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MiR-199a-5p regulates sirtuin1 and PI3K in the rat hippocampus with intrauterine growth restriction
In humans, malnutrition during pregnancy results in intrauterine growth restriction (IUGR) and an increased risk of neurological morbidities; altered miRNA characteristics have been suggested to contribute to IUGR neurological pathogenesis. A miRNA microarray was used to identify differentially expr...
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/PMC6138635/ https://www.ncbi.nlm.nih.gov/pubmed/30217997 http://dx.doi.org/10.1038/s41598-018-32189-5 |
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author | Chen, Juncao Gong, Xiaoyun Huang, Li Chen, Pingyang Wang, Tao Zhou, Wei Luo, Kaiju Wang, Jing |
author_facet | Chen, Juncao Gong, Xiaoyun Huang, Li Chen, Pingyang Wang, Tao Zhou, Wei Luo, Kaiju Wang, Jing |
author_sort | Chen, Juncao |
collection | PubMed |
description | In humans, malnutrition during pregnancy results in intrauterine growth restriction (IUGR) and an increased risk of neurological morbidities; altered miRNA characteristics have been suggested to contribute to IUGR neurological pathogenesis. A miRNA microarray was used to identify differentially expressed miRNA molecules in the hippocampi of rats with IUGR. Five of the molecules in question were selectively validated using real-time PCR in rats with IUGR. We then investigated the role of miR-199a-5p in hippocampal pathology. Bioinformatics analysis results suggested that TNF-α, caspase-3 and SIRT1 were potential targets of miR-199a-5p. Changes in PI3K, SIRT1 and caspase-3 protein expressions levels in the hippocampus were confirmed by Western blot analysis (all P < 0.05). Studies using the pheochromocytoma cell line PC12 cells and primary neurons demonstrated that miR-199a-5p modulated PI3K, caspase-3 and SIRT1 expression. Additionally, there was an inverse correlation between miR-199a-5p and caspase-3 expression, though dual-luciferase reporter assays showed that caspase-3 is not a target of miR-199a-5p. We conclude that IUGR affects hippocampal miRNAs characteristics. Our results also indicated that aberrantly high expression levels of miR-199a-5p may play an important role in the pathogenesis of IUGR by regulating SIRT1 and PI3K. |
format | Online Article Text |
id | pubmed-6138635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61386352018-09-15 MiR-199a-5p regulates sirtuin1 and PI3K in the rat hippocampus with intrauterine growth restriction Chen, Juncao Gong, Xiaoyun Huang, Li Chen, Pingyang Wang, Tao Zhou, Wei Luo, Kaiju Wang, Jing Sci Rep Article In humans, malnutrition during pregnancy results in intrauterine growth restriction (IUGR) and an increased risk of neurological morbidities; altered miRNA characteristics have been suggested to contribute to IUGR neurological pathogenesis. A miRNA microarray was used to identify differentially expressed miRNA molecules in the hippocampi of rats with IUGR. Five of the molecules in question were selectively validated using real-time PCR in rats with IUGR. We then investigated the role of miR-199a-5p in hippocampal pathology. Bioinformatics analysis results suggested that TNF-α, caspase-3 and SIRT1 were potential targets of miR-199a-5p. Changes in PI3K, SIRT1 and caspase-3 protein expressions levels in the hippocampus were confirmed by Western blot analysis (all P < 0.05). Studies using the pheochromocytoma cell line PC12 cells and primary neurons demonstrated that miR-199a-5p modulated PI3K, caspase-3 and SIRT1 expression. Additionally, there was an inverse correlation between miR-199a-5p and caspase-3 expression, though dual-luciferase reporter assays showed that caspase-3 is not a target of miR-199a-5p. We conclude that IUGR affects hippocampal miRNAs characteristics. Our results also indicated that aberrantly high expression levels of miR-199a-5p may play an important role in the pathogenesis of IUGR by regulating SIRT1 and PI3K. Nature Publishing Group UK 2018-09-14 /pmc/articles/PMC6138635/ /pubmed/30217997 http://dx.doi.org/10.1038/s41598-018-32189-5 Text en © The Author(s) 2018 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 Chen, Juncao Gong, Xiaoyun Huang, Li Chen, Pingyang Wang, Tao Zhou, Wei Luo, Kaiju Wang, Jing MiR-199a-5p regulates sirtuin1 and PI3K in the rat hippocampus with intrauterine growth restriction |
title | MiR-199a-5p regulates sirtuin1 and PI3K in the rat hippocampus with intrauterine growth restriction |
title_full | MiR-199a-5p regulates sirtuin1 and PI3K in the rat hippocampus with intrauterine growth restriction |
title_fullStr | MiR-199a-5p regulates sirtuin1 and PI3K in the rat hippocampus with intrauterine growth restriction |
title_full_unstemmed | MiR-199a-5p regulates sirtuin1 and PI3K in the rat hippocampus with intrauterine growth restriction |
title_short | MiR-199a-5p regulates sirtuin1 and PI3K in the rat hippocampus with intrauterine growth restriction |
title_sort | mir-199a-5p regulates sirtuin1 and pi3k in the rat hippocampus with intrauterine growth restriction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138635/ https://www.ncbi.nlm.nih.gov/pubmed/30217997 http://dx.doi.org/10.1038/s41598-018-32189-5 |
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