Bisphenol A disrupts apolipoprotein E expression through estrogen-related receptor gamma and DNA methlylation in the liver of male rare minnow Gobiocypris rarus

An increasing number of studies show that bisphenol A (BPA) can cause lipid metabolism disorder. However, few studies focused on the effect of BPA on lipid transport. Apolipoprotein E (ApoE) plays important roles in triglyceride (TG) transportation. Our previous study found that ApoE was a sensitive...

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Autores principales: Yingying Zhang, Zhu Zhu, Qiao Liu, Meng Zhang, Hui Yang, Wenzhi Wei
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/cd04d64e5af14d61843ecfef588218b4
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spelling oai:doaj.org-article:cd04d64e5af14d61843ecfef588218b42021-12-04T04:32:03ZBisphenol A disrupts apolipoprotein E expression through estrogen-related receptor gamma and DNA methlylation in the liver of male rare minnow Gobiocypris rarus0147-651310.1016/j.ecoenv.2021.113041https://doaj.org/article/cd04d64e5af14d61843ecfef588218b42021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S0147651321011532https://doaj.org/toc/0147-6513An increasing number of studies show that bisphenol A (BPA) can cause lipid metabolism disorder. However, few studies focused on the effect of BPA on lipid transport. Apolipoprotein E (ApoE) plays important roles in triglyceride (TG) transportation. Our previous study found that ApoE was a sensitive gene in response to BPA exposure in male rare minnow. To investigate the effect and mechanism of BPA on hepatic ApoE, adult male rare minnow Gobiocypris rarus were exposed to environmentally relevant concentrations of BPA (15 μg/L) for 1, 3 and 5 weeks. Results showed that BPA inhibited ApoE expression at week 1 and 5, while induced its expression at week 3. A positive estrogen-related receptor gamma (Esrrg) response element was identified in the promoter region of ApoE. The change of the Esrrg recruitment was consistent with ApoE mRNA expression. Moreover, the methylation status of the CpG sites near and on the Esrrg binding sites changed opposite to the ApoE mRNA level, which may be the main cause for the change in Esrrg recruitment. The expression of ApoE protein was significantly enhanced following long-term BPA exposure. Consistently, the TG accumulation was significantly increased in the plasma. The present study demonstrates that BPA could affect rare minnow ApoE expression, which is probably one of the ways for BPA disturbing fish lipid metabolism.Yingying ZhangZhu ZhuQiao LiuMeng ZhangHui YangWenzhi WeiElsevierarticleBisphenol ALipid metabolismApolipoprotein ELiverTriglycerideEnvironmental pollutionTD172-193.5Environmental sciencesGE1-350ENEcotoxicology and Environmental Safety, Vol 228, Iss , Pp 113041- (2021)
institution DOAJ
collection DOAJ
language EN
topic Bisphenol A
Lipid metabolism
Apolipoprotein E
Liver
Triglyceride
Environmental pollution
TD172-193.5
Environmental sciences
GE1-350
spellingShingle Bisphenol A
Lipid metabolism
Apolipoprotein E
Liver
Triglyceride
Environmental pollution
TD172-193.5
Environmental sciences
GE1-350
Yingying Zhang
Zhu Zhu
Qiao Liu
Meng Zhang
Hui Yang
Wenzhi Wei
Bisphenol A disrupts apolipoprotein E expression through estrogen-related receptor gamma and DNA methlylation in the liver of male rare minnow Gobiocypris rarus
description An increasing number of studies show that bisphenol A (BPA) can cause lipid metabolism disorder. However, few studies focused on the effect of BPA on lipid transport. Apolipoprotein E (ApoE) plays important roles in triglyceride (TG) transportation. Our previous study found that ApoE was a sensitive gene in response to BPA exposure in male rare minnow. To investigate the effect and mechanism of BPA on hepatic ApoE, adult male rare minnow Gobiocypris rarus were exposed to environmentally relevant concentrations of BPA (15 μg/L) for 1, 3 and 5 weeks. Results showed that BPA inhibited ApoE expression at week 1 and 5, while induced its expression at week 3. A positive estrogen-related receptor gamma (Esrrg) response element was identified in the promoter region of ApoE. The change of the Esrrg recruitment was consistent with ApoE mRNA expression. Moreover, the methylation status of the CpG sites near and on the Esrrg binding sites changed opposite to the ApoE mRNA level, which may be the main cause for the change in Esrrg recruitment. The expression of ApoE protein was significantly enhanced following long-term BPA exposure. Consistently, the TG accumulation was significantly increased in the plasma. The present study demonstrates that BPA could affect rare minnow ApoE expression, which is probably one of the ways for BPA disturbing fish lipid metabolism.
format article
author Yingying Zhang
Zhu Zhu
Qiao Liu
Meng Zhang
Hui Yang
Wenzhi Wei
author_facet Yingying Zhang
Zhu Zhu
Qiao Liu
Meng Zhang
Hui Yang
Wenzhi Wei
author_sort Yingying Zhang
title Bisphenol A disrupts apolipoprotein E expression through estrogen-related receptor gamma and DNA methlylation in the liver of male rare minnow Gobiocypris rarus
title_short Bisphenol A disrupts apolipoprotein E expression through estrogen-related receptor gamma and DNA methlylation in the liver of male rare minnow Gobiocypris rarus
title_full Bisphenol A disrupts apolipoprotein E expression through estrogen-related receptor gamma and DNA methlylation in the liver of male rare minnow Gobiocypris rarus
title_fullStr Bisphenol A disrupts apolipoprotein E expression through estrogen-related receptor gamma and DNA methlylation in the liver of male rare minnow Gobiocypris rarus
title_full_unstemmed Bisphenol A disrupts apolipoprotein E expression through estrogen-related receptor gamma and DNA methlylation in the liver of male rare minnow Gobiocypris rarus
title_sort bisphenol a disrupts apolipoprotein e expression through estrogen-related receptor gamma and dna methlylation in the liver of male rare minnow gobiocypris rarus
publisher Elsevier
publishDate 2021
url https://doaj.org/article/cd04d64e5af14d61843ecfef588218b4
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