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Identification of G protein-coupled receptor 55 (GPR55) as a target of curcumin
The identification of molecular targets of bioactive food components is important to understand the mechanistic aspect of their physiological functions. Here, we have developed a screening system that enables us to determine the activation of G protein-coupled receptors (GPCRs) by food components an...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760322/ https://www.ncbi.nlm.nih.gov/pubmed/35031622 http://dx.doi.org/10.1038/s41538-021-00119-x |
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author | Harada, Naoki Okuyama, Mai Teraoka, Yoshiaki Arahori, Yumi Shinmori, Yoh Horiuchi, Hiroko Luis, Paula B. Joseph, Akil I. Kitakaze, Tomoya Matsumura, Shigenobu Hira, Tohru Yamamoto, Norio Iuni, Takashi Goshima, Naoki Schneider, Claus Inui, Hiroshi Yamaji, Ryoichi |
author_facet | Harada, Naoki Okuyama, Mai Teraoka, Yoshiaki Arahori, Yumi Shinmori, Yoh Horiuchi, Hiroko Luis, Paula B. Joseph, Akil I. Kitakaze, Tomoya Matsumura, Shigenobu Hira, Tohru Yamamoto, Norio Iuni, Takashi Goshima, Naoki Schneider, Claus Inui, Hiroshi Yamaji, Ryoichi |
author_sort | Harada, Naoki |
collection | PubMed |
description | The identification of molecular targets of bioactive food components is important to understand the mechanistic aspect of their physiological functions. Here, we have developed a screening system that enables us to determine the activation of G protein-coupled receptors (GPCRs) by food components and have identified GPR55 as a target for curcumin. Curcumin activated GPR55 and induced serum-response element- and serum-response factor-mediated transcription, which were inhibited by Rho kinase and GPR55 antagonists. Both the methoxy group and the heptadienone moiety of curcumin were required for GPR55 activation. The F190(5.47) residue of GPR55 was important for the interaction with curcumin. The curcumin-induced secretion of glucagon-like peptide-1 in GLUTag cells was inhibited by a GPR55 antagonist. These results indicate that expression screening is a useful system to identify GPCRs as targets of food components and strongly suggest that curcumin activates GPR55 as an agonist, which is involved in the physiological function of curcumin. |
format | Online Article Text |
id | pubmed-8760322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87603222022-01-26 Identification of G protein-coupled receptor 55 (GPR55) as a target of curcumin Harada, Naoki Okuyama, Mai Teraoka, Yoshiaki Arahori, Yumi Shinmori, Yoh Horiuchi, Hiroko Luis, Paula B. Joseph, Akil I. Kitakaze, Tomoya Matsumura, Shigenobu Hira, Tohru Yamamoto, Norio Iuni, Takashi Goshima, Naoki Schneider, Claus Inui, Hiroshi Yamaji, Ryoichi NPJ Sci Food Article The identification of molecular targets of bioactive food components is important to understand the mechanistic aspect of their physiological functions. Here, we have developed a screening system that enables us to determine the activation of G protein-coupled receptors (GPCRs) by food components and have identified GPR55 as a target for curcumin. Curcumin activated GPR55 and induced serum-response element- and serum-response factor-mediated transcription, which were inhibited by Rho kinase and GPR55 antagonists. Both the methoxy group and the heptadienone moiety of curcumin were required for GPR55 activation. The F190(5.47) residue of GPR55 was important for the interaction with curcumin. The curcumin-induced secretion of glucagon-like peptide-1 in GLUTag cells was inhibited by a GPR55 antagonist. These results indicate that expression screening is a useful system to identify GPCRs as targets of food components and strongly suggest that curcumin activates GPR55 as an agonist, which is involved in the physiological function of curcumin. Nature Publishing Group UK 2022-01-14 /pmc/articles/PMC8760322/ /pubmed/35031622 http://dx.doi.org/10.1038/s41538-021-00119-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Harada, Naoki Okuyama, Mai Teraoka, Yoshiaki Arahori, Yumi Shinmori, Yoh Horiuchi, Hiroko Luis, Paula B. Joseph, Akil I. Kitakaze, Tomoya Matsumura, Shigenobu Hira, Tohru Yamamoto, Norio Iuni, Takashi Goshima, Naoki Schneider, Claus Inui, Hiroshi Yamaji, Ryoichi Identification of G protein-coupled receptor 55 (GPR55) as a target of curcumin |
title | Identification of G protein-coupled receptor 55 (GPR55) as a target of curcumin |
title_full | Identification of G protein-coupled receptor 55 (GPR55) as a target of curcumin |
title_fullStr | Identification of G protein-coupled receptor 55 (GPR55) as a target of curcumin |
title_full_unstemmed | Identification of G protein-coupled receptor 55 (GPR55) as a target of curcumin |
title_short | Identification of G protein-coupled receptor 55 (GPR55) as a target of curcumin |
title_sort | identification of g protein-coupled receptor 55 (gpr55) as a target of curcumin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760322/ https://www.ncbi.nlm.nih.gov/pubmed/35031622 http://dx.doi.org/10.1038/s41538-021-00119-x |
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