Molecular Genetics Unit, Laboratory of Sensory Biology, National Institute of Dental and Craniofacial Research/NIH, 49 Convent Drive, Bethesda, MD 20892, USA.
Science. 2013 May 24;340(6135):968-71. doi: 10.1126/science.1233765.
Itch is triggered by somatosensory neurons expressing the ion channel TRPV1 (transient receptor potential cation channel subfamily V member 1), but the mechanisms underlying this nociceptive response remain poorly understood. Here, we show that the neuropeptide natriuretic polypeptide b (Nppb) is expressed in a subset of TRPV1 neurons and found that Nppb(-/-) mice selectively lose almost all behavioral responses to itch-inducing agents. Nppb triggered potent scratching when injected intrathecally in wild-type and Nppb(-/-) mice, showing that this neuropeptide evokes itch when released from somatosensory neurons. Itch responses were blocked by toxin-mediated ablation of Nppb-receptor-expressing cells, but a second neuropeptide, gastrin-releasing peptide, still induced strong responses in the toxin-treated animals. Thus, our results define the primary pruriceptive neurons, characterize Nppb as an itch-selective neuropeptide, and reveal the next two stages of this dedicated neuronal pathway.
痒觉由表达离子通道 TRPV1(瞬时受体电位阳离子通道亚家族 V 成员 1)的躯体感觉神经元触发,但这种伤害性反应的机制仍知之甚少。在这里,我们表明,神经肽利尿钠肽 b(Nppb)在 TRPV1 神经元的一个亚群中表达,并且发现 Nppb(-/-) 小鼠选择性地失去了对所有致痒剂的几乎所有行为反应。Nppb 鞘内注射到野生型和 Nppb(-/-) 小鼠中会引发强烈的搔抓,表明这种神经肽从感觉神经元释放时会引发痒觉。用毒素介导的 Nppb 受体表达细胞消融阻断了瘙痒反应,但第二种神经肽,胃泌素释放肽,在毒素处理的动物中仍能引起强烈的反应。因此,我们的研究结果定义了主要的瘙痒神经元,将 Nppb 表征为一种瘙痒选择性神经肽,并揭示了这条专用神经元通路的接下来的两个阶段。