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Cell type-specific calcium imaging of central sensitization in mouse dorsal horn
Allodynia is a state in which pain is elicited by innocuous stimuli. Capsaicin applied to the skin results in an allodynia that extends to a broad region beyond the application site. This sensitization is thought to be mediated by spinal networks; however, we do not have a clear picture of which spi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440908/ https://www.ncbi.nlm.nih.gov/pubmed/36057681 http://dx.doi.org/10.1038/s41467-022-32608-2 |
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author | Warwick, Charles Salsovic, Joseph Hachisuka, Junichi Smith, Kelly M. Sheahan, Tayler D. Chen, Haichao Ibinson, James Koerber, H. Richard Ross, Sarah E. |
author_facet | Warwick, Charles Salsovic, Joseph Hachisuka, Junichi Smith, Kelly M. Sheahan, Tayler D. Chen, Haichao Ibinson, James Koerber, H. Richard Ross, Sarah E. |
author_sort | Warwick, Charles |
collection | PubMed |
description | Allodynia is a state in which pain is elicited by innocuous stimuli. Capsaicin applied to the skin results in an allodynia that extends to a broad region beyond the application site. This sensitization is thought to be mediated by spinal networks; however, we do not have a clear picture of which spinal neurons mediate this phenomenon. To address this gap, we used two-photon calcium imaging of excitatory interneurons and spinal projection neurons in the mouse spinal dorsal horn. To distinguish among neuronal subtypes, we developed CICADA, a cell profiling approach to identify cell types during calcium imaging. We then identified capsaicin-responsive and capsaicin-sensitized neuronal populations. Capsaicin-sensitized neurons showed emergent responses to innocuous input and increased receptive field sizes consistent with psychophysical reports. Finally, we identified spinal output neurons that showed enhanced responses from innocuous input. These experiments provide a population-level view of central sensitization and a framework with which to model somatosensory integration in the dorsal horn. |
format | Online Article Text |
id | pubmed-9440908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94409082022-09-05 Cell type-specific calcium imaging of central sensitization in mouse dorsal horn Warwick, Charles Salsovic, Joseph Hachisuka, Junichi Smith, Kelly M. Sheahan, Tayler D. Chen, Haichao Ibinson, James Koerber, H. Richard Ross, Sarah E. Nat Commun Article Allodynia is a state in which pain is elicited by innocuous stimuli. Capsaicin applied to the skin results in an allodynia that extends to a broad region beyond the application site. This sensitization is thought to be mediated by spinal networks; however, we do not have a clear picture of which spinal neurons mediate this phenomenon. To address this gap, we used two-photon calcium imaging of excitatory interneurons and spinal projection neurons in the mouse spinal dorsal horn. To distinguish among neuronal subtypes, we developed CICADA, a cell profiling approach to identify cell types during calcium imaging. We then identified capsaicin-responsive and capsaicin-sensitized neuronal populations. Capsaicin-sensitized neurons showed emergent responses to innocuous input and increased receptive field sizes consistent with psychophysical reports. Finally, we identified spinal output neurons that showed enhanced responses from innocuous input. These experiments provide a population-level view of central sensitization and a framework with which to model somatosensory integration in the dorsal horn. Nature Publishing Group UK 2022-09-03 /pmc/articles/PMC9440908/ /pubmed/36057681 http://dx.doi.org/10.1038/s41467-022-32608-2 Text en © The Author(s) 2022 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 Warwick, Charles Salsovic, Joseph Hachisuka, Junichi Smith, Kelly M. Sheahan, Tayler D. Chen, Haichao Ibinson, James Koerber, H. Richard Ross, Sarah E. Cell type-specific calcium imaging of central sensitization in mouse dorsal horn |
title | Cell type-specific calcium imaging of central sensitization in mouse dorsal horn |
title_full | Cell type-specific calcium imaging of central sensitization in mouse dorsal horn |
title_fullStr | Cell type-specific calcium imaging of central sensitization in mouse dorsal horn |
title_full_unstemmed | Cell type-specific calcium imaging of central sensitization in mouse dorsal horn |
title_short | Cell type-specific calcium imaging of central sensitization in mouse dorsal horn |
title_sort | cell type-specific calcium imaging of central sensitization in mouse dorsal horn |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440908/ https://www.ncbi.nlm.nih.gov/pubmed/36057681 http://dx.doi.org/10.1038/s41467-022-32608-2 |
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