Cargando…

BPA-Induced Deregulation Of Epigenetic Patterns: Effects On Female Zebrafish Reproduction

Bisphenol A (BPA) is one of the commonest Endocrine Disruptor Compounds worldwide. It interferes with vertebrate reproduction, possibly by inducing deregulation of epigenetic mechanisms. To determine its effects on female reproductive physiology and investigate whether changes in the expression leve...

Descripción completa

Detalles Bibliográficos
Autores principales: Santangeli, Stefania, Maradonna, Francesca, Gioacchini, Giorgia, Cobellis, Gilda, Piccinetti, Chiara Carla, Dalla Valle, Luisa, Carnevali, Oliana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766405/
https://www.ncbi.nlm.nih.gov/pubmed/26911650
http://dx.doi.org/10.1038/srep21982
_version_ 1782417660299968512
author Santangeli, Stefania
Maradonna, Francesca
Gioacchini, Giorgia
Cobellis, Gilda
Piccinetti, Chiara Carla
Dalla Valle, Luisa
Carnevali, Oliana
author_facet Santangeli, Stefania
Maradonna, Francesca
Gioacchini, Giorgia
Cobellis, Gilda
Piccinetti, Chiara Carla
Dalla Valle, Luisa
Carnevali, Oliana
author_sort Santangeli, Stefania
collection PubMed
description Bisphenol A (BPA) is one of the commonest Endocrine Disruptor Compounds worldwide. It interferes with vertebrate reproduction, possibly by inducing deregulation of epigenetic mechanisms. To determine its effects on female reproductive physiology and investigate whether changes in the expression levels of genes related to reproduction are caused by histone modifications, BPA concentrations consistent with environmental exposure were administered to zebrafish for three weeks. Effects on oocyte growth and maturation, autophagy and apoptosis processes, histone modifications, and DNA methylation were assessed by Real-Time PCR (qPCR), histology, and chromatin immunoprecipitation combined with qPCR analysis (ChIP-qPCR). The results showed that 5 μg/L BPA down-regulated oocyte maturation-promoting signals, likely through changes in the chromatin structure mediated by histone modifications, and promoted apoptosis in mature follicles. These data indicate that the negative effects of BPA on the female reproductive system may be due to its upstream ability to deregulate epigenetic mechanism.
format Online
Article
Text
id pubmed-4766405
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-47664052016-03-02 BPA-Induced Deregulation Of Epigenetic Patterns: Effects On Female Zebrafish Reproduction Santangeli, Stefania Maradonna, Francesca Gioacchini, Giorgia Cobellis, Gilda Piccinetti, Chiara Carla Dalla Valle, Luisa Carnevali, Oliana Sci Rep Article Bisphenol A (BPA) is one of the commonest Endocrine Disruptor Compounds worldwide. It interferes with vertebrate reproduction, possibly by inducing deregulation of epigenetic mechanisms. To determine its effects on female reproductive physiology and investigate whether changes in the expression levels of genes related to reproduction are caused by histone modifications, BPA concentrations consistent with environmental exposure were administered to zebrafish for three weeks. Effects on oocyte growth and maturation, autophagy and apoptosis processes, histone modifications, and DNA methylation were assessed by Real-Time PCR (qPCR), histology, and chromatin immunoprecipitation combined with qPCR analysis (ChIP-qPCR). The results showed that 5 μg/L BPA down-regulated oocyte maturation-promoting signals, likely through changes in the chromatin structure mediated by histone modifications, and promoted apoptosis in mature follicles. These data indicate that the negative effects of BPA on the female reproductive system may be due to its upstream ability to deregulate epigenetic mechanism. Nature Publishing Group 2016-02-25 /pmc/articles/PMC4766405/ /pubmed/26911650 http://dx.doi.org/10.1038/srep21982 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Santangeli, Stefania
Maradonna, Francesca
Gioacchini, Giorgia
Cobellis, Gilda
Piccinetti, Chiara Carla
Dalla Valle, Luisa
Carnevali, Oliana
BPA-Induced Deregulation Of Epigenetic Patterns: Effects On Female Zebrafish Reproduction
title BPA-Induced Deregulation Of Epigenetic Patterns: Effects On Female Zebrafish Reproduction
title_full BPA-Induced Deregulation Of Epigenetic Patterns: Effects On Female Zebrafish Reproduction
title_fullStr BPA-Induced Deregulation Of Epigenetic Patterns: Effects On Female Zebrafish Reproduction
title_full_unstemmed BPA-Induced Deregulation Of Epigenetic Patterns: Effects On Female Zebrafish Reproduction
title_short BPA-Induced Deregulation Of Epigenetic Patterns: Effects On Female Zebrafish Reproduction
title_sort bpa-induced deregulation of epigenetic patterns: effects on female zebrafish reproduction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766405/
https://www.ncbi.nlm.nih.gov/pubmed/26911650
http://dx.doi.org/10.1038/srep21982
work_keys_str_mv AT santangelistefania bpainducedderegulationofepigeneticpatternseffectsonfemalezebrafishreproduction
AT maradonnafrancesca bpainducedderegulationofepigeneticpatternseffectsonfemalezebrafishreproduction
AT gioacchinigiorgia bpainducedderegulationofepigeneticpatternseffectsonfemalezebrafishreproduction
AT cobellisgilda bpainducedderegulationofepigeneticpatternseffectsonfemalezebrafishreproduction
AT piccinettichiaracarla bpainducedderegulationofepigeneticpatternseffectsonfemalezebrafishreproduction
AT dallavalleluisa bpainducedderegulationofepigeneticpatternseffectsonfemalezebrafishreproduction
AT carnevalioliana bpainducedderegulationofepigeneticpatternseffectsonfemalezebrafishreproduction