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Pirt Functions as an Endogenous Regulator of TRPM8
Pirt is a membrane protein that is specifically expressed in the peripheral nervous system, where it has been shown to increase the sensitivity of the transient receptor potential vanilloid 1 (TRPV1) channel and modulate its role in heat pain. The broad expression of Pirt among dorsal root ganglion...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748931/ https://www.ncbi.nlm.nih.gov/pubmed/23863968 http://dx.doi.org/10.1038/ncomms3179 |
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author | Tang, Zongxiang Kim, Andrew Masuch, Thorsten Park, Kyoungsook Weng, HaoJui Wetzel, Christian Dong, Xinzhong |
author_facet | Tang, Zongxiang Kim, Andrew Masuch, Thorsten Park, Kyoungsook Weng, HaoJui Wetzel, Christian Dong, Xinzhong |
author_sort | Tang, Zongxiang |
collection | PubMed |
description | Pirt is a membrane protein that is specifically expressed in the peripheral nervous system, where it has been shown to increase the sensitivity of the transient receptor potential vanilloid 1 (TRPV1) channel and modulate its role in heat pain. The broad expression of Pirt among dorsal root ganglion neurons suggests it may modulate other TRPs, such as the menthol and cooling sensor TRPM8. The discrepancies in the channel properties of TRPM8 in native neurons versus heterologous cells indicate the existence of endogenous modulators of the channel. Here we show that Pirt regulates the function of TRPM8 and its role in detecting cold. Pirt(−/−) mice exhibit decreased behavioral responses to cold and cool temperatures, and Pirt increases the sensitivity of TRPM8 to menthol and cool temperature. Our data suggest Pirt is an endogenous regulator of TRPM8. |
format | Online Article Text |
id | pubmed-3748931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-37489312014-01-17 Pirt Functions as an Endogenous Regulator of TRPM8 Tang, Zongxiang Kim, Andrew Masuch, Thorsten Park, Kyoungsook Weng, HaoJui Wetzel, Christian Dong, Xinzhong Nat Commun Article Pirt is a membrane protein that is specifically expressed in the peripheral nervous system, where it has been shown to increase the sensitivity of the transient receptor potential vanilloid 1 (TRPV1) channel and modulate its role in heat pain. The broad expression of Pirt among dorsal root ganglion neurons suggests it may modulate other TRPs, such as the menthol and cooling sensor TRPM8. The discrepancies in the channel properties of TRPM8 in native neurons versus heterologous cells indicate the existence of endogenous modulators of the channel. Here we show that Pirt regulates the function of TRPM8 and its role in detecting cold. Pirt(−/−) mice exhibit decreased behavioral responses to cold and cool temperatures, and Pirt increases the sensitivity of TRPM8 to menthol and cool temperature. Our data suggest Pirt is an endogenous regulator of TRPM8. 2013 /pmc/articles/PMC3748931/ /pubmed/23863968 http://dx.doi.org/10.1038/ncomms3179 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Tang, Zongxiang Kim, Andrew Masuch, Thorsten Park, Kyoungsook Weng, HaoJui Wetzel, Christian Dong, Xinzhong Pirt Functions as an Endogenous Regulator of TRPM8 |
title | Pirt Functions as an Endogenous Regulator of TRPM8 |
title_full | Pirt Functions as an Endogenous Regulator of TRPM8 |
title_fullStr | Pirt Functions as an Endogenous Regulator of TRPM8 |
title_full_unstemmed | Pirt Functions as an Endogenous Regulator of TRPM8 |
title_short | Pirt Functions as an Endogenous Regulator of TRPM8 |
title_sort | pirt functions as an endogenous regulator of trpm8 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748931/ https://www.ncbi.nlm.nih.gov/pubmed/23863968 http://dx.doi.org/10.1038/ncomms3179 |
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