Ganley Robert P, Iwagaki Noboru, del Rio Patricia, Baseer Najma, Dickie Allen C, Boyle Kieran A, Polgár Erika, Watanabe Masahiko, Abraira Victoria E, Zimmerman Amanda, Riddell John S, Todd Andrew J
Spinal Cord Group, Institute of Neuroscience and Psychology, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
Department of Anatomy, Hokkaido University School of Medicine, Sapporo 060-8638, Japan, and.
J Neurosci. 2015 May 13;35(19):7626-42. doi: 10.1523/JNEUROSCI.0406-15.2015.
The superficial dorsal horn of the spinal cord contains numerous inhibitory interneurons, which regulate the transmission of information perceived as touch, pain, or itch. Despite the importance of these cells, our understanding of their roles in the neuronal circuitry is limited by the difficulty in identifying functional populations. One group that has been identified and characterized consists of cells in the mouse that express green fluorescent protein (GFP) under control of the prion protein (PrP) promoter. Previous reports suggested that PrP-GFP cells belonged to a single morphological class (central cells), received inputs exclusively from unmyelinated primary afferents, and had axons that remained in lamina II. However, we recently reported that the PrP-GFP cells expressed neuronal nitric oxide synthase (nNOS) and/or galanin, and it has been shown that nNOS-expressing cells are more diverse in their morphology and synaptic connections. We therefore used a combined electrophysiological, pharmacological, and anatomical approach to reexamine the PrP-GFP cells. We provide evidence that they are morphologically diverse (corresponding to "unclassified" cells) and receive synaptic input from a variety of primary afferents, with convergence onto individual cells. We also show that their axons project into adjacent laminae and that they target putative projection neurons in lamina I. This indicates that the neuronal circuitry involving PrP-GFP cells is more complex than previously recognized, and suggests that they are likely to have several distinct roles in regulating the flow of somatosensory information through the dorsal horn.
脊髓浅表背角包含众多抑制性中间神经元,它们调节被感知为触觉、疼痛或瘙痒的信息传递。尽管这些细胞很重要,但我们对它们在神经回路中作用的理解因难以识别功能群体而受到限制。已被识别和表征的一组细胞是小鼠中在朊病毒蛋白(PrP)启动子控制下表达绿色荧光蛋白(GFP)的细胞。先前的报告表明,PrP-GFP细胞属于单一形态类别(中央细胞),仅从未髓鞘初级传入神经接收输入,并且其轴突保留在板层II中。然而,我们最近报告说,PrP-GFP细胞表达神经元型一氧化氮合酶(nNOS)和/或甘丙肽,并且已经表明,表达nNOS的细胞在形态和突触连接上更加多样化。因此,我们使用电生理、药理学和解剖学相结合的方法重新检查PrP-GFP细胞。我们提供的证据表明,它们在形态上是多样的(对应于“未分类”细胞),并从各种初级传入神经接收突触输入,且汇聚到单个细胞上。我们还表明,它们的轴突投射到相邻板层,并且它们靶向板层I中的假定投射神经元。这表明涉及PrP-GFP细胞的神经回路比以前认识的更复杂,并表明它们可能在调节通过背角的体感信息流中具有几个不同的作用。