Scheff N N, Yilmaz E, Gold M S
The Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, USA Department of Anesthesiology, University of Pittsburgh, Pittsburgh, PA, USA Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, PA, USA.
The Center for Neuroscience, University of Pittsburgh, Pittsburgh, PA, USA Department of Anesthesiology, University of Pittsburgh, Pittsburgh, PA, USA Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, PA, USA
J Physiol. 2014 Nov 15;592(22):4969-93. doi: 10.1113/jphysiol.2014.278036. Epub 2014 Sep 19.
The Na(+)-Ca(2+) exchanger (NCX) appears to play an important role in the regulation of the high K(+)-evoked Ca(2+) transient in putative nociceptive dorsal root ganglion (DRG) neurons. The purpose of the present study was to (1) characterize the properties of NCX activity in subpopulations of DRG neurons, (2) identify the isoform(s) underlying NCX activity, and (3) begin to assess the function of the isoform(s) in vivo. In retrogradely labelled neurons from the glabrous skin of adult male Sprague-Dawley rats, NCX activity, as assessed with fura-2-based microfluorimetry, was only detected in putative nociceptive IB4+ neurons. There were two modes of NCX activity: one was evoked in response to relatively large and long lasting (∼325 nm for >12 s) increases in the concentration of intracellular Ca(2+) ([Ca(2+)]i), and a second was active at resting [Ca(2+)]i > ∼150 nm. There also were two modes of evoked activity: one that decayed relatively rapidly (<5 min) and a second that persisted (>10 min). Whereas mRNA encoding all three NCX isoforms (NCX1-3) was detected in putative nociceptive cutaneous neurons with single cell PCR, pharmacological analysis and small interfering RNA (siRNA) knockdown of each isoform in vivo suggested that NCX2 and 3 were responsible for NCX activity. Western blot analyses suggested that NCX isoforms were differentially distributed within sensory neurons. Functional assays of excitability, action potential propagation, and nociceptive behaviour suggest NCX activity has little influence on excitability per se, but instead influences axonal conduction velocity, resting membrane potential, and nociceptive threshold. Together these results indicate that the function of NCX in the regulation of [Ca(2+)]i in putative nociceptive neurons may be unique relative to other cells in which these exchanger isoforms have been characterized and it has the potential to influence sensory neuron properties at multiple levels.
钠钙交换体(NCX)似乎在调节假定的伤害性背根神经节(DRG)神经元中高钾诱发的钙瞬变方面发挥重要作用。本研究的目的是:(1)描述DRG神经元亚群中NCX活性的特性;(2)确定构成NCX活性的亚型;(3)开始评估该亚型在体内的功能。在用基于fura-2的显微荧光测定法评估的成年雄性Sprague-Dawley大鼠无毛皮肤逆行标记神经元中,仅在假定的伤害性IB4+神经元中检测到NCX活性。NCX活性有两种模式:一种是细胞内钙浓度([Ca(2+)]i)相对大幅且持续较长时间(>12秒时约为325纳米)升高时诱发的;另一种在静息[Ca(2+)]i>约150纳米时处于活跃状态。诱发活性也有两种模式:一种衰减相对较快(<5分钟),另一种持续存在(>10分钟)。虽然通过单细胞PCR在假定的伤害性皮肤神经元中检测到编码所有三种NCX亚型(NCX1 - 3)的mRNA,但体内对每种亚型的药理学分析和小干扰RNA(siRNA)敲低表明,NCX2和3负责NCX活性。蛋白质印迹分析表明,NCX亚型在感觉神经元内分布存在差异。兴奋性、动作电位传导和伤害性行为的功能测定表明,NCX活性本身对兴奋性影响很小,但会影响轴突传导速度、静息膜电位和伤害性阈值。这些结果共同表明,相对于已对这些交换体亚型进行表征的其他细胞,NCX在调节假定的伤害性神经元中[Ca(2+)]i的功能可能是独特的,并且它有可能在多个水平上影响感觉神经元特性。