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Nuclear Factor I/A Controls A-fiber Nociceptor Development
Noxious mechanical information is transmitted through molecularly distinct nociceptors, with pinprick-evoked sharp sensitivity via A-fiber nociceptors marked by developmental expression of the neuropeptide Y receptor 2 (Npy2r) and von Frey filament-evoked punctate pressure information via unmyelinat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340684/ https://www.ncbi.nlm.nih.gov/pubmed/32221845 http://dx.doi.org/10.1007/s12264-020-00486-7 |
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author | Qi, Lu Yin, Guangjuan Zhang, Yongchao Tao, Yeqi Wu, Xiaohua Gronostajski, Richard M. Qiu, Mengsheng Liu, Yang |
author_facet | Qi, Lu Yin, Guangjuan Zhang, Yongchao Tao, Yeqi Wu, Xiaohua Gronostajski, Richard M. Qiu, Mengsheng Liu, Yang |
author_sort | Qi, Lu |
collection | PubMed |
description | Noxious mechanical information is transmitted through molecularly distinct nociceptors, with pinprick-evoked sharp sensitivity via A-fiber nociceptors marked by developmental expression of the neuropeptide Y receptor 2 (Npy2r) and von Frey filament-evoked punctate pressure information via unmyelinated C fiber nociceptors marked by MrgprD. However, the molecular programs controlling their development are only beginning to be understood. Here we demonstrate that Npy2r-expressing sensory neurons are in fact divided into two groups, based on transient or persistent Npy2r expression. Npy2r-transient neurons are myelinated, likely including A-fiber nociceptors, whereas Npy2r-persistent ones belong to unmyelinated pruriceptors that co-express Nppb. We then showed that the transcription factors NFIA and Runx1 are necessary for the development of Npy2r-transient A-fiber nociceptors and MrgprD(+) C-fiber nociceptors, respectively. Behaviorally, mice with conditional knockout of Nfia, but not Runx1 showed a marked attenuation of pinprick-evoked nocifensive responses. Our studies therefore identify a transcription factor controlling the development of myelinated nociceptors. |
format | Online Article Text |
id | pubmed-7340684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-73406842020-07-09 Nuclear Factor I/A Controls A-fiber Nociceptor Development Qi, Lu Yin, Guangjuan Zhang, Yongchao Tao, Yeqi Wu, Xiaohua Gronostajski, Richard M. Qiu, Mengsheng Liu, Yang Neurosci Bull Original Article Noxious mechanical information is transmitted through molecularly distinct nociceptors, with pinprick-evoked sharp sensitivity via A-fiber nociceptors marked by developmental expression of the neuropeptide Y receptor 2 (Npy2r) and von Frey filament-evoked punctate pressure information via unmyelinated C fiber nociceptors marked by MrgprD. However, the molecular programs controlling their development are only beginning to be understood. Here we demonstrate that Npy2r-expressing sensory neurons are in fact divided into two groups, based on transient or persistent Npy2r expression. Npy2r-transient neurons are myelinated, likely including A-fiber nociceptors, whereas Npy2r-persistent ones belong to unmyelinated pruriceptors that co-express Nppb. We then showed that the transcription factors NFIA and Runx1 are necessary for the development of Npy2r-transient A-fiber nociceptors and MrgprD(+) C-fiber nociceptors, respectively. Behaviorally, mice with conditional knockout of Nfia, but not Runx1 showed a marked attenuation of pinprick-evoked nocifensive responses. Our studies therefore identify a transcription factor controlling the development of myelinated nociceptors. Springer Singapore 2020-03-28 /pmc/articles/PMC7340684/ /pubmed/32221845 http://dx.doi.org/10.1007/s12264-020-00486-7 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Qi, Lu Yin, Guangjuan Zhang, Yongchao Tao, Yeqi Wu, Xiaohua Gronostajski, Richard M. Qiu, Mengsheng Liu, Yang Nuclear Factor I/A Controls A-fiber Nociceptor Development |
title | Nuclear Factor I/A Controls A-fiber Nociceptor Development |
title_full | Nuclear Factor I/A Controls A-fiber Nociceptor Development |
title_fullStr | Nuclear Factor I/A Controls A-fiber Nociceptor Development |
title_full_unstemmed | Nuclear Factor I/A Controls A-fiber Nociceptor Development |
title_short | Nuclear Factor I/A Controls A-fiber Nociceptor Development |
title_sort | nuclear factor i/a controls a-fiber nociceptor development |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340684/ https://www.ncbi.nlm.nih.gov/pubmed/32221845 http://dx.doi.org/10.1007/s12264-020-00486-7 |
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