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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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. |
doi_str_mv | 10.1523/ENEURO.0328-21.2022 |
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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. 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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.</description><subject>Humans</subject><subject>Inflammation - metabolism</subject><subject>Mechanotransduction, Cellular</subject><subject>Mouth Mucosa - metabolism</subject><subject>New Research</subject><subject>Thermosensing - physiology</subject><subject>Transient Receptor Potential Channels - metabolism</subject><subject>TRPA1 Cation Channel - metabolism</subject><issn>2373-2822</issn><issn>2373-2822</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkdFLwzAQxoMobsz9BYLk0ZfO5JIm3YsgszphOhnbc0jT1FXaZDarMP96NzbHfLqD-77vjvshdE3JgMbA7tK3dDGbDgiDJAI6AAJwhrrAJIsgATg_6TuoH8InIYQKkDShl6jDhGAxcOiidOKNrsofvS69w77A89k7Hi21c7YKuHR4bHW1Xm7wtNEVfm2NDxoXja_xuK21w4_e-SZcoYtCV8H2D7WHFk_pfDSOJtPnl9HDJDIsERDlWZzFRuQJyXIBXGQUGKecFZbnmhR5UlhKDBiuubVS2qG2Qug4K4RhJuGC9dD9PnfVZrXNjXXr7Vlq1ZS1bjbK61L9n7hyqT78txrKoQRKtgG3h4DGf7U2rFVdBmOrSjvr26BAilhKRgjfStleahofQmOL4xpK1I6B2jNQOwYKqNox2LpuTi88ev4-zn4B7PKDDg</recordid><startdate>20221101</startdate><enddate>20221101</enddate><creator>Moayedi, Yalda</creator><creator>Michlig, Stephanie</creator><creator>Park, Mark</creator><creator>Koch, Alia</creator><creator>Lumpkin, Ellen A</creator><general>Society for Neuroscience</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0600-1253</orcidid></search><sort><creationdate>20221101</creationdate><title>Localization of TRP Channels in Healthy Oral Mucosa from Human Donors</title><author>Moayedi, Yalda ; Michlig, Stephanie ; Park, Mark ; Koch, Alia ; Lumpkin, Ellen A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3862-db5b5c6d80bd6246b1234143fe4da0fd8fe10c2c4a4ee77e9ae66a5bf6c3c8463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Humans</topic><topic>Inflammation - metabolism</topic><topic>Mechanotransduction, Cellular</topic><topic>Mouth Mucosa - metabolism</topic><topic>New Research</topic><topic>Thermosensing - physiology</topic><topic>Transient Receptor Potential Channels - metabolism</topic><topic>TRPA1 Cation Channel - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moayedi, Yalda</creatorcontrib><creatorcontrib>Michlig, Stephanie</creatorcontrib><creatorcontrib>Park, Mark</creatorcontrib><creatorcontrib>Koch, Alia</creatorcontrib><creatorcontrib>Lumpkin, Ellen A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>eNeuro</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moayedi, Yalda</au><au>Michlig, Stephanie</au><au>Park, Mark</au><au>Koch, Alia</au><au>Lumpkin, Ellen A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Localization of TRP Channels in Healthy Oral Mucosa from Human Donors</atitle><jtitle>eNeuro</jtitle><addtitle>eNeuro</addtitle><date>2022-11-01</date><risdate>2022</risdate><volume>9</volume><issue>6</issue><spage>ENEURO.0328-21.2022</spage><pages>ENEURO.0328-21.2022-</pages><issn>2373-2822</issn><eissn>2373-2822</eissn><abstract>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.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>36635242</pmid><doi>10.1523/ENEURO.0328-21.2022</doi><orcidid>https://orcid.org/0000-0002-0600-1253</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Humans Inflammation - metabolism Mechanotransduction, Cellular Mouth Mucosa - metabolism New Research Thermosensing - physiology Transient Receptor Potential Channels - metabolism TRPA1 Cation Channel - metabolism |
title | Localization of TRP Channels in Healthy Oral Mucosa from Human Donors |
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