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Role of microRNAs in the age-associated decline of pancreatic beta cell function in rat islets
AIMS/HYPOTHESIS: Ageing can lead to reduced insulin sensitivity and loss of pancreatic beta cell function, predisposing individuals to the development of diabetes. The aim of this study was to assess the contribution of microRNAs (miRNAs) to age-associated beta cell dysfunction. METHODS: The global...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670458/ https://www.ncbi.nlm.nih.gov/pubmed/26474776 http://dx.doi.org/10.1007/s00125-015-3783-5 |
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author | Tugay, Ksenia Guay, Claudiane Marques, Ana C. Allagnat, Florent Locke, Jonathan M. Harries, Lorna W. Rutter, Guy A. Regazzi, Romano |
author_facet | Tugay, Ksenia Guay, Claudiane Marques, Ana C. Allagnat, Florent Locke, Jonathan M. Harries, Lorna W. Rutter, Guy A. Regazzi, Romano |
author_sort | Tugay, Ksenia |
collection | PubMed |
description | AIMS/HYPOTHESIS: Ageing can lead to reduced insulin sensitivity and loss of pancreatic beta cell function, predisposing individuals to the development of diabetes. The aim of this study was to assess the contribution of microRNAs (miRNAs) to age-associated beta cell dysfunction. METHODS: The global mRNA and miRNA profiles of 3- and 12-month-old rat islets were collected by microarray. The functional impact of age-associated differences in miRNA expression was investigated by mimicking the observed changes in primary beta cells from young animals. RESULTS: Beta cells from 12-month-old rats retained normal insulin content and secretion, but failed to proliferate in response to mitotic stimuli. The islets of these animals displayed modifications at the level of several miRNAs, including upregulation of miR-34a, miR-124a and miR-383, and downregulation of miR-130b and miR-181a. Computational analysis of the transcriptomic modifications observed in the islets of 12-month-old rats revealed that the differentially expressed genes were enriched for miR-34a and miR-181a targets. Indeed, the induction of miR-34a and reduction of miR-181a in the islets of young animals mimicked the impaired beta cell proliferation observed in old animals. mRNA coding for alpha-type platelet-derived growth factor receptor, which is critical for compensatory beta cell mass expansion, is directly inhibited by miR34a and is likely to be at least partly responsible for the effects of this miRNA. CONCLUSIONS/INTERPRETATION: Changes in the level of specific miRNAs that occur during ageing affect the proliferative capacity of beta cells. This might reduce their ability to expand under conditions of increased insulin demand, favouring the development of type 2 diabetes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00125-015-3783-5) contains peer-reviewed but unedited supplementary material, which is available to authorised users. |
format | Online Article Text |
id | pubmed-4670458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-46704582015-12-14 Role of microRNAs in the age-associated decline of pancreatic beta cell function in rat islets Tugay, Ksenia Guay, Claudiane Marques, Ana C. Allagnat, Florent Locke, Jonathan M. Harries, Lorna W. Rutter, Guy A. Regazzi, Romano Diabetologia Article AIMS/HYPOTHESIS: Ageing can lead to reduced insulin sensitivity and loss of pancreatic beta cell function, predisposing individuals to the development of diabetes. The aim of this study was to assess the contribution of microRNAs (miRNAs) to age-associated beta cell dysfunction. METHODS: The global mRNA and miRNA profiles of 3- and 12-month-old rat islets were collected by microarray. The functional impact of age-associated differences in miRNA expression was investigated by mimicking the observed changes in primary beta cells from young animals. RESULTS: Beta cells from 12-month-old rats retained normal insulin content and secretion, but failed to proliferate in response to mitotic stimuli. The islets of these animals displayed modifications at the level of several miRNAs, including upregulation of miR-34a, miR-124a and miR-383, and downregulation of miR-130b and miR-181a. Computational analysis of the transcriptomic modifications observed in the islets of 12-month-old rats revealed that the differentially expressed genes were enriched for miR-34a and miR-181a targets. Indeed, the induction of miR-34a and reduction of miR-181a in the islets of young animals mimicked the impaired beta cell proliferation observed in old animals. mRNA coding for alpha-type platelet-derived growth factor receptor, which is critical for compensatory beta cell mass expansion, is directly inhibited by miR34a and is likely to be at least partly responsible for the effects of this miRNA. CONCLUSIONS/INTERPRETATION: Changes in the level of specific miRNAs that occur during ageing affect the proliferative capacity of beta cells. This might reduce their ability to expand under conditions of increased insulin demand, favouring the development of type 2 diabetes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00125-015-3783-5) contains peer-reviewed but unedited supplementary material, which is available to authorised users. Springer Berlin Heidelberg 2015-10-16 2016 /pmc/articles/PMC4670458/ /pubmed/26474776 http://dx.doi.org/10.1007/s00125-015-3783-5 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Article Tugay, Ksenia Guay, Claudiane Marques, Ana C. Allagnat, Florent Locke, Jonathan M. Harries, Lorna W. Rutter, Guy A. Regazzi, Romano Role of microRNAs in the age-associated decline of pancreatic beta cell function in rat islets |
title | Role of microRNAs in the age-associated decline of pancreatic beta cell function in rat islets |
title_full | Role of microRNAs in the age-associated decline of pancreatic beta cell function in rat islets |
title_fullStr | Role of microRNAs in the age-associated decline of pancreatic beta cell function in rat islets |
title_full_unstemmed | Role of microRNAs in the age-associated decline of pancreatic beta cell function in rat islets |
title_short | Role of microRNAs in the age-associated decline of pancreatic beta cell function in rat islets |
title_sort | role of micrornas in the age-associated decline of pancreatic beta cell function in rat islets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670458/ https://www.ncbi.nlm.nih.gov/pubmed/26474776 http://dx.doi.org/10.1007/s00125-015-3783-5 |
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