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Background and tandem-pore potassium channels in magnocellular neurosecretory cells of the rat supraoptic nucleus

机译:大鼠视上核大细胞神经分泌细胞的背景和串联孔钾通道

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摘要

Magnocellular neurosecretory cells (MNCs) were isolated from the supraoptic nucleus of rat hypothalamus, and properties of K+ channels that may regulate the resting membrane potential and the excitability of MNCs were studied. MNCs showed large transient outward currents, typical of vasopressin- and oxytocin-releasing neurons. K+ channels in MNCs were identified by recording K+ channels that were open at rest in cell-attached and inside-out patches in symmetrical 150 mm KCl. Eight different K+ channels were identified and could be distinguished unambiguously by their single-channel kinetics and voltage-dependent rectification. Two K+ channels could be considered functional correlates of TASK-1 and TASK-3, as judged by their single-channel kinetics and high sensitivity to pHo. Three K+ channels showed properties similar to TREK-type tandem-pore K+ channels (TREK-1, TREK-2 and a novel TREK), as judged by their activation by membrane stretch, intracellular acidosis and arachidonic acid. One K+ channel was activated by application of pressure, arachidonic acid and alkaline pHi, and showed single-channel kinetics indistinguishable from those of TRAAK. One K+ channel showed strong inward rectification and single-channel conductance similar to those of a classical inward rectifier, IRK3. Finally, a K+ channel whose cloned counterpart has not yet been identified was highly sensitive to extracellular pH near the physiological range similar to those of TASK channels, and was the most active among all K+ channels. Our results show that in MNCs at rest, eight different types of K+ channels can be found and six of them belong to the tandem-pore K+ channel family. Various physiological and pathophysiological conditions may modulate these K+ channels and regulate the excitability of MNCs.
机译:从大鼠下丘脑的视上核中分离出了巨细胞神经分泌细胞(MNC),并研究了可调节静息膜电位和MNC兴奋性的K +通道的特性。 MNC显示出大的瞬时向外电流,这是释放加压素和催产素的神经元的典型现象。 MNC中的K +通道是通过在静态的150 mm KCl中记录静止且在细胞附着和由内而外的贴片中打开的K +通道来识别的。确定了八个不同的K +通道,可以通过它们的单通道动力学和电压依赖性整流来明确区分。根据其单通道动力学和对pHo的高敏感性判断,两个K +通道可被视为TASK-1和TASK-3的功能相关性。通过膜拉伸,细胞内酸中毒和花生四烯酸对它们的激活来判断,三个K +通道显示出与TREK型串联孔K +通道(TREK-1,TREK-2和新型TREK)相似的特性。通过施加压力,花生四烯酸和碱性pHi激活一个K +通道,并显示出与TRAAK难以区分的单通道动力学。一个K +通道显示出强大的内部整流和单通道电导,类似于经典的内部整流器IRK3。最后,尚未鉴定出克隆配对物的K +通道对生理范围附近的细胞外pH高度敏感,类似于TASK通道,并且在所有K +通道中最活跃。我们的结果表明,在静止的跨国公司中,可以找到八种不同类型的K +通道,其中六种属于串联孔K +通道家族。各种生理和病理生理条件可以调节这些K +通道并调节MNC的兴奋性。

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