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A highly polarized excitable cell separates sodium channels from sodium-activated potassium channels by more than a millimeter

机译:高度极化的可激发细胞将钠通道与钠活化钾通道分开超过一毫米

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摘要

The bioelectrical properties and resulting metabolic demands of electrogenic cells are determined by their morphology and the subcellular localization of ion channels. The electric organ cells (electrocytes) of the electric fish Eigenmannia virescens generate action potentials (APs) with Na+ currents >10 μA and repolarize the AP with Na+-activated K+ (KNa) channels. To better understand the role of morphology and ion channel localization in determining the metabolic cost of electrocyte APs, we used two-photon three-dimensional imaging to determine the fine cellular morphology and immunohistochemistry to localize the electrocytes' ion channels, ionotropic receptors, and Na+-K+-ATPases. We found that electrocytes are highly polarized cells ∼1.5 mm in anterior-posterior length and ∼0.6 mm in diameter, containing ∼30,000 nuclei along the cell periphery. The cell's innervated posterior region is deeply invaginated and vascularized with complex ultrastructural features, whereas the anterior region is relatively smooth. Cholinergic receptors and Na+ channels are restricted to the innervated posterior region, whereas inward rectifier K+ channels and the KNa channels that terminate the electrocyte AP are localized to the anterior region, separated by >1 mm from the only sources of Na+ influx. In other systems, submicrometer spatial coupling of Na+ and KNa channels is necessary for KNa channel activation. However, our computational simulations showed that KNa channels at a great distance from Na+ influx can still terminate the AP, suggesting that KNa channels can be activated by distant sources of Na+ influx and overturning a long-standing assumption that AP-generating ion channels are restricted to the electrocyte's posterior face.
机译:电细胞的生物电特性和由此产生的代谢需求取决于它们的形态和离子通道的亚细胞定位。鱼类电子本征曼氏沼虾的电器官细胞(细胞)产生Na + 电流> 10μA的动作电位(AP),并用Na + 激活的K使AP极化。 + (KNa)频道。为了更好地了解形态学和离子通道定位在确定细胞AP代谢成本中的作用,我们使用了两光子三维成像来确定精细的细胞形态学和免疫组织化学,以定位细胞的离子通道,离子型受体和Na + -K + -ATPases。我们发现,细胞是高度极化的细胞,前后长度约1.5 mm,直径约0.6 mm,沿细胞外围含有约30,000个核。细胞的神经支配后区深陷并具有复杂的超微结构特征,而前血管则相对光滑。胆碱能受体和Na + 通道仅限于神经支配的后部区域,而内向整流子K + 通道和终止细胞AP的KNa通道则位于前部区域,与唯一的Na + 流入源相隔> 1 mm。在其他系统中,Na + 与KNa通道的亚微米空间耦合对于激活KNa通道是必需的。但是,我们的计算模拟表明,距Na + 流入量很远的KNa通道仍可以终止AP,这表明KNa通道可以被Na + 的遥远源激活涌入并推翻了一个长期的假设,即产生AP的离子通道仅限于细胞的后表面。

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