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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...

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Autores principales: Warwick, Charles, Salsovic, Joseph, Hachisuka, Junichi, Smith, Kelly M., Sheahan, Tayler D., Chen, Haichao, Ibinson, James, Koerber, H. Richard, Ross, Sarah E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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