Rush Anthony M, Dib-Hajj Sulayman D, Waxman Stephen G
Department of Neurology, Center for Neuroscience and Regeneration Research, Yale School of Medicine, LCI 707, 333 Cedar Street, New Haven, CT 06510, USA.
J Physiol. 2005 May 1;564(Pt 3):803-15. doi: 10.1113/jphysiol.2005.083089. Epub 2005 Mar 10.
Sodium channels Na(v)1.2 and Na(v)1.6 are both normally expressed along premyelinated and myelinated axons at different stages of maturation and are also expressed in a subset of demyelinated axons, where coexpression of Na(v)1.6 together with the Na(+)/Ca(2+) exchanger is associated with axonal injury. It has been difficult to distinguish the currents produced by Na(v)1.2 and Na(v)1.6 in native neurones, and previous studies have not compared these channels within neuronal expression systems. In this study, we have characterized and directly compared Na(v)1.2 and Na(v)1.6 in a mammalian neuronal cell background and demonstrate differences in their properties that may affect neuronal behaviour. The Na(v)1.2 channel displays more depolarized activation and availability properties that may permit conduction of action potentials, even with depolarization. However, Na(v)1.2 channels show a greater accumulation of inactivation at higher frequencies of stimulation (20-100 Hz) than Na(v)1.6 and thus are likely to generate lower frequencies of firing. Na(v)1.6 channels produce a larger persistent current that may play a role in triggering reverse Na(+)/Ca(2+) exchange, which can injure demyelinated axons where Na(v)1.6 and the Na(+)/Ca(2+) exchanger are colocalized, while selective expression of Na(v)1.2 may support action potential electrogenesis, at least at lower frequencies, while producing a smaller persistent current.
钠通道Na(v)1.2和Na(v)1.6在成熟的不同阶段通常沿无髓鞘和有髓鞘轴突表达,并且也在一部分脱髓鞘轴突中表达,其中Na(v)1.6与Na(+)/Ca(2+)交换体的共表达与轴突损伤相关。在天然神经元中很难区分由Na(v)1.2和Na(v)1.6产生的电流,并且先前的研究没有在神经元表达系统中比较这些通道。在本研究中,我们在哺乳动物神经元细胞背景中对Na(v)1.2和Na(v)1.6进行了表征并直接比较,证明了它们在特性上的差异可能会影响神经元行为。Na(v)1.2通道表现出更多的去极化激活和可用性特性,这可能允许动作电位的传导,即使在去极化情况下也是如此。然而,与Na(v)1.6相比,Na(v)1.2通道在更高的刺激频率(20 - 100 Hz)下显示出更大的失活积累,因此可能产生更低的放电频率。Na(v)1.6通道产生更大的持续电流,这可能在触发反向Na(+)/Ca(2+)交换中起作用,这会损伤Na(v)1.6和Na(+)/Ca(2+)交换体共定位的脱髓鞘轴突,而Na(v)1.2的选择性表达可能支持动作电位的电发生,至少在较低频率下如此,同时产生较小的持续电流。