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Differential Gene Expression in GPR40-Overexpressing Pancreatic β-cells Treated with Linoleic Acid

"G protein-coupled receptor 40" (GPR40), a receptor for long-chain fatty acids, mediates the stimulation of glucose-induced insulin secretion. We examined the profiles of differential gene expression in GPR40-activated cells treated with linoleic acid, and finally predicted the integral pa...

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Autores principales: Kim, In-Su, Yang, So-Young, Han, Joo-Hui, Jung, Sang-Hyuk, Park, Hyun-Soo, Myung, Chang-Seon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342734/
https://www.ncbi.nlm.nih.gov/pubmed/25729276
http://dx.doi.org/10.4196/kjpp.2015.19.2.141
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author Kim, In-Su
Yang, So-Young
Han, Joo-Hui
Jung, Sang-Hyuk
Park, Hyun-Soo
Myung, Chang-Seon
author_facet Kim, In-Su
Yang, So-Young
Han, Joo-Hui
Jung, Sang-Hyuk
Park, Hyun-Soo
Myung, Chang-Seon
author_sort Kim, In-Su
collection PubMed
description "G protein-coupled receptor 40" (GPR40), a receptor for long-chain fatty acids, mediates the stimulation of glucose-induced insulin secretion. We examined the profiles of differential gene expression in GPR40-activated cells treated with linoleic acid, and finally predicted the integral pathways of the cellular mechanism of GPR40-mediated insulinotropic effects. After constructing a GPR40-overexpressing stable cell line (RIN-40) from the rat pancreatic β-cell line RIN-5f, we determined the gene expression profiles of RIN-5f and RIN-40. In total, 1004 genes, the expression of which was altered at least twofold, were selected in RIN-5f versus RIN-40. Moreover, the differential genetic profiles were investigated in RIN-40 cells treated with 30 µM linoleic acid, which resulted in selection of 93 genes in RIN-40 versus RIN-40 treated with linoleic acid. Based on the Kyoto Encyclopedia of Genes and Genomes Pathway (KEGG, http://www.genome.jp/kegg/), sets of genes induced differentially by treatment with linoleic acid in RIN-40 cells were found to be related to mitogen-activated protein (MAP) kinase- and neuroactive ligand-receptor interaction pathways. A gene ontology (GO) study revealed that more than 30% of the genes were associated with signal transduction and cell proliferation. Thus, this study elucidated a gene expression pattern relevant to the signal pathways that are regulated by GPR40 activation during the acute period. Together, these findings increase our mechanistic understanding of endogenous molecules associated with GPR40 function, and provide information useful for identification of a target for the management of type 2 diabetes mellitus.
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spelling pubmed-43427342015-03-01 Differential Gene Expression in GPR40-Overexpressing Pancreatic β-cells Treated with Linoleic Acid Kim, In-Su Yang, So-Young Han, Joo-Hui Jung, Sang-Hyuk Park, Hyun-Soo Myung, Chang-Seon Korean J Physiol Pharmacol Original Article "G protein-coupled receptor 40" (GPR40), a receptor for long-chain fatty acids, mediates the stimulation of glucose-induced insulin secretion. We examined the profiles of differential gene expression in GPR40-activated cells treated with linoleic acid, and finally predicted the integral pathways of the cellular mechanism of GPR40-mediated insulinotropic effects. After constructing a GPR40-overexpressing stable cell line (RIN-40) from the rat pancreatic β-cell line RIN-5f, we determined the gene expression profiles of RIN-5f and RIN-40. In total, 1004 genes, the expression of which was altered at least twofold, were selected in RIN-5f versus RIN-40. Moreover, the differential genetic profiles were investigated in RIN-40 cells treated with 30 µM linoleic acid, which resulted in selection of 93 genes in RIN-40 versus RIN-40 treated with linoleic acid. Based on the Kyoto Encyclopedia of Genes and Genomes Pathway (KEGG, http://www.genome.jp/kegg/), sets of genes induced differentially by treatment with linoleic acid in RIN-40 cells were found to be related to mitogen-activated protein (MAP) kinase- and neuroactive ligand-receptor interaction pathways. A gene ontology (GO) study revealed that more than 30% of the genes were associated with signal transduction and cell proliferation. Thus, this study elucidated a gene expression pattern relevant to the signal pathways that are regulated by GPR40 activation during the acute period. Together, these findings increase our mechanistic understanding of endogenous molecules associated with GPR40 function, and provide information useful for identification of a target for the management of type 2 diabetes mellitus. The Korean Physiological Society and The Korean Society of Pharmacology 2015-03 2015-02-25 /pmc/articles/PMC4342734/ /pubmed/25729276 http://dx.doi.org/10.4196/kjpp.2015.19.2.141 Text en Copyright © 2015 The Korean Physiological Society and The Korean Society of Pharmacology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, In-Su
Yang, So-Young
Han, Joo-Hui
Jung, Sang-Hyuk
Park, Hyun-Soo
Myung, Chang-Seon
Differential Gene Expression in GPR40-Overexpressing Pancreatic β-cells Treated with Linoleic Acid
title Differential Gene Expression in GPR40-Overexpressing Pancreatic β-cells Treated with Linoleic Acid
title_full Differential Gene Expression in GPR40-Overexpressing Pancreatic β-cells Treated with Linoleic Acid
title_fullStr Differential Gene Expression in GPR40-Overexpressing Pancreatic β-cells Treated with Linoleic Acid
title_full_unstemmed Differential Gene Expression in GPR40-Overexpressing Pancreatic β-cells Treated with Linoleic Acid
title_short Differential Gene Expression in GPR40-Overexpressing Pancreatic β-cells Treated with Linoleic Acid
title_sort differential gene expression in gpr40-overexpressing pancreatic β-cells treated with linoleic acid
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342734/
https://www.ncbi.nlm.nih.gov/pubmed/25729276
http://dx.doi.org/10.4196/kjpp.2015.19.2.141
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