Calcium-sensing mechanism in TRPC5 channels contributing to retardation of neurite outgrowth

被引:85
作者
Hui, H
McHugh, D
Hannan, M
Zeng, FN
Xu, SZ
Khan, SUH
Levenson, R
Beech, DJ
Weiss, JL
机构
[1] Univ Leeds, Inst Membrane & Syst Biol, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Sheffield, Sheffield S10 2TN, S Yorkshire, England
[3] Penn State Coll Med, Dept Pharmacol, Hershey, PA 17033 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2006年 / 572卷 / 01期
基金
英国惠康基金;
关键词
D O I
10.1113/jphysiol.2005.102889
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The calcium- and sodium-permeable transient receptor potential channel TRPC5 has an inhibitory role in neuronal outgrowth but the mechanisms governing its activity are poorly understood. Here we propose a mechanism involving the neuronal calcium sensor-1 (NCS-1) protein. Inhibitory mutants of TRPC5 and NCS-1 enhance neurite outgrowth similarly. Mutant NCS-1 does not inhibit surface-expression of TRPC5 but generally suppresses channel activity, irrespective of whether it is evoked by carbachol, store depletion, lanthanides or elevated intracellular calcium. NCS-1 and TRPC5 are in the same protein complex in rat brain and NCS-1 directly binds to the TRPC5 C-terminus. The data suggest protein-protein interaction between NCS-1 and TRPC5, and involvement of this protein complex in retardation of neurite outgrowth.
引用
收藏
页码:165 / 172
页数:8
相关论文
共 31 条
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Zeng, FN ;
Xu, SZ ;
Jackson, PK ;
McHugh, D ;
Kumar, B ;
Fountain, SJ ;
Beech, DJ .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 559 (03) :739-750