the protein complex in vitro. Na(v)1.9/NaN and contactin coimmunoprecipitate from dorsal root ganglia and transfected Chinese hamster ovary cell line, and co-localize in the C-type neuron soma and along nonmyelinated C-fibers and at nerve endings in the skin. Co-transfection of Chinese hamster ovary cells with Na(v)1.9/NaN and contactin enhances the surface expression of the sodium channel over that of Na,1.9/NaN alone. Thus contactin binds directly to Na(v)1.9/NaN and participates in the surface localization of this channel along nonmyelinated axons.
引用
收藏
页码:46553 / 46561
页数:9
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