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Pain sensing neurons promote tissue regeneration in adult mice

Tissue repair after injury in adult mammals, usually results in scarring and loss of function in contrast to lower vertebrates such as the newt and zebrafish that regenerate. Understanding the regulatory processes that guide the outcome of tissue repair is therefore a concerning challenge for regene...

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Autores principales: Rabiller, Lise, Labit, Elodie, Guissard, Christophe, Gilardi, Silveric, Guiard, Bruno P., Moulédous, Lionel, Silva, Marine, Mithieux, Gilles, Pénicaud, Luc, Lorsignol, Anne, Casteilla, Louis, Dromard, Cécile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516997/
https://www.ncbi.nlm.nih.gov/pubmed/34650070
http://dx.doi.org/10.1038/s41536-021-00175-7
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author Rabiller, Lise
Labit, Elodie
Guissard, Christophe
Gilardi, Silveric
Guiard, Bruno P.
Moulédous, Lionel
Silva, Marine
Mithieux, Gilles
Pénicaud, Luc
Lorsignol, Anne
Casteilla, Louis
Dromard, Cécile
author_facet Rabiller, Lise
Labit, Elodie
Guissard, Christophe
Gilardi, Silveric
Guiard, Bruno P.
Moulédous, Lionel
Silva, Marine
Mithieux, Gilles
Pénicaud, Luc
Lorsignol, Anne
Casteilla, Louis
Dromard, Cécile
author_sort Rabiller, Lise
collection PubMed
description Tissue repair after injury in adult mammals, usually results in scarring and loss of function in contrast to lower vertebrates such as the newt and zebrafish that regenerate. Understanding the regulatory processes that guide the outcome of tissue repair is therefore a concerning challenge for regenerative medicine. In multiple regenerative animal species, the nerve dependence of regeneration is well established, but the nature of the innervation required for tissue regeneration remains largely undefined. Using our model of induced adipose tissue regeneration in adult mice, we demonstrate here that nociceptive nerves promote regeneration and their removal impairs tissue regeneration. We also show that blocking the receptor for the nociceptive neuropeptide calcitonin gene-related peptide (CGRP) inhibits regeneration, whereas CGRP administration induces regeneration. These findings reveal that peptidergic nociceptive neurons are required for adult mice tissue regeneration.
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spelling pubmed-85169972021-10-29 Pain sensing neurons promote tissue regeneration in adult mice Rabiller, Lise Labit, Elodie Guissard, Christophe Gilardi, Silveric Guiard, Bruno P. Moulédous, Lionel Silva, Marine Mithieux, Gilles Pénicaud, Luc Lorsignol, Anne Casteilla, Louis Dromard, Cécile NPJ Regen Med Article Tissue repair after injury in adult mammals, usually results in scarring and loss of function in contrast to lower vertebrates such as the newt and zebrafish that regenerate. Understanding the regulatory processes that guide the outcome of tissue repair is therefore a concerning challenge for regenerative medicine. In multiple regenerative animal species, the nerve dependence of regeneration is well established, but the nature of the innervation required for tissue regeneration remains largely undefined. Using our model of induced adipose tissue regeneration in adult mice, we demonstrate here that nociceptive nerves promote regeneration and their removal impairs tissue regeneration. We also show that blocking the receptor for the nociceptive neuropeptide calcitonin gene-related peptide (CGRP) inhibits regeneration, whereas CGRP administration induces regeneration. These findings reveal that peptidergic nociceptive neurons are required for adult mice tissue regeneration. Nature Publishing Group UK 2021-10-14 /pmc/articles/PMC8516997/ /pubmed/34650070 http://dx.doi.org/10.1038/s41536-021-00175-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Rabiller, Lise
Labit, Elodie
Guissard, Christophe
Gilardi, Silveric
Guiard, Bruno P.
Moulédous, Lionel
Silva, Marine
Mithieux, Gilles
Pénicaud, Luc
Lorsignol, Anne
Casteilla, Louis
Dromard, Cécile
Pain sensing neurons promote tissue regeneration in adult mice
title Pain sensing neurons promote tissue regeneration in adult mice
title_full Pain sensing neurons promote tissue regeneration in adult mice
title_fullStr Pain sensing neurons promote tissue regeneration in adult mice
title_full_unstemmed Pain sensing neurons promote tissue regeneration in adult mice
title_short Pain sensing neurons promote tissue regeneration in adult mice
title_sort pain sensing neurons promote tissue regeneration in adult mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516997/
https://www.ncbi.nlm.nih.gov/pubmed/34650070
http://dx.doi.org/10.1038/s41536-021-00175-7
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