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Maternal whole blood cell miRNA-340 is elevated in gestational diabetes and inversely regulated by glucose and insulin
The number of pregnancies complicated by gestational diabetes (GDM) is increasing worldwide. To identify novel characteristics of GDM, we studied miRNA profiles of maternal and fetal whole blood cells (WBCs) from GDM and normal glucose tolerant (NGT) pregnant women matched for body mass index and ma...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778051/ https://www.ncbi.nlm.nih.gov/pubmed/29358694 http://dx.doi.org/10.1038/s41598-018-19200-9 |
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author | Stirm, Laura Huypens, Peter Sass, Steffen Batra, Richa Fritsche, Louise Brucker, Sara Abele, Harald Hennige, Anita M. Theis, Fabian Beckers, Johannes Hrabě de Angelis, Martin Fritsche, Andreas Häring, Hans-Ulrich Staiger, Harald |
author_facet | Stirm, Laura Huypens, Peter Sass, Steffen Batra, Richa Fritsche, Louise Brucker, Sara Abele, Harald Hennige, Anita M. Theis, Fabian Beckers, Johannes Hrabě de Angelis, Martin Fritsche, Andreas Häring, Hans-Ulrich Staiger, Harald |
author_sort | Stirm, Laura |
collection | PubMed |
description | The number of pregnancies complicated by gestational diabetes (GDM) is increasing worldwide. To identify novel characteristics of GDM, we studied miRNA profiles of maternal and fetal whole blood cells (WBCs) from GDM and normal glucose tolerant (NGT) pregnant women matched for body mass index and maternal age. After adjustment for maternal weight gain and pregnancy week, we identified 29 mature micro-RNAs (miRNAs) up-regulated in GDM, one of which, i.e., miRNA-340, was validated by qPCR. mRNA and protein expression of PAIP1, a miRNA-340 target gene, was found down-regulated in GDM women, accordingly. In lymphocytes derived from the mothers’ blood and treated in vitro, insulin increased and glucose reduced miRNA-340 expression. In fetal cord blood samples, no associations of miRNA-340 with maternal GDM were observed. Our results provide evidence for insulin-induced epigenetic, i.e., miRNA-dependent, programming of maternal WBCs in GDM. |
format | Online Article Text |
id | pubmed-5778051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57780512018-01-31 Maternal whole blood cell miRNA-340 is elevated in gestational diabetes and inversely regulated by glucose and insulin Stirm, Laura Huypens, Peter Sass, Steffen Batra, Richa Fritsche, Louise Brucker, Sara Abele, Harald Hennige, Anita M. Theis, Fabian Beckers, Johannes Hrabě de Angelis, Martin Fritsche, Andreas Häring, Hans-Ulrich Staiger, Harald Sci Rep Article The number of pregnancies complicated by gestational diabetes (GDM) is increasing worldwide. To identify novel characteristics of GDM, we studied miRNA profiles of maternal and fetal whole blood cells (WBCs) from GDM and normal glucose tolerant (NGT) pregnant women matched for body mass index and maternal age. After adjustment for maternal weight gain and pregnancy week, we identified 29 mature micro-RNAs (miRNAs) up-regulated in GDM, one of which, i.e., miRNA-340, was validated by qPCR. mRNA and protein expression of PAIP1, a miRNA-340 target gene, was found down-regulated in GDM women, accordingly. In lymphocytes derived from the mothers’ blood and treated in vitro, insulin increased and glucose reduced miRNA-340 expression. In fetal cord blood samples, no associations of miRNA-340 with maternal GDM were observed. Our results provide evidence for insulin-induced epigenetic, i.e., miRNA-dependent, programming of maternal WBCs in GDM. Nature Publishing Group UK 2018-01-22 /pmc/articles/PMC5778051/ /pubmed/29358694 http://dx.doi.org/10.1038/s41598-018-19200-9 Text en © The Author(s) 2018 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 Stirm, Laura Huypens, Peter Sass, Steffen Batra, Richa Fritsche, Louise Brucker, Sara Abele, Harald Hennige, Anita M. Theis, Fabian Beckers, Johannes Hrabě de Angelis, Martin Fritsche, Andreas Häring, Hans-Ulrich Staiger, Harald Maternal whole blood cell miRNA-340 is elevated in gestational diabetes and inversely regulated by glucose and insulin |
title | Maternal whole blood cell miRNA-340 is elevated in gestational diabetes and inversely regulated by glucose and insulin |
title_full | Maternal whole blood cell miRNA-340 is elevated in gestational diabetes and inversely regulated by glucose and insulin |
title_fullStr | Maternal whole blood cell miRNA-340 is elevated in gestational diabetes and inversely regulated by glucose and insulin |
title_full_unstemmed | Maternal whole blood cell miRNA-340 is elevated in gestational diabetes and inversely regulated by glucose and insulin |
title_short | Maternal whole blood cell miRNA-340 is elevated in gestational diabetes and inversely regulated by glucose and insulin |
title_sort | maternal whole blood cell mirna-340 is elevated in gestational diabetes and inversely regulated by glucose and insulin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778051/ https://www.ncbi.nlm.nih.gov/pubmed/29358694 http://dx.doi.org/10.1038/s41598-018-19200-9 |
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