Cargando…

Dermal macrophages set pain sensitivity by modulating the amount of tissue NGF through an SNX25–Nrf2 pathway

Cross-talk between peripheral neurons and immune cells is important in pain sensation. We identified Snx25 as a pain-modulating gene in a transgenic mouse line with reduced pain sensitivity. Conditional deletion of Snx25 in monocytes and macrophages, but not in peripheral sensory neurons, in mice (S...

Descripción completa

Detalles Bibliográficos
Autores principales: Tanaka, Tatsuhide, Okuda, Hiroaki, Isonishi, Ayami, Terada, Yuki, Kitabatake, Masahiro, Shinjo, Takeaki, Nishimura, Kazuya, Takemura, Shoko, Furue, Hidemasa, Ito, Toshihiro, Tatsumi, Kouko, Wanaka, Akio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977679/
https://www.ncbi.nlm.nih.gov/pubmed/36703006
http://dx.doi.org/10.1038/s41590-022-01418-5
_version_ 1784899348202520576
author Tanaka, Tatsuhide
Okuda, Hiroaki
Isonishi, Ayami
Terada, Yuki
Kitabatake, Masahiro
Shinjo, Takeaki
Nishimura, Kazuya
Takemura, Shoko
Furue, Hidemasa
Ito, Toshihiro
Tatsumi, Kouko
Wanaka, Akio
author_facet Tanaka, Tatsuhide
Okuda, Hiroaki
Isonishi, Ayami
Terada, Yuki
Kitabatake, Masahiro
Shinjo, Takeaki
Nishimura, Kazuya
Takemura, Shoko
Furue, Hidemasa
Ito, Toshihiro
Tatsumi, Kouko
Wanaka, Akio
author_sort Tanaka, Tatsuhide
collection PubMed
description Cross-talk between peripheral neurons and immune cells is important in pain sensation. We identified Snx25 as a pain-modulating gene in a transgenic mouse line with reduced pain sensitivity. Conditional deletion of Snx25 in monocytes and macrophages, but not in peripheral sensory neurons, in mice (Snx25(cKO) mice) reduced pain responses in both normal and neuropathic conditions. Bone marrow transplantation using Snx25(cKO) and wild-type mice indicated that macrophages modulated pain sensitivity. Expression of sorting nexin (SNX)25 in dermal macrophages enhanced expression of the neurotrophic factor NGF through the inhibition of ubiquitin-mediated degradation of Nrf2, a transcription factor that activates transcription of Ngf. As such, dermal macrophages set the threshold for pain sensitivity through the production and secretion of NGF into the dermis, and they may cooperate with dorsal root ganglion macrophages in pain perception.
format Online
Article
Text
id pubmed-9977679
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group US
record_format MEDLINE/PubMed
spelling pubmed-99776792023-03-03 Dermal macrophages set pain sensitivity by modulating the amount of tissue NGF through an SNX25–Nrf2 pathway Tanaka, Tatsuhide Okuda, Hiroaki Isonishi, Ayami Terada, Yuki Kitabatake, Masahiro Shinjo, Takeaki Nishimura, Kazuya Takemura, Shoko Furue, Hidemasa Ito, Toshihiro Tatsumi, Kouko Wanaka, Akio Nat Immunol Article Cross-talk between peripheral neurons and immune cells is important in pain sensation. We identified Snx25 as a pain-modulating gene in a transgenic mouse line with reduced pain sensitivity. Conditional deletion of Snx25 in monocytes and macrophages, but not in peripheral sensory neurons, in mice (Snx25(cKO) mice) reduced pain responses in both normal and neuropathic conditions. Bone marrow transplantation using Snx25(cKO) and wild-type mice indicated that macrophages modulated pain sensitivity. Expression of sorting nexin (SNX)25 in dermal macrophages enhanced expression of the neurotrophic factor NGF through the inhibition of ubiquitin-mediated degradation of Nrf2, a transcription factor that activates transcription of Ngf. As such, dermal macrophages set the threshold for pain sensitivity through the production and secretion of NGF into the dermis, and they may cooperate with dorsal root ganglion macrophages in pain perception. Nature Publishing Group US 2023-01-26 2023 /pmc/articles/PMC9977679/ /pubmed/36703006 http://dx.doi.org/10.1038/s41590-022-01418-5 Text en © The Author(s) 2023 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
Tanaka, Tatsuhide
Okuda, Hiroaki
Isonishi, Ayami
Terada, Yuki
Kitabatake, Masahiro
Shinjo, Takeaki
Nishimura, Kazuya
Takemura, Shoko
Furue, Hidemasa
Ito, Toshihiro
Tatsumi, Kouko
Wanaka, Akio
Dermal macrophages set pain sensitivity by modulating the amount of tissue NGF through an SNX25–Nrf2 pathway
title Dermal macrophages set pain sensitivity by modulating the amount of tissue NGF through an SNX25–Nrf2 pathway
title_full Dermal macrophages set pain sensitivity by modulating the amount of tissue NGF through an SNX25–Nrf2 pathway
title_fullStr Dermal macrophages set pain sensitivity by modulating the amount of tissue NGF through an SNX25–Nrf2 pathway
title_full_unstemmed Dermal macrophages set pain sensitivity by modulating the amount of tissue NGF through an SNX25–Nrf2 pathway
title_short Dermal macrophages set pain sensitivity by modulating the amount of tissue NGF through an SNX25–Nrf2 pathway
title_sort dermal macrophages set pain sensitivity by modulating the amount of tissue ngf through an snx25–nrf2 pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977679/
https://www.ncbi.nlm.nih.gov/pubmed/36703006
http://dx.doi.org/10.1038/s41590-022-01418-5
work_keys_str_mv AT tanakatatsuhide dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT okudahiroaki dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT isonishiayami dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT teradayuki dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT kitabatakemasahiro dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT shinjotakeaki dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT nishimurakazuya dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT takemurashoko dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT furuehidemasa dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT itotoshihiro dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT tatsumikouko dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway
AT wanakaakio dermalmacrophagessetpainsensitivitybymodulatingtheamountoftissuengfthroughansnx25nrf2pathway