Mi H, Deerinck T J, Jones M, Ellisman M H, Schwarz T L
Department of Molecular and Cellular Physiology, Beckman Center, Stanford University Medical Center, California 94305, USA.
J Neurosci. 1996 Apr 15;16(8):2421-9. doi: 10.1523/JNEUROSCI.16-08-02421.1996.
The presence of K+ channels on the Schwann cell plasma membrane suggests that Schwann cells may participate actively during action potential propagation in the peripheral nervous system. One such role for Schwann cells may be to maintain a constant extracellular concentration of K+ in the face of K+ efflux from a repolarizing axon. This buffering is likely to involve the influx of K+ through inward rectifying K+ channels. The molecular cloning of these genes allowed us to examine their expression and localization in Schwann cells in detail. In this study, we demonstrate the expression of two inward rectifying K+ channels, IRK1 and IRK3, in adult rat sciatic nerve. Immunocytochemistry using a polyclonal antibody against these proteins showed that the channels were highly localized at nodes in sciatic nerve. By immunoelectron microscopy, the nodal staining was shown to be concentrated in the microvilli of Schwann cells (also called nodal processes). The large surface area of the microvilli and their presence in the nodal space suggest involvement with ionic buffering. Thus, IRK1 and IRK3 are well suited to K+ buffering by virtue of both their biophysical properties and their localization. The restricted distribution of the inward rectifying K+ channels also provides an example of the highly regulated localization of ion channels to their specialized membrane domains. In the Schwann cell, where the nodal processes are a minute fraction of the total cell membrane, a potent mechanism must be present to concentrate the channels in this structure.
施万细胞质膜上存在钾离子通道,这表明施万细胞可能在周围神经系统动作电位的传播过程中发挥积极作用。施万细胞的一个可能作用是,在轴突复极化导致钾离子外流的情况下,维持细胞外钾离子浓度的恒定。这种缓冲作用可能涉及钾离子通过内向整流钾离子通道流入细胞。这些基因的分子克隆使我们能够详细研究它们在施万细胞中的表达和定位。在本研究中,我们证明了成年大鼠坐骨神经中两种内向整流钾离子通道IRK1和IRK3的表达。使用针对这些蛋白质的多克隆抗体进行免疫细胞化学分析表明,这些通道高度定位于坐骨神经的结处。通过免疫电子显微镜观察,结处的染色显示集中在施万细胞的微绒毛(也称为结突)中。微绒毛的大表面积及其在结间隙中的存在表明其与离子缓冲有关。因此,IRK1和IRK3凭借其生物物理特性和定位,非常适合进行钾离子缓冲。内向整流钾离子通道的分布受限也提供了一个例子,说明离子通道高度受调控地定位于其特定的膜结构域。在施万细胞中,结突仅占整个细胞膜的极小部分,因此必须存在一种有效机制,使通道集中在这个结构中。