CK2 accumulation at the axon initial segment depends on sodium channel Nav1

被引:30
作者
Hien, Y. E. [1 ]
Montersino, A. [1 ]
Castets, F. [1 ]
Leterrier, C. [1 ]
Filhol, O. [2 ]
Vacher, H. [1 ]
Dargent, B. [1 ]
机构
[1] Aix Marseille Univ, CNRS, Ctr Rech Neurobiol & Neurophysiol Marseille, UMR 7286, F-13916 Marseille, France
[2] CEA Grenoble, INSERM U1036, Inst Rech Technol & Sci Vivant, F-38054 Grenoble, France
关键词
Protein kinase CK2; Nav1; Phosphorylation; Phosphospecific antibody; Dominant negative; Axon initial segment; PROTEIN-KINASE CK2; BINDING MOTIF; ANKYRIN-G; PHOSPHORYLATION; IDENTIFICATION; NA(V)1.6; SUBUNITS;
D O I
10.1016/j.febslet.2014.07.032
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
Accumulation of voltage-gated sodium channel Nav1 at the axon initial segment (AIS), results from a direct interaction with ankyrin G. This interaction is regulated in vitro by the protein kinase CK2, which is also highly enriched at the AIS. Here, using phosphospecific antibodies and inhibition/depletion approaches, we showed that Nav1 channels are phosphorylated in vivo in their ankyrin-binding motif. Moreover, we observed that CK2 accumulation at the AIS depends on expression of Nav1 channels, with which CK2 forms tight complexes. Thus, the CK2-Nav1 interaction is likely to initiate an important regulatory mechanism to finely control Nav1 phosphorylation and, consequently, neuronal excitability. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3403 / 3408
页数:6
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