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Identifying local and descending inputs for primary sensory neurons
Yi Zhang, … , Xiang Zhou, Fan Wang
Yi Zhang, … , Xiang Zhou, Fan Wang
Published August 31, 2015
Citation Information: J Clin Invest. 2015;125(10):3782-3794. https://doi.org/10.1172/JCI81156.
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Research Article Neuroscience

Identifying local and descending inputs for primary sensory neurons

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Abstract

Primary pain and touch sensory neurons not only detect internal and external sensory stimuli, but also receive inputs from other neurons. However, the neuronal derived inputs for primary neurons have not been systematically identified. Using a monosynaptic rabies viruses–based transneuronal tracing method combined with sensory-specific Cre-drivers, we found that sensory neurons receive intraganglion, intraspinal, and supraspinal inputs, the latter of which are mainly derived from the rostroventral medulla (RVM). The viral-traced central neurons were largely inhibitory but also consisted of some glutamatergic neurons in the spinal cord and serotonergic neurons in the RVM. The majority of RVM-derived descending inputs were dual GABAergic and enkephalinergic (opioidergic). These inputs projected through the dorsolateral funiculus and primarily innervated layers I, II, and V of the dorsal horn, where pain-sensory afferents terminate. Silencing or activation of the dual GABA/enkephalinergic RVM neurons in adult animals substantially increased or decreased behavioral sensitivity, respectively, to heat and mechanical stimuli. These results are consistent with the fact that both GABA and enkephalin can exert presynaptic inhibition of the sensory afferents. Taken together, this work provides a systematic view of and a set of tools for examining peri- and extrasynaptic regulations of pain-afferent transmission.

Authors

Yi Zhang, Shengli Zhao, Erica Rodriguez, Jun Takatoh, Bao-Xia Han, Xiang Zhou, Fan Wang

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Figure 5

RVM-pre neurons project axons to dorsal spinal cord, and their activation evokes DRPs.

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RVM-pre neurons project axons to dorsal spinal cord, and their activatio...
(A) Representative images of labeled RVM neurons from mice coinjected with Lenti-Penk1-Cre and AAV-FLEX-GFP. (B and C) In situ hybridization showed that RVM neurons labeled by coinjection of Lenti-Penk1-Cre and AAV-FLEX-GFP express PENK1 (B) and/or GAD2 (C). (D–F) Costaining with anti-vGlut1 (marker for touch afferents) revealed that labeled RVM axons are concentrated in 2 regions (arrows): a superficial region above the vGlut1+ layers and the deep vGlut1+ lamina V. (G–I) Costaining with IB4 (marker of lamina II) revealed that labeled RVM axons innervate both lamina I and II. (J) Representative image of ChR2 expression in RVM neurons after coinjection of Lenti-Penk1-Cre and AAV-FLEX-hChR2-eYFP in RVM. (K and L) Optogenetic stimulation of ChR2-expressing axons in spinal block–evoked DRPs. Two representative traces are shown. (M and N) Light-evoked EPSP peak amplitude and latency were shown (n = 4 mice). Scale bar is 100 μm for all images.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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