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A progesterone-brown fat axis is involved in regulating fetal growth
Pregnancy is associated with profound maternal metabolic changes, necessary for the growth and development of the fetus, mediated by reproductive signals acting on metabolic organs. However, the role of brown adipose tissue (BAT) in regulating gestational metabolism is unknown. We show that BAT phen...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587669/ https://www.ncbi.nlm.nih.gov/pubmed/28878263 http://dx.doi.org/10.1038/s41598-017-10979-7 |
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author | McIlvride, Saraid Mushtaq, Aleena Papacleovoulou, Georgia Hurling, Chloe Steel, Jennifer Jansen, Eugène Abu-Hayyeh, Shadi Williamson, Catherine |
author_facet | McIlvride, Saraid Mushtaq, Aleena Papacleovoulou, Georgia Hurling, Chloe Steel, Jennifer Jansen, Eugène Abu-Hayyeh, Shadi Williamson, Catherine |
author_sort | McIlvride, Saraid |
collection | PubMed |
description | Pregnancy is associated with profound maternal metabolic changes, necessary for the growth and development of the fetus, mediated by reproductive signals acting on metabolic organs. However, the role of brown adipose tissue (BAT) in regulating gestational metabolism is unknown. We show that BAT phenotype is lost in murine pregnancy, while there is a gain of white adipose tissue (WAT)-like features. This is characterised by reduced thermogenic capacity and mitochondrial content, accompanied by increased levels of markers of WAT and lipid accumulation. Surgical ablation of BAT prior to conception caused maternal and fetal hyperlipidemia, and consequently larger fetuses. We show that BAT phenotype is altered from day 5 of gestation, implicating early pregnancy factors, which was confirmed by reduced expression of BAT markers in progesterone challenged oophorectomised mice. Moreover, in vitro data using primary BAT cultures show a direct impact of progesterone on expression of Ucp1. These data demonstrate that progesterone mediates a phenotypic change in BAT, which contributes to the gestational metabolic environment, and thus overall fetal size. |
format | Online Article Text |
id | pubmed-5587669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55876692017-09-13 A progesterone-brown fat axis is involved in regulating fetal growth McIlvride, Saraid Mushtaq, Aleena Papacleovoulou, Georgia Hurling, Chloe Steel, Jennifer Jansen, Eugène Abu-Hayyeh, Shadi Williamson, Catherine Sci Rep Article Pregnancy is associated with profound maternal metabolic changes, necessary for the growth and development of the fetus, mediated by reproductive signals acting on metabolic organs. However, the role of brown adipose tissue (BAT) in regulating gestational metabolism is unknown. We show that BAT phenotype is lost in murine pregnancy, while there is a gain of white adipose tissue (WAT)-like features. This is characterised by reduced thermogenic capacity and mitochondrial content, accompanied by increased levels of markers of WAT and lipid accumulation. Surgical ablation of BAT prior to conception caused maternal and fetal hyperlipidemia, and consequently larger fetuses. We show that BAT phenotype is altered from day 5 of gestation, implicating early pregnancy factors, which was confirmed by reduced expression of BAT markers in progesterone challenged oophorectomised mice. Moreover, in vitro data using primary BAT cultures show a direct impact of progesterone on expression of Ucp1. These data demonstrate that progesterone mediates a phenotypic change in BAT, which contributes to the gestational metabolic environment, and thus overall fetal size. Nature Publishing Group UK 2017-09-06 /pmc/articles/PMC5587669/ /pubmed/28878263 http://dx.doi.org/10.1038/s41598-017-10979-7 Text en © The Author(s) 2017 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 McIlvride, Saraid Mushtaq, Aleena Papacleovoulou, Georgia Hurling, Chloe Steel, Jennifer Jansen, Eugène Abu-Hayyeh, Shadi Williamson, Catherine A progesterone-brown fat axis is involved in regulating fetal growth |
title | A progesterone-brown fat axis is involved in regulating fetal growth |
title_full | A progesterone-brown fat axis is involved in regulating fetal growth |
title_fullStr | A progesterone-brown fat axis is involved in regulating fetal growth |
title_full_unstemmed | A progesterone-brown fat axis is involved in regulating fetal growth |
title_short | A progesterone-brown fat axis is involved in regulating fetal growth |
title_sort | progesterone-brown fat axis is involved in regulating fetal growth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587669/ https://www.ncbi.nlm.nih.gov/pubmed/28878263 http://dx.doi.org/10.1038/s41598-017-10979-7 |
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