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Specific distribution of sodium channels in axons of rat embryo spinal motoneurones

机译:大鼠胚胎脊髓运动神经元轴突中钠通道的特异性分布

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class="enumerated" style="list-style-type:decimal">The distribution of Na+ channels and development of excitability were investigated in vitro in purified spinal motoneurones obtained from rat embryos at E14, using electrophysiological, immunocytochemical and autoradiographical methods.One hour after plating the motoneurones (DIV0), only somas were present. They expressed a robust delayed rectifier K+ current (IDR) and a fast-inactivating A-type K+ current (IA). The rapid neuritic outgrowth was paralleled by the emergence of a fast-activating TTX-sensitive sodium current (INa), and by an increase in both K+ currents.The change in the three currents was measured daily, up to DIV8. The large increase in INa observed after DIV2 was accompanied by the onset of excitability. Spontaneous activity was observed as from DIV6.The occurrence of axonal differentiation was confirmed by the fact that (i) only one neurite per motoneurone generated antidromic action potentials; and (ii) 125I-α-scorpion toxin binding, a specific marker of Na+ channels, labelled only one neurite and the greatest density was observed in the initial segment. Na+ channels therefore selectively targeted the axon and were absent from the dendrites and somas.The specific distribution of Na+ channels was detectable as soon as the neurites began to grow. When the neuritic outgrowth was blocked by nocodazole, no INa developed.It was concluded that, in spinal embryonic motoneurone in cell culture, Na+ channels, the expression of which starts with neuritic differentiation, are selectively addressed to the axonal process, whereas K+ channels are present in the soma prior to the neuritic outgrowth.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 使用电生理,免疫细胞化学和放射自显影方法,在E14处从大鼠胚胎获得的纯化的脊髓运动神经元中,体外研究Na + 通道的分布和兴奋性的发展。 一小时后电镀运动神经元(DIV0),仅存在体细胞。他们表示了鲁棒的延迟整流器K + 电流(IDR)和快速失活的A型K + 电流(IA)。快速激活的TTX敏感钠电流(INa)的出现以及两个K + 电流的增加都与神经质的迅速生长并存。 每天测量三个电流,直到DIV8。 DIV2后观察到的INa大量增加伴随着兴奋性的发作。从DIV6开始观察到自发活性。 轴突分化的发生由以下事实证实:(i)每个运动神经元仅一个神经突产生抗皮肤动作电位; (ii) 125 I-α-蝎毒素结合,Na + 通道的特异性标记,仅标记一个神经突,并且在初始节段中观察到最大密度。因此,Na + 通道选择性地靶向轴突,而树突和体细胞中则没有。 Na + 通道的特定分布可在第一时间被检测到。神经突开始生长。结论当在诺考达唑阻滞神经生长时,没有形成INa。 结论是,在细胞培养的脊髓胚胎运动神经元中,Na + 通道的表达始于神经分化,选择性地针对轴突过程,而在神经长出之前,K + 通道存在于躯体中。

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