Toledo-Aral J J, Moss B L, He Z J, Koszowski A G, Whisenand T, Levinson S R, Wolf J J, Silos-Santiago I, Halegoua S, Mandel G
Department of Neurobiology and Behavior, State University of New York at Stony Brook, 11794-5230, USA.
Proc Natl Acad Sci U S A. 1997 Feb 18;94(4):1527-32. doi: 10.1073/pnas.94.4.1527.
Membrane excitability in different tissues is due, in large part, to the selective expression of distinct genes encoding the voltage-dependent sodium channel. Although the predominant sodium channels in brain, skeletal muscle, and cardiac muscle have been identified, the major sodium channel types responsible for excitability within the peripheral nervous system have remained elusive. We now describe the deduced primary structure of a sodium channel, peripheral nerve type 1 (PN1), which is expressed at high levels throughout the peripheral nervous system and is targeted to nerve terminals of cultured dorsal root ganglion neurons. Studies using cultured PC12 cells indicate that both expression and targeting of PN1 is induced by treatment of the cells with nerve growth factor. The preferential localization suggests that the PN1 sodium channel plays a specific role in nerve excitability.
不同组织中的膜兴奋性在很大程度上归因于编码电压依赖性钠通道的不同基因的选择性表达。虽然已经确定了脑、骨骼肌和心肌中的主要钠通道,但负责外周神经系统兴奋性的主要钠通道类型仍然难以捉摸。我们现在描述一种钠通道——外周神经1型(PN1)的推导一级结构,它在整个外周神经系统中高水平表达,并靶向培养的背根神经节神经元的神经末梢。使用培养的PC12细胞进行的研究表明,用神经生长因子处理细胞可诱导PN1的表达和靶向。这种优先定位表明PN1钠通道在神经兴奋性中起特定作用。