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Sensitization of TRPA1 by Protein Kinase A

The TRPA1 ion channel is expressed in nociceptive (pain-sensitive) somatosensory neurons and is activated by a wide variety of chemical irritants, such as acrolein in smoke or isothiocyanates in mustard. Here, we investigate the enhancement of TRPA1 function caused by inflammatory mediators, which i...

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Detalles Bibliográficos
Autores principales: Meents, Jannis E., Fischer, Michael J. M., McNaughton, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226813/
https://www.ncbi.nlm.nih.gov/pubmed/28076424
http://dx.doi.org/10.1371/journal.pone.0170097
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author Meents, Jannis E.
Fischer, Michael J. M.
McNaughton, Peter A.
author_facet Meents, Jannis E.
Fischer, Michael J. M.
McNaughton, Peter A.
author_sort Meents, Jannis E.
collection PubMed
description The TRPA1 ion channel is expressed in nociceptive (pain-sensitive) somatosensory neurons and is activated by a wide variety of chemical irritants, such as acrolein in smoke or isothiocyanates in mustard. Here, we investigate the enhancement of TRPA1 function caused by inflammatory mediators, which is thought to be important in lung conditions such as asthma and COPD. Protein kinase A is an important kinase acting downstream of inflammatory mediators to cause sensitization of TRPA1. By using site-directed mutagenesis, patch-clamp electrophysiology and calcium imaging we identify four amino acid residues, S86, S317, S428, and S972, as the principal targets of PKA-mediated phosphorylation and sensitization of TRPA1.
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spelling pubmed-52268132017-01-31 Sensitization of TRPA1 by Protein Kinase A Meents, Jannis E. Fischer, Michael J. M. McNaughton, Peter A. PLoS One Research Article The TRPA1 ion channel is expressed in nociceptive (pain-sensitive) somatosensory neurons and is activated by a wide variety of chemical irritants, such as acrolein in smoke or isothiocyanates in mustard. Here, we investigate the enhancement of TRPA1 function caused by inflammatory mediators, which is thought to be important in lung conditions such as asthma and COPD. Protein kinase A is an important kinase acting downstream of inflammatory mediators to cause sensitization of TRPA1. By using site-directed mutagenesis, patch-clamp electrophysiology and calcium imaging we identify four amino acid residues, S86, S317, S428, and S972, as the principal targets of PKA-mediated phosphorylation and sensitization of TRPA1. Public Library of Science 2017-01-11 /pmc/articles/PMC5226813/ /pubmed/28076424 http://dx.doi.org/10.1371/journal.pone.0170097 Text en © 2017 Meents 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Meents, Jannis E.
Fischer, Michael J. M.
McNaughton, Peter A.
Sensitization of TRPA1 by Protein Kinase A
title Sensitization of TRPA1 by Protein Kinase A
title_full Sensitization of TRPA1 by Protein Kinase A
title_fullStr Sensitization of TRPA1 by Protein Kinase A
title_full_unstemmed Sensitization of TRPA1 by Protein Kinase A
title_short Sensitization of TRPA1 by Protein Kinase A
title_sort sensitization of trpa1 by protein kinase a
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226813/
https://www.ncbi.nlm.nih.gov/pubmed/28076424
http://dx.doi.org/10.1371/journal.pone.0170097
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