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A Systems Biology Approach to Investigating Sex Differences in Cardiac Hypertrophy
BACKGROUND: Heart failure preceded by hypertrophy is a leading cause of death, and sex differences in hypertrophy are well known, although the basis for these sex differences is poorly understood. METHODS AND RESULTS: This study used a systems biology approach to investigate mechanisms underlying se...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5586433/ https://www.ncbi.nlm.nih.gov/pubmed/28862954 http://dx.doi.org/10.1161/JAHA.117.005838 |
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author | Harrington, Josephine Fillmore, Natasha Gao, Shouguo Yang, Yanqin Zhang, Xue Liu, Poching Stoehr, Andrea Chen, Ye Springer, Danielle Zhu, Jun Wang, Xujing Murphy, Elizabeth |
author_facet | Harrington, Josephine Fillmore, Natasha Gao, Shouguo Yang, Yanqin Zhang, Xue Liu, Poching Stoehr, Andrea Chen, Ye Springer, Danielle Zhu, Jun Wang, Xujing Murphy, Elizabeth |
author_sort | Harrington, Josephine |
collection | PubMed |
description | BACKGROUND: Heart failure preceded by hypertrophy is a leading cause of death, and sex differences in hypertrophy are well known, although the basis for these sex differences is poorly understood. METHODS AND RESULTS: This study used a systems biology approach to investigate mechanisms underlying sex differences in cardiac hypertrophy. Male and female mice were treated for 2 and 3 weeks with angiotensin II to induce hypertrophy. Sex differences in cardiac hypertrophy were apparent after 3 weeks of treatment. RNA sequencing was performed on hearts, and sex differences in mRNA expression at baseline and following hypertrophy were observed, as well as within‐sex differences between baseline and hypertrophy. Sex differences in mRNA were substantial at baseline and reduced somewhat with hypertrophy, as the mRNA differences induced by hypertrophy tended to overwhelm the sex differences. We performed an integrative analysis to identify mRNA networks that were differentially regulated in the 2 sexes by hypertrophy and obtained a network centered on PPARα (peroxisome proliferator‐activated receptor α). Mouse experiments further showed that acute inhibition of PPARα blocked sex differences in the development of hypertrophy. CONCLUSIONS: The data in this study suggest that PPARα is involved in the sex‐dimorphic regulation of cardiac hypertrophy. |
format | Online Article Text |
id | pubmed-5586433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55864332017-09-11 A Systems Biology Approach to Investigating Sex Differences in Cardiac Hypertrophy Harrington, Josephine Fillmore, Natasha Gao, Shouguo Yang, Yanqin Zhang, Xue Liu, Poching Stoehr, Andrea Chen, Ye Springer, Danielle Zhu, Jun Wang, Xujing Murphy, Elizabeth J Am Heart Assoc Original Research BACKGROUND: Heart failure preceded by hypertrophy is a leading cause of death, and sex differences in hypertrophy are well known, although the basis for these sex differences is poorly understood. METHODS AND RESULTS: This study used a systems biology approach to investigate mechanisms underlying sex differences in cardiac hypertrophy. Male and female mice were treated for 2 and 3 weeks with angiotensin II to induce hypertrophy. Sex differences in cardiac hypertrophy were apparent after 3 weeks of treatment. RNA sequencing was performed on hearts, and sex differences in mRNA expression at baseline and following hypertrophy were observed, as well as within‐sex differences between baseline and hypertrophy. Sex differences in mRNA were substantial at baseline and reduced somewhat with hypertrophy, as the mRNA differences induced by hypertrophy tended to overwhelm the sex differences. We performed an integrative analysis to identify mRNA networks that were differentially regulated in the 2 sexes by hypertrophy and obtained a network centered on PPARα (peroxisome proliferator‐activated receptor α). Mouse experiments further showed that acute inhibition of PPARα blocked sex differences in the development of hypertrophy. CONCLUSIONS: The data in this study suggest that PPARα is involved in the sex‐dimorphic regulation of cardiac hypertrophy. John Wiley and Sons Inc. 2017-08-19 /pmc/articles/PMC5586433/ /pubmed/28862954 http://dx.doi.org/10.1161/JAHA.117.005838 Text en © 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Harrington, Josephine Fillmore, Natasha Gao, Shouguo Yang, Yanqin Zhang, Xue Liu, Poching Stoehr, Andrea Chen, Ye Springer, Danielle Zhu, Jun Wang, Xujing Murphy, Elizabeth A Systems Biology Approach to Investigating Sex Differences in Cardiac Hypertrophy |
title | A Systems Biology Approach to Investigating Sex Differences in Cardiac Hypertrophy |
title_full | A Systems Biology Approach to Investigating Sex Differences in Cardiac Hypertrophy |
title_fullStr | A Systems Biology Approach to Investigating Sex Differences in Cardiac Hypertrophy |
title_full_unstemmed | A Systems Biology Approach to Investigating Sex Differences in Cardiac Hypertrophy |
title_short | A Systems Biology Approach to Investigating Sex Differences in Cardiac Hypertrophy |
title_sort | systems biology approach to investigating sex differences in cardiac hypertrophy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5586433/ https://www.ncbi.nlm.nih.gov/pubmed/28862954 http://dx.doi.org/10.1161/JAHA.117.005838 |
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