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Kv4 Channels Underlie the Subthreshold-Operating A-type K+-current in Nociceptive Dorsal Root Ganglion Neurons

机译:Kv4通道位于伤害性背根神经节神经元的阈下操作A型K +电流之下。

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摘要

The dorsal root ganglion (DRG) contains heterogeneous populations of sensory neurons including primary nociceptive neurons and C-fibers implicated in pain signaling. Recent studies have demonstrated DRG hyperexcitability associated with downregulation of A-type K+ channels; however, the molecular correlate of the corresponding A-type K+ current (IA) has remained hypothetical. Kv4 channels may underlie the IA in DRG neurons. We combined electrophysiology, molecular biology (Whole-Tissue and Single-Cell RT-PCR) and immunohistochemistry to investigate the molecular basis of the IA in acutely dissociated DRG neurons from 7- to 8-day-old rats. Whole-cell recordings demonstrate a robust tetraethylammonium-resistant (20 mM) and 4-aminopyridine-sensitive (5 mM) IA. Matching Kv4 channel properties, activation and inactivation of this IA occur in the subthreshold range of membrane potentials and the rate of recovery from inactivation is rapid and voltage-dependent. Among Kv4 transcripts, the DRG expresses significant levels of Kv4.1 and Kv4.3 mRNAs. Also, single small-medium diameter DRG neurons (∼30 μm) exhibit correlated frequent expression of mRNAs encoding Kv4.1 and Nav1.8, a known nociceptor marker. In contrast, the expressions of Kv1.4 and Kv4.2 mRNAs at the whole-tissue and single-cell levels are relatively low and infrequent. Kv4 protein expression in nociceptive DRG neurons was confirmed by immunohistochemistry, which demonstrates colocalization of Kv4.3 and Nav1.8, and negligible expression of Kv4.2. Furthermore, specific dominant-negative suppression and overexpression strategies confirmed the contribution of Kv4 channels to IA in DRG neurons. Contrasting the expression patterns of Kv4 channels in the central and peripheral nervous systems, we discuss possible functional roles of these channels in primary sensory neurons.
机译:背根神经节(DRG)包含感觉神经元的异质群体,包括与疼痛信号有关的初级伤害感受性神经元和C纤维。最近的研究表明,DRG过度兴奋与A型K +通道的下调有关。然而,相应的A型K +电流(IA)的分子相关性仍然是假设的。 Kv4通道可能是DRG神经元中IA的基础。我们结合电生理学,分子生物学(全组织和单细胞RT-PCR)和免疫组化研究了7至8天大的大鼠急性离解的DRG神经元中IA的分子基础。全细胞记录显示出强大的四乙基铵抗性(20 mM)和4-氨基吡啶敏感性(5 mM)IA。匹配Kv4通道特性,此IA的激活和失活发生在膜电位的亚阈值范围内,并且失活的恢复速率迅速且与电压有关。在Kv4转录本中,DRG表达显着水平的Kv4.1和Kv4.3 mRNA。此外,单个中小直径DRG神经元(约30μm)表现出相关的编码Kv4.1和Nav1.8(已知的伤害感受器标记)的mRNA的频繁表达。相反,在全组织和单细胞水平上Kv1.4和Kv4.2 mRNA的表达相对较低且很少见。免疫组化证实了伤害性DRG神经元中Kv4蛋白的表达,这表明Kv4.3和Nav1.8处于共定位,而Kv4.2的表达可忽略不计。此外,特定的显性负性抑制和过度表达策略证实了DRG神经元中Kv4通道对IA的贡献。对比中枢和外周神经系统中Kv4通道的表达模式,我们讨论了这些通道在初级感觉神经元中的可能功能作用。

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