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

机译:TRPC5通道中的钙传感机制有助于延缓神经突的生长

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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 intra-cellular 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.
机译:钙和钠可渗透的瞬时受体电位通道TRPC5在神经元生长中具有抑制作用,但对其活性的机制了解甚少。在这里,我们提出了一种涉及神经钙传感器1(NCS-1)蛋白的机制。 TRPC5和NCS-1的抑制性突变体可类似地增强神经突的生长。突变的NCS-1不会抑制TRPC5的表面表达,但通常会抑制通道活性,而不管其是由卡巴胆碱引起的,贮存耗竭,镧系元素还是细胞内钙升高。 NCS-1和TRPC5在大鼠脑中处于同一蛋白质复合物中,NCS-1直接与TRPC5 C末端结合。数据表明NCS-1和TRPC5之间存在蛋白质-蛋白质相互作用,并且该蛋白质复合物参与了神经突生长的延缓。

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