TY - JOUR
T1 - Identification of Early RET+ Deep Dorsal Spinal Cord Interneurons in Gating Pain
AU - Cui, Lian
AU - Miao, Xuerong
AU - Liang, Lingli
AU - Abdus-Saboor, Ishmail
AU - Olson, William
AU - Fleming, Michael S.
AU - Ma, Minghong
AU - Tao, Yuan Xiang
AU - Luo, Wenqin
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/9/7
Y1 - 2016/9/7
N2 - The gate control theory (GCT) of pain proposes that pain- and touch-sensing neurons antagonize each other through spinal cord dorsal horn (DH) gating neurons. However, the exact neural circuits underlying the GCT remain largely elusive. Here, we identified a new population of deep layer DH (dDH) inhibitory interneurons that express the receptor tyrosine kinase Ret neonatally. These early RET+ dDH neurons receive excitatory as well as polysynaptic inhibitory inputs from touch- and/or pain-sensing afferents. In addition, they negatively regulate DH pain and touch pathways through both pre- and postsynaptic inhibition. Finally, specific ablation of early RET+ dDH neurons increases basal and chronic pain, whereas their acute activation reduces basal pain perception and relieves inflammatory and neuropathic pain. Taken together, our findings uncover a novel spinal circuit that mediates crosstalk between touch and pain pathways and suggest that some early RET+ dDH neurons could function as pain “gating” neurons.
AB - The gate control theory (GCT) of pain proposes that pain- and touch-sensing neurons antagonize each other through spinal cord dorsal horn (DH) gating neurons. However, the exact neural circuits underlying the GCT remain largely elusive. Here, we identified a new population of deep layer DH (dDH) inhibitory interneurons that express the receptor tyrosine kinase Ret neonatally. These early RET+ dDH neurons receive excitatory as well as polysynaptic inhibitory inputs from touch- and/or pain-sensing afferents. In addition, they negatively regulate DH pain and touch pathways through both pre- and postsynaptic inhibition. Finally, specific ablation of early RET+ dDH neurons increases basal and chronic pain, whereas their acute activation reduces basal pain perception and relieves inflammatory and neuropathic pain. Taken together, our findings uncover a novel spinal circuit that mediates crosstalk between touch and pain pathways and suggest that some early RET+ dDH neurons could function as pain “gating” neurons.
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U2 - 10.1016/j.neuron.2016.07.038
DO - 10.1016/j.neuron.2016.07.038
M3 - Article
C2 - 27545714
AN - SCOPUS:84995379913
SN - 0896-6273
VL - 91
SP - 1137
EP - 1153
JO - Neuron
JF - Neuron
IS - 5
ER -