Motagally Mohamed A, Lukewich Mark K, Chisholm Susan P, Neshat Shadia, Lomax Alan E
Department of Physiology, Queen's University, Kingston, Ontario, Canada.
J Physiol. 2009 Jun 1;587(Pt 11):2623-34. doi: 10.1113/jphysiol.2009.172312. Epub 2009 Apr 29.
Inflammation has profound effects on the innervation of affected tissues, including altered neuronal excitability and neurotransmitter release. As Ca(2+) influx through voltage-gated Ca(2+) channels (VGCCs) is a critical determinant of excitation-secretion coupling in nerve terminals, the aim of this study was to characterize the effect of overnight incubation in the inflammatory mediator tumour necrosis factor alpha (TNFalpha; 1 nM) on VGCCs in dissociated neurons from mouse superior mesenteric ganglia (SMG). Voltage-gated Ca(2+) currents (I(Ca)) were measured using the perforated patch clamp technique and the VGCC subtypes present in SMG neurons were estimated based on inhibition by selective VGCC blockers: omega-conotoxin GVIA (300 nM; N-type), nifedipine (10 microM; L-type), and omega-conotoxin MVIIC (300 nM; N-, P/Q-type). We used intracellular Ca(2+) imaging with Fura-2 AM to compare Ca(2+) influx during depolarizations in control and TNFalpha-treated neurons. TNF receptor and VGCC mRNA expression were measured using PCR, and channel alpha subunit (CaV2.2) was localized with immunohistochemistry. Incubation in TNFalpha significantly decreased I(Ca) amplitude and depolarization-induced Ca(2+) influx. The reduction in I(Ca) was limited to omega-conotoxin GVIA-sensitive N-type Ca(2+) channels. Depletion of glial cells by incubation in cytosine arabinoside (5 microM) did not affect I(Ca) inhibition by TNFalpha. Preincubation of neurons with SC-514 (20 microM) or BAY 11-7082 (1 microM), which both inhibit nuclear factor kappaB signalling, prevented the reduction in I(Ca) by TNFalpha. Inhibition of N-type VGCCs following TNFalpha incubation was associated with a decrease in CaV2.2 mRNA and reduced membrane localization of CaV2.2 immunoreactivity. These data suggest that TNFalpha inhibits I(Ca) in SMG neurons and identify a novel role for NF-kappaB in the regulation of neurotransmitter release during inflammatory conditions with elevated circulating TNFalpha, such as Crohn's disease and Guillain-Barré syndrome.
炎症对受影响组织的神经支配具有深远影响,包括改变神经元兴奋性和神经递质释放。由于通过电压门控钙通道(VGCCs)的Ca(2+)内流是神经末梢兴奋 - 分泌偶联的关键决定因素,本研究的目的是表征在炎性介质肿瘤坏死因子α(TNFα;1 nM)中过夜孵育对来自小鼠肠系膜上神经节(SMG)的解离神经元中VGCCs的影响。使用穿孔膜片钳技术测量电压门控钙电流(I(Ca)),并基于选择性VGCC阻滞剂的抑制作用估计SMG神经元中存在的VGCC亚型:ω-芋螺毒素GVIA(300 nM;N型)、硝苯地平(10 μM;L型)和ω-芋螺毒素MVIIC(300 nM;N -、P/Q型)。我们使用Fura - 2 AM进行细胞内钙成像,以比较对照神经元和TNFα处理神经元在去极化期间的Ca(2+)内流。使用PCR测量TNF受体和VGCC mRNA表达,并用免疫组织化学定位通道α亚基(CaV2.2)。在TNFα中孵育显著降低I(Ca)幅度和去极化诱导的Ca(2+)内流。I(Ca)的降低仅限于对ω-芋螺毒素GVIA敏感的N型钙通道。通过在阿糖胞苷(5 μM)中孵育使神经胶质细胞耗竭并不影响TNFα对I(Ca)的抑制作用。用SC - 514(20 μM)或BAY 11 - 7082(1 μM)对神经元进行预孵育可抑制核因子κB信号传导,从而防止TNFα导致的I(Ca)降低。TNFα孵育后对N型VGCCs的抑制与CaV2.2 mRNA减少和CaV2.2免疫反应性的膜定位降低有关。这些数据表明TNFα抑制SMG神经元中的I(Ca),并确定了NF - κB在循环TNFα升高的炎症状态(如克罗恩病和格林 - 巴利综合征)期间神经递质释放调节中的新作用。