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Understanding diverse TRPV1 signaling – an update
The transient receptor potential vanilloid 1 (TRPV1) is densely expressed in spinal sensory neurons as well as in cranial sensory neurons, including their central terminal endings. Recent work in the less familiar cranial sensory neurons, despite their many similarities with spinal sensory neurons,...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000 Research Limited
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880261/ https://www.ncbi.nlm.nih.gov/pubmed/31824648 http://dx.doi.org/10.12688/f1000research.20795.1 |
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author | Andresen, Michael C. |
author_facet | Andresen, Michael C. |
author_sort | Andresen, Michael C. |
collection | PubMed |
description | The transient receptor potential vanilloid 1 (TRPV1) is densely expressed in spinal sensory neurons as well as in cranial sensory neurons, including their central terminal endings. Recent work in the less familiar cranial sensory neurons, despite their many similarities with spinal sensory neurons, suggest that TRPV1 acts as a calcium channel to release a discrete population of synaptic vesicles. The modular and independent regulation of release offers new questions about nanodomain organization of release and selective actions of G protein–coupled receptors. |
format | Online Article Text |
id | pubmed-6880261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-68802612019-12-09 Understanding diverse TRPV1 signaling – an update Andresen, Michael C. F1000Res Review The transient receptor potential vanilloid 1 (TRPV1) is densely expressed in spinal sensory neurons as well as in cranial sensory neurons, including their central terminal endings. Recent work in the less familiar cranial sensory neurons, despite their many similarities with spinal sensory neurons, suggest that TRPV1 acts as a calcium channel to release a discrete population of synaptic vesicles. The modular and independent regulation of release offers new questions about nanodomain organization of release and selective actions of G protein–coupled receptors. F1000 Research Limited 2019-11-25 /pmc/articles/PMC6880261/ /pubmed/31824648 http://dx.doi.org/10.12688/f1000research.20795.1 Text en Copyright: © 2019 Andresen MC http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Andresen, Michael C. Understanding diverse TRPV1 signaling – an update |
title | Understanding diverse TRPV1 signaling – an update |
title_full | Understanding diverse TRPV1 signaling – an update |
title_fullStr | Understanding diverse TRPV1 signaling – an update |
title_full_unstemmed | Understanding diverse TRPV1 signaling – an update |
title_short | Understanding diverse TRPV1 signaling – an update |
title_sort | understanding diverse trpv1 signaling – an update |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880261/ https://www.ncbi.nlm.nih.gov/pubmed/31824648 http://dx.doi.org/10.12688/f1000research.20795.1 |
work_keys_str_mv | AT andresenmichaelc understandingdiversetrpv1signalinganupdate |