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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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