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Mitochondria Associated MicroRNA Expression Profiling of Heart Failure
Heart failure (HF) is associated with mitochondrial dysfunction and energy metabolism impairment. MicroRNAs are implicated in the development of heart failure. However, the mitochondria enriched microRNA during heart failure remains elusive. Here, we generated a pressure overload-induced early and l...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632880/ https://www.ncbi.nlm.nih.gov/pubmed/29147650 http://dx.doi.org/10.1155/2017/4042509 |
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author | Wang, Xiaoxia Song, Chun Zhou, Xiao Han, Xiaorui Li, Jun Wang, Zengwu Shang, Haibao Liu, Yuli Cao, Huiqing |
author_facet | Wang, Xiaoxia Song, Chun Zhou, Xiao Han, Xiaorui Li, Jun Wang, Zengwu Shang, Haibao Liu, Yuli Cao, Huiqing |
author_sort | Wang, Xiaoxia |
collection | PubMed |
description | Heart failure (HF) is associated with mitochondrial dysfunction and energy metabolism impairment. MicroRNAs are implicated in the development of heart failure. However, the mitochondria enriched microRNA during heart failure remains elusive. Here, we generated a pressure overload-induced early and late stage heart failure model at 4 weeks and 8 weeks following transverse aortic constriction (TAC) in mice. We found that expression of mitochondrion protein COX4 was highly enriched in isolated mitochondria from cardiac tissues while GAPDH could hardly be detected. Furthermore, small RNA sequencing for mitochondria RNAs from failing hearts was performed. It was found that 69 microRNAs were upregulated and 2 were downregulated in early heart failure, while 16 microRNAs were upregulated and 6 were downregulated in late heart failure. 15 microRNA candidates were measured in both mitochondria and total cardiac tissues of heart failure by real-time PCR. MiR-696, miR-532, miR-690, and miR-345-3p were enriched in mitochondria from the failing heart at early stage. Bioinformatics analysis showed that mitochondria enriched microRNAs in HF were associated with energy metabolism and oxidative stress pathway. For the first time, we demonstrated microRNAs were enriched in mitochondria during heart failure, which established a link between microRNA and mitochondrion in heart failure. |
format | Online Article Text |
id | pubmed-5632880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-56328802017-11-16 Mitochondria Associated MicroRNA Expression Profiling of Heart Failure Wang, Xiaoxia Song, Chun Zhou, Xiao Han, Xiaorui Li, Jun Wang, Zengwu Shang, Haibao Liu, Yuli Cao, Huiqing Biomed Res Int Research Article Heart failure (HF) is associated with mitochondrial dysfunction and energy metabolism impairment. MicroRNAs are implicated in the development of heart failure. However, the mitochondria enriched microRNA during heart failure remains elusive. Here, we generated a pressure overload-induced early and late stage heart failure model at 4 weeks and 8 weeks following transverse aortic constriction (TAC) in mice. We found that expression of mitochondrion protein COX4 was highly enriched in isolated mitochondria from cardiac tissues while GAPDH could hardly be detected. Furthermore, small RNA sequencing for mitochondria RNAs from failing hearts was performed. It was found that 69 microRNAs were upregulated and 2 were downregulated in early heart failure, while 16 microRNAs were upregulated and 6 were downregulated in late heart failure. 15 microRNA candidates were measured in both mitochondria and total cardiac tissues of heart failure by real-time PCR. MiR-696, miR-532, miR-690, and miR-345-3p were enriched in mitochondria from the failing heart at early stage. Bioinformatics analysis showed that mitochondria enriched microRNAs in HF were associated with energy metabolism and oxidative stress pathway. For the first time, we demonstrated microRNAs were enriched in mitochondria during heart failure, which established a link between microRNA and mitochondrion in heart failure. Hindawi 2017 2017-09-24 /pmc/articles/PMC5632880/ /pubmed/29147650 http://dx.doi.org/10.1155/2017/4042509 Text en Copyright © 2017 Xiaoxia Wang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Xiaoxia Song, Chun Zhou, Xiao Han, Xiaorui Li, Jun Wang, Zengwu Shang, Haibao Liu, Yuli Cao, Huiqing Mitochondria Associated MicroRNA Expression Profiling of Heart Failure |
title | Mitochondria Associated MicroRNA Expression Profiling of Heart Failure |
title_full | Mitochondria Associated MicroRNA Expression Profiling of Heart Failure |
title_fullStr | Mitochondria Associated MicroRNA Expression Profiling of Heart Failure |
title_full_unstemmed | Mitochondria Associated MicroRNA Expression Profiling of Heart Failure |
title_short | Mitochondria Associated MicroRNA Expression Profiling of Heart Failure |
title_sort | mitochondria associated microrna expression profiling of heart failure |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5632880/ https://www.ncbi.nlm.nih.gov/pubmed/29147650 http://dx.doi.org/10.1155/2017/4042509 |
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