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Localization of TRP Channels in Healthy Oral Mucosa from Human Donors

The oral cavity is exposed to a remarkable range of noxious and innocuous conditions, including temperature fluctuations, mechanical forces, inflammation, and environmental and endogenous chemicals. How such changes in the oral environment are sensed is not completely understood. Transient receptor...

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Autores principales: Moayedi, Yalda, Michlig, Stephanie, Park, Mark, Koch, Alia, Lumpkin, Ellen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797210/
https://www.ncbi.nlm.nih.gov/pubmed/36635242
http://dx.doi.org/10.1523/ENEURO.0328-21.2022
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author Moayedi, Yalda
Michlig, Stephanie
Park, Mark
Koch, Alia
Lumpkin, Ellen A.
author_facet Moayedi, Yalda
Michlig, Stephanie
Park, Mark
Koch, Alia
Lumpkin, Ellen A.
author_sort Moayedi, Yalda
collection PubMed
description The oral cavity is exposed to a remarkable range of noxious and innocuous conditions, including temperature fluctuations, mechanical forces, inflammation, and environmental and endogenous chemicals. How such changes in the oral environment are sensed is not completely understood. Transient receptor potential (TRP) ion channels are a diverse family of molecular receptors that are activated by chemicals, temperature changes, and tissue damage. In non-neuronal cells, TRP channels play roles in inflammation, tissue development, and maintenance. In somatosensory neurons, TRP channels mediate nociception, thermosensation, and chemosensation. To assess whether TRP channels might be involved in environmental sensing in the human oral cavity, we investigated their distribution in human tongue and hard palate biopsies. TRPV3 and TRPV4 were expressed in epithelial cells with inverse expression patterns where they likely contribute to epithelial development and integrity. TRPA1 immunoreactivity was present in fibroblasts, immune cells, and neuronal afferents, consistent with known roles of TRPA1 in sensory transduction and response to damage and inflammation. TRPM8 immunoreactivity was found in lamina propria and neuronal subpopulations including within the end bulbs of Krause, consistent with a role in thermal sensation. TRPV1 immunoreactivity was identified in intraepithelial nerve fibers and end bulbs of Krause, consistent with roles in nociception and thermosensation. TRPM8 and TRPV1 immunoreactivity in end bulbs of Krause suggest that these structures contain a variety of neuronal afferents, including those that mediate nociception, thermosensation, and mechanotransduction. Collectively, these studies support the role of TRP channels in oral environmental surveillance and response.
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spelling pubmed-97972102022-12-29 Localization of TRP Channels in Healthy Oral Mucosa from Human Donors Moayedi, Yalda Michlig, Stephanie Park, Mark Koch, Alia Lumpkin, Ellen A. eNeuro Research Article: New Research The oral cavity is exposed to a remarkable range of noxious and innocuous conditions, including temperature fluctuations, mechanical forces, inflammation, and environmental and endogenous chemicals. How such changes in the oral environment are sensed is not completely understood. Transient receptor potential (TRP) ion channels are a diverse family of molecular receptors that are activated by chemicals, temperature changes, and tissue damage. In non-neuronal cells, TRP channels play roles in inflammation, tissue development, and maintenance. In somatosensory neurons, TRP channels mediate nociception, thermosensation, and chemosensation. To assess whether TRP channels might be involved in environmental sensing in the human oral cavity, we investigated their distribution in human tongue and hard palate biopsies. TRPV3 and TRPV4 were expressed in epithelial cells with inverse expression patterns where they likely contribute to epithelial development and integrity. TRPA1 immunoreactivity was present in fibroblasts, immune cells, and neuronal afferents, consistent with known roles of TRPA1 in sensory transduction and response to damage and inflammation. TRPM8 immunoreactivity was found in lamina propria and neuronal subpopulations including within the end bulbs of Krause, consistent with a role in thermal sensation. TRPV1 immunoreactivity was identified in intraepithelial nerve fibers and end bulbs of Krause, consistent with roles in nociception and thermosensation. TRPM8 and TRPV1 immunoreactivity in end bulbs of Krause suggest that these structures contain a variety of neuronal afferents, including those that mediate nociception, thermosensation, and mechanotransduction. Collectively, these studies support the role of TRP channels in oral environmental surveillance and response. Society for Neuroscience 2022-12-21 /pmc/articles/PMC9797210/ /pubmed/36635242 http://dx.doi.org/10.1523/ENEURO.0328-21.2022 Text en Copyright © 2022 Moayedi et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: New Research
Moayedi, Yalda
Michlig, Stephanie
Park, Mark
Koch, Alia
Lumpkin, Ellen A.
Localization of TRP Channels in Healthy Oral Mucosa from Human Donors
title Localization of TRP Channels in Healthy Oral Mucosa from Human Donors
title_full Localization of TRP Channels in Healthy Oral Mucosa from Human Donors
title_fullStr Localization of TRP Channels in Healthy Oral Mucosa from Human Donors
title_full_unstemmed Localization of TRP Channels in Healthy Oral Mucosa from Human Donors
title_short Localization of TRP Channels in Healthy Oral Mucosa from Human Donors
title_sort localization of trp channels in healthy oral mucosa from human donors
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797210/
https://www.ncbi.nlm.nih.gov/pubmed/36635242
http://dx.doi.org/10.1523/ENEURO.0328-21.2022
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