Identification of early biological changes in palmitate-treated isolated human islets

Abstract Background Long-term exposure to elevated levels of free fatty acids (FFAs) is deleterious for beta-cell function and may contribute to development of type 2 diabetes mellitus (T2DM). Whereas mechanisms of impaired glucose-stimulated insulin secretion (GSIS) in FFA-treated beta-cells have b...

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Main Authors: Ernest Sargsyan, Jing Cen, Kirsten Roomp, Reinhard Schneider, Peter Bergsten
Format: Article
Language:English
Published: BMC 2018-08-01
Series:BMC Genomics
Online Access:http://link.springer.com/article/10.1186/s12864-018-5008-z
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author Ernest Sargsyan
Jing Cen
Kirsten Roomp
Reinhard Schneider
Peter Bergsten
author_facet Ernest Sargsyan
Jing Cen
Kirsten Roomp
Reinhard Schneider
Peter Bergsten
author_sort Ernest Sargsyan
collection DOAJ
description Abstract Background Long-term exposure to elevated levels of free fatty acids (FFAs) is deleterious for beta-cell function and may contribute to development of type 2 diabetes mellitus (T2DM). Whereas mechanisms of impaired glucose-stimulated insulin secretion (GSIS) in FFA-treated beta-cells have been intensively studied, biological events preceding the secretory failure, when GSIS is accentuated, are poorly investigated. To identify these early events, we performed genome-wide analysis of gene expression in isolated human islets exposed to fatty acid palmitate for different time periods. Results Palmitate-treated human islets showed decline in beta-cell function starting from day two. Affymetrix Human Transcriptome Array 2.0 identified 903 differentially expressed genes (DEGs). Mapping of the genes onto pathways using KEGG pathway enrichment analysis predicted four islet biology-related pathways enriched prior but not after the decline of islet function and three pathways enriched both prior and after the decline of islet function. DEGs from these pathways were analyzed at the transcript level. The results propose that in palmitate-treated human islets, at early time points, protective events, including up-regulation of metallothioneins, tRNA synthetases and fatty acid-metabolising proteins, dominate over deleterious events, including inhibition of fatty acid detoxification enzymes, which contributes to the enhanced GSIS. After prolonged exposure of islets to palmitate, the protective events are outweighed by the deleterious events, which leads to impaired GSIS. Conclusions The study identifies temporal order between different cellular events, which either promote or protect from beta-cell failure. The sequence of these events should be considered when developing strategies for prevention and treatment of the disease.
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spelling doaj.art-822eedc2b8a94c5e8fb0068b109b8e122022-12-22T01:14:06ZengBMCBMC Genomics1471-21642018-08-0119111110.1186/s12864-018-5008-zIdentification of early biological changes in palmitate-treated isolated human isletsErnest Sargsyan0Jing Cen1Kirsten Roomp2Reinhard Schneider3Peter Bergsten4Department of Medical Cell Biology, Uppsala UniversityDepartment of Medical Cell Biology, Uppsala UniversityLuxembourg Centre for Systems Biomedicine, University of LuxembourgLuxembourg Centre for Systems Biomedicine, University of LuxembourgDepartment of Medical Cell Biology, Uppsala UniversityAbstract Background Long-term exposure to elevated levels of free fatty acids (FFAs) is deleterious for beta-cell function and may contribute to development of type 2 diabetes mellitus (T2DM). Whereas mechanisms of impaired glucose-stimulated insulin secretion (GSIS) in FFA-treated beta-cells have been intensively studied, biological events preceding the secretory failure, when GSIS is accentuated, are poorly investigated. To identify these early events, we performed genome-wide analysis of gene expression in isolated human islets exposed to fatty acid palmitate for different time periods. Results Palmitate-treated human islets showed decline in beta-cell function starting from day two. Affymetrix Human Transcriptome Array 2.0 identified 903 differentially expressed genes (DEGs). Mapping of the genes onto pathways using KEGG pathway enrichment analysis predicted four islet biology-related pathways enriched prior but not after the decline of islet function and three pathways enriched both prior and after the decline of islet function. DEGs from these pathways were analyzed at the transcript level. The results propose that in palmitate-treated human islets, at early time points, protective events, including up-regulation of metallothioneins, tRNA synthetases and fatty acid-metabolising proteins, dominate over deleterious events, including inhibition of fatty acid detoxification enzymes, which contributes to the enhanced GSIS. After prolonged exposure of islets to palmitate, the protective events are outweighed by the deleterious events, which leads to impaired GSIS. Conclusions The study identifies temporal order between different cellular events, which either promote or protect from beta-cell failure. The sequence of these events should be considered when developing strategies for prevention and treatment of the disease.http://link.springer.com/article/10.1186/s12864-018-5008-z
spellingShingle Ernest Sargsyan
Jing Cen
Kirsten Roomp
Reinhard Schneider
Peter Bergsten
Identification of early biological changes in palmitate-treated isolated human islets
BMC Genomics
title Identification of early biological changes in palmitate-treated isolated human islets
title_full Identification of early biological changes in palmitate-treated isolated human islets
title_fullStr Identification of early biological changes in palmitate-treated isolated human islets
title_full_unstemmed Identification of early biological changes in palmitate-treated isolated human islets
title_short Identification of early biological changes in palmitate-treated isolated human islets
title_sort identification of early biological changes in palmitate treated isolated human islets
url http://link.springer.com/article/10.1186/s12864-018-5008-z
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