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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2023
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.
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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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