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Nocistatin sensitizes TRPA1 channels in peripheral sensory neurons

机译:诺西他汀致敏外周感觉神经元中的TRPA1通道

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摘要

The ability of sensory neurons to detect potentially harmful stimuli relies on specialized molecular signal detectors such as transient receptor potential (TRP) A1 ion channels. TRPA1 is critically implicated in vertebrate nociception and different pain states. Furthermore, TRPA1 channels are subject to extensive modulation and regulation - processes which consequently affect nociceptive signaling. Here we show that the neuropeptide Nocistatin sensitizes TRPA1-dependent calcium influx upon application of the TRPA1 agonist mustard oil (MO) in cultured sensory neurons of dorsal root ganglia (DRG). Interestingly, TRPV1-mediated cellular calcium responses are unaffected by Nocistatin. Furthermore, Nocistatin-induced TRPA1-sensitization is likely independent of the Nocistatin binding partner 4-Nitrophenylphosphatase domain and non-neuronal SNAP25-like protein homolog 1 (NIPSNAP1) as assessed by siRNA-mediated knockdown in DRG cultures. In conclusion, we uncovered the sensitization of TRPA1 by Nocistatin, which may represent a novel mechanism how Nocistatin can modulate pain.
机译:感觉神经元检测潜在有害刺激物的能力取决于专门的分子信号检测器,例如瞬时受体电势(TRP)A1离子通道。 TRPA1与脊椎动物的伤害感受和不同的疼痛状态密切相关。此外,TRPA1通道需要进行广泛的调制和调节,因此会影响伤害性信号传导。在这里,我们显示神经肽Nocistatin可以在培养的背根神经节(DRG)感觉神经元中应用TRPA1激动剂芥末油(MO)时,使TRPA1依赖性钙离子增敏。有趣的是,TRPV1介导的细胞钙反应不受诺西他汀的影响。此外,如通过siRNA介导的DRG培养敲除评估的那样,诺西他汀诱导的TRPA1致敏可能独立于诺西他汀结合伴侣4-硝基苯基磷酸酶结构域和非神经元SNAP25样蛋白同源物1(NIPSNAP1)。总之,我们发现了Nocistatin对TRPA1的致敏作用,这可能代表了Nocistatin如何调节疼痛的新机制。

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