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Olfactory receptor 10J5 responding to α-cedrene regulates hepatic steatosis via the cAMP–PKA pathway

Ectopic expression and functions of odorant receptors (ORs) in the human body have aroused much interest in the past decade. Mouse olfactory receptor 23 (MOR23, olfr16) and its human orthologue, OR10J5, have been found to be functionally expressed in several non-olfactory systems. Here, using MOR23-...

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Autores principales: Tong, Tao, Ryu, Sang Eun, Min, Yeojin, de March, Claire A., Bushdid, Caroline, Golebiowski, Jérôme, Moon, Cheil, Park, Taesun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573314/
https://www.ncbi.nlm.nih.gov/pubmed/28842679
http://dx.doi.org/10.1038/s41598-017-10379-x
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author Tong, Tao
Ryu, Sang Eun
Min, Yeojin
de March, Claire A.
Bushdid, Caroline
Golebiowski, Jérôme
Moon, Cheil
Park, Taesun
author_facet Tong, Tao
Ryu, Sang Eun
Min, Yeojin
de March, Claire A.
Bushdid, Caroline
Golebiowski, Jérôme
Moon, Cheil
Park, Taesun
author_sort Tong, Tao
collection PubMed
description Ectopic expression and functions of odorant receptors (ORs) in the human body have aroused much interest in the past decade. Mouse olfactory receptor 23 (MOR23, olfr16) and its human orthologue, OR10J5, have been found to be functionally expressed in several non-olfactory systems. Here, using MOR23- and OR10J5-expressing Hana3A cells, we identified α-cedrene, a natural compound that protects against hepatic steatosis in mice fed the high-fat diet, as a novel agonist of these receptors. In human hepatocytes, an RNA interference-mediated knockdown of OR10J5 increased intracellular lipid accumulation, along with upregulation of lipogenic genes and downregulation of genes related to fatty acid oxidation. α-Cedrene stimulation resulted in a significant reduction in lipid contents of human hepatocytes and reprogramming of metabolic signatures, which are mediated by OR10J5, as demonstrated by receptor knockdown experiments using RNA interference. Taken together, our findings show a crucial role of OR10J5 in the regulation of lipid accumulation in human hepatocytes.
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spelling pubmed-55733142017-09-01 Olfactory receptor 10J5 responding to α-cedrene regulates hepatic steatosis via the cAMP–PKA pathway Tong, Tao Ryu, Sang Eun Min, Yeojin de March, Claire A. Bushdid, Caroline Golebiowski, Jérôme Moon, Cheil Park, Taesun Sci Rep Article Ectopic expression and functions of odorant receptors (ORs) in the human body have aroused much interest in the past decade. Mouse olfactory receptor 23 (MOR23, olfr16) and its human orthologue, OR10J5, have been found to be functionally expressed in several non-olfactory systems. Here, using MOR23- and OR10J5-expressing Hana3A cells, we identified α-cedrene, a natural compound that protects against hepatic steatosis in mice fed the high-fat diet, as a novel agonist of these receptors. In human hepatocytes, an RNA interference-mediated knockdown of OR10J5 increased intracellular lipid accumulation, along with upregulation of lipogenic genes and downregulation of genes related to fatty acid oxidation. α-Cedrene stimulation resulted in a significant reduction in lipid contents of human hepatocytes and reprogramming of metabolic signatures, which are mediated by OR10J5, as demonstrated by receptor knockdown experiments using RNA interference. Taken together, our findings show a crucial role of OR10J5 in the regulation of lipid accumulation in human hepatocytes. Nature Publishing Group UK 2017-08-25 /pmc/articles/PMC5573314/ /pubmed/28842679 http://dx.doi.org/10.1038/s41598-017-10379-x Text en © The Author(s) 2017 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/.
spellingShingle Article
Tong, Tao
Ryu, Sang Eun
Min, Yeojin
de March, Claire A.
Bushdid, Caroline
Golebiowski, Jérôme
Moon, Cheil
Park, Taesun
Olfactory receptor 10J5 responding to α-cedrene regulates hepatic steatosis via the cAMP–PKA pathway
title Olfactory receptor 10J5 responding to α-cedrene regulates hepatic steatosis via the cAMP–PKA pathway
title_full Olfactory receptor 10J5 responding to α-cedrene regulates hepatic steatosis via the cAMP–PKA pathway
title_fullStr Olfactory receptor 10J5 responding to α-cedrene regulates hepatic steatosis via the cAMP–PKA pathway
title_full_unstemmed Olfactory receptor 10J5 responding to α-cedrene regulates hepatic steatosis via the cAMP–PKA pathway
title_short Olfactory receptor 10J5 responding to α-cedrene regulates hepatic steatosis via the cAMP–PKA pathway
title_sort olfactory receptor 10j5 responding to α-cedrene regulates hepatic steatosis via the camp–pka pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573314/
https://www.ncbi.nlm.nih.gov/pubmed/28842679
http://dx.doi.org/10.1038/s41598-017-10379-x
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