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Antibodies to the Extracellular Pore Loop of TRPM8 Act as Antagonists of Channel Activation
The mammalian transient receptor potential melastatin channel 8 (TRPM8) is highly expressed in trigeminal and dorsal root ganglia. TRPM8 is activated by cold temperature or compounds that cause a cooling sensation, such as menthol or icilin. TRPM8 may play a role in cold hypersensitivity and hyperal...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159296/ https://www.ncbi.nlm.nih.gov/pubmed/25203266 http://dx.doi.org/10.1371/journal.pone.0107151 |
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author | Miller, Silke Rao, Sara Wang, Weiya Liu, Hantao Wang, Judy Gavva, Narender R. |
author_facet | Miller, Silke Rao, Sara Wang, Weiya Liu, Hantao Wang, Judy Gavva, Narender R. |
author_sort | Miller, Silke |
collection | PubMed |
description | The mammalian transient receptor potential melastatin channel 8 (TRPM8) is highly expressed in trigeminal and dorsal root ganglia. TRPM8 is activated by cold temperature or compounds that cause a cooling sensation, such as menthol or icilin. TRPM8 may play a role in cold hypersensitivity and hyperalgesia in various pain syndromes. Therefore, TRPM8 antagonists are pursued as therapeutics. In this study we explored the feasibility of blocking TRPM8 activation with antibodies. We report the functional characterization of a rabbit polyclonal antibody, ACC-049, directed against the third extracellular loop near the pore region of the human TRPM8 channel. ACC-049 acted as a full antagonist at recombinantly expressed human and rodent TRPM8 channels in cell based agonist-induced (45)Ca(2+) uptake assays. Further, several poly-and monoclonal antibodies that recognize the same region also blocked icilin activation of not only recombinantly expressed TRPM8, but also endogenous TRPM8 expressed in rat dorsal root ganglion neurons revealing the feasibility of generating monoclonal antibody antagonists. We conclude that antagonist antibodies are valuable tools to investigate TRPM8 function and may ultimately pave the way for development of therapeutic antibodies. |
format | Online Article Text |
id | pubmed-4159296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41592962014-09-12 Antibodies to the Extracellular Pore Loop of TRPM8 Act as Antagonists of Channel Activation Miller, Silke Rao, Sara Wang, Weiya Liu, Hantao Wang, Judy Gavva, Narender R. PLoS One Research Article The mammalian transient receptor potential melastatin channel 8 (TRPM8) is highly expressed in trigeminal and dorsal root ganglia. TRPM8 is activated by cold temperature or compounds that cause a cooling sensation, such as menthol or icilin. TRPM8 may play a role in cold hypersensitivity and hyperalgesia in various pain syndromes. Therefore, TRPM8 antagonists are pursued as therapeutics. In this study we explored the feasibility of blocking TRPM8 activation with antibodies. We report the functional characterization of a rabbit polyclonal antibody, ACC-049, directed against the third extracellular loop near the pore region of the human TRPM8 channel. ACC-049 acted as a full antagonist at recombinantly expressed human and rodent TRPM8 channels in cell based agonist-induced (45)Ca(2+) uptake assays. Further, several poly-and monoclonal antibodies that recognize the same region also blocked icilin activation of not only recombinantly expressed TRPM8, but also endogenous TRPM8 expressed in rat dorsal root ganglion neurons revealing the feasibility of generating monoclonal antibody antagonists. We conclude that antagonist antibodies are valuable tools to investigate TRPM8 function and may ultimately pave the way for development of therapeutic antibodies. Public Library of Science 2014-09-09 /pmc/articles/PMC4159296/ /pubmed/25203266 http://dx.doi.org/10.1371/journal.pone.0107151 Text en © 2014 Miller et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Miller, Silke Rao, Sara Wang, Weiya Liu, Hantao Wang, Judy Gavva, Narender R. Antibodies to the Extracellular Pore Loop of TRPM8 Act as Antagonists of Channel Activation |
title | Antibodies to the Extracellular Pore Loop of TRPM8 Act as Antagonists of Channel Activation |
title_full | Antibodies to the Extracellular Pore Loop of TRPM8 Act as Antagonists of Channel Activation |
title_fullStr | Antibodies to the Extracellular Pore Loop of TRPM8 Act as Antagonists of Channel Activation |
title_full_unstemmed | Antibodies to the Extracellular Pore Loop of TRPM8 Act as Antagonists of Channel Activation |
title_short | Antibodies to the Extracellular Pore Loop of TRPM8 Act as Antagonists of Channel Activation |
title_sort | antibodies to the extracellular pore loop of trpm8 act as antagonists of channel activation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159296/ https://www.ncbi.nlm.nih.gov/pubmed/25203266 http://dx.doi.org/10.1371/journal.pone.0107151 |
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