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c-Maf-positive spinal cord neurons are critical elements of a dorsal horn circuit for mechanical hypersensitivity in neuropathy
Corticospinal tract (CST) neurons innervate the deep spinal dorsal horn to sustain chronic neuropathic pain. The majority of neurons targeted by the CST are interneurons expressing the transcription factor c-Maf. Here, we used intersectional genetics to decipher the function of these neurons in dors...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157139/ https://www.ncbi.nlm.nih.gov/pubmed/36947543 http://dx.doi.org/10.1016/j.celrep.2023.112295 |
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author | Frezel, Noémie Ranucci, Matteo Foster, Edmund Wende, Hagen Pelczar, Pawel Mendes, Raquel Ganley, Robert P. Werynska, Karolina d’Aquin, Simon Beccarini, Camilla Birchmeier, Carmen Zeilhofer, Hanns Ulrich Wildner, Hendrik |
author_facet | Frezel, Noémie Ranucci, Matteo Foster, Edmund Wende, Hagen Pelczar, Pawel Mendes, Raquel Ganley, Robert P. Werynska, Karolina d’Aquin, Simon Beccarini, Camilla Birchmeier, Carmen Zeilhofer, Hanns Ulrich Wildner, Hendrik |
author_sort | Frezel, Noémie |
collection | PubMed |
description | Corticospinal tract (CST) neurons innervate the deep spinal dorsal horn to sustain chronic neuropathic pain. The majority of neurons targeted by the CST are interneurons expressing the transcription factor c-Maf. Here, we used intersectional genetics to decipher the function of these neurons in dorsal horn sensory circuits. We find that excitatory c-Maf (c-Maf(EX)) neurons receive sensory input mainly from myelinated fibers and target deep dorsal horn parabrachial projection neurons and superficial dorsal horn neurons, thereby connecting non-nociceptive input to nociceptive output structures. Silencing c-Maf(EX) neurons has little effect in healthy mice but alleviates mechanical hypersensitivity in neuropathic mice. c-Maf(EX) neurons also receive input from inhibitory c-Maf and parvalbumin neurons, and compromising inhibition by these neurons caused mechanical hypersensitivity and spontaneous aversive behaviors reminiscent of c-Maf(EX) neuron activation. Our study identifies c-Maf(EX) neurons as normally silent second-order nociceptors that become engaged in pathological pain signaling upon loss of inhibitory control. |
format | Online Article Text |
id | pubmed-10157139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101571392023-05-05 c-Maf-positive spinal cord neurons are critical elements of a dorsal horn circuit for mechanical hypersensitivity in neuropathy Frezel, Noémie Ranucci, Matteo Foster, Edmund Wende, Hagen Pelczar, Pawel Mendes, Raquel Ganley, Robert P. Werynska, Karolina d’Aquin, Simon Beccarini, Camilla Birchmeier, Carmen Zeilhofer, Hanns Ulrich Wildner, Hendrik Cell Rep Article Corticospinal tract (CST) neurons innervate the deep spinal dorsal horn to sustain chronic neuropathic pain. The majority of neurons targeted by the CST are interneurons expressing the transcription factor c-Maf. Here, we used intersectional genetics to decipher the function of these neurons in dorsal horn sensory circuits. We find that excitatory c-Maf (c-Maf(EX)) neurons receive sensory input mainly from myelinated fibers and target deep dorsal horn parabrachial projection neurons and superficial dorsal horn neurons, thereby connecting non-nociceptive input to nociceptive output structures. Silencing c-Maf(EX) neurons has little effect in healthy mice but alleviates mechanical hypersensitivity in neuropathic mice. c-Maf(EX) neurons also receive input from inhibitory c-Maf and parvalbumin neurons, and compromising inhibition by these neurons caused mechanical hypersensitivity and spontaneous aversive behaviors reminiscent of c-Maf(EX) neuron activation. Our study identifies c-Maf(EX) neurons as normally silent second-order nociceptors that become engaged in pathological pain signaling upon loss of inhibitory control. Cell Press 2023-03-21 /pmc/articles/PMC10157139/ /pubmed/36947543 http://dx.doi.org/10.1016/j.celrep.2023.112295 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Frezel, Noémie Ranucci, Matteo Foster, Edmund Wende, Hagen Pelczar, Pawel Mendes, Raquel Ganley, Robert P. Werynska, Karolina d’Aquin, Simon Beccarini, Camilla Birchmeier, Carmen Zeilhofer, Hanns Ulrich Wildner, Hendrik c-Maf-positive spinal cord neurons are critical elements of a dorsal horn circuit for mechanical hypersensitivity in neuropathy |
title | c-Maf-positive spinal cord neurons are critical elements of a dorsal horn circuit for mechanical hypersensitivity in neuropathy |
title_full | c-Maf-positive spinal cord neurons are critical elements of a dorsal horn circuit for mechanical hypersensitivity in neuropathy |
title_fullStr | c-Maf-positive spinal cord neurons are critical elements of a dorsal horn circuit for mechanical hypersensitivity in neuropathy |
title_full_unstemmed | c-Maf-positive spinal cord neurons are critical elements of a dorsal horn circuit for mechanical hypersensitivity in neuropathy |
title_short | c-Maf-positive spinal cord neurons are critical elements of a dorsal horn circuit for mechanical hypersensitivity in neuropathy |
title_sort | c-maf-positive spinal cord neurons are critical elements of a dorsal horn circuit for mechanical hypersensitivity in neuropathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157139/ https://www.ncbi.nlm.nih.gov/pubmed/36947543 http://dx.doi.org/10.1016/j.celrep.2023.112295 |
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