Cargando…

Differential susceptibility to endocrine disruptor-induced epimutagenesis

There is now considerable evidence indicating the potential for endocrine disrupting chemicals to alter the epigenome and for subsets of these epigenomic changes or “epimutations” to be heritably transmitted to offspring in subsequent generations. While there have been many studies indicating how ex...

Descripción completa

Detalles Bibliográficos
Autores principales: Lehle, Jake D, McCarrey, John R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722801/
https://www.ncbi.nlm.nih.gov/pubmed/33324495
http://dx.doi.org/10.1093/eep/dvaa016
_version_ 1783620223507628032
author Lehle, Jake D
McCarrey, John R
author_facet Lehle, Jake D
McCarrey, John R
author_sort Lehle, Jake D
collection PubMed
description There is now considerable evidence indicating the potential for endocrine disrupting chemicals to alter the epigenome and for subsets of these epigenomic changes or “epimutations” to be heritably transmitted to offspring in subsequent generations. While there have been many studies indicating how exposure to endocrine disrupting chemicals can disrupt various organs associated with the body’s endocrine systems, there is relatively limited information regarding the relative susceptibility of different specific organs, tissues, or cell types to endocrine disrupting chemical-induced epimutagenesis. Here we review available information about different organs, tissues, cell types, and/or cell lines which have been shown to be susceptible to specific endocrine disrupting chemical-induced epimutations. In addition, we discuss possible mechanisms that may be involved, or impacted by this tissue- or cell type-specific, differential susceptibility to different endocrine disrupting chemicals. Finally, we summarize available information indicating that certain periods of development display elevated susceptibility to endocrine disrupting chemical exposure and we describe how this may affect the extent to which germline epimutations can be transmitted inter- or transgenerationally. We conclude that cell type-specific differential susceptibility to endocrine disrupting chemical-induced epimutagenesis is likely to directly impact the extent to, or manner in, which endocrine disrupting chemical exposure initially induces epigenetic changes to DNA methylation and/or histone modifications, and how these endocrine disrupting chemical-induced epimutations can then subsequently impact gene expression, potentially leading to the development of heritable disease states.
format Online
Article
Text
id pubmed-7722801
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77228012020-12-14 Differential susceptibility to endocrine disruptor-induced epimutagenesis Lehle, Jake D McCarrey, John R Environ Epigenet Review Article There is now considerable evidence indicating the potential for endocrine disrupting chemicals to alter the epigenome and for subsets of these epigenomic changes or “epimutations” to be heritably transmitted to offspring in subsequent generations. While there have been many studies indicating how exposure to endocrine disrupting chemicals can disrupt various organs associated with the body’s endocrine systems, there is relatively limited information regarding the relative susceptibility of different specific organs, tissues, or cell types to endocrine disrupting chemical-induced epimutagenesis. Here we review available information about different organs, tissues, cell types, and/or cell lines which have been shown to be susceptible to specific endocrine disrupting chemical-induced epimutations. In addition, we discuss possible mechanisms that may be involved, or impacted by this tissue- or cell type-specific, differential susceptibility to different endocrine disrupting chemicals. Finally, we summarize available information indicating that certain periods of development display elevated susceptibility to endocrine disrupting chemical exposure and we describe how this may affect the extent to which germline epimutations can be transmitted inter- or transgenerationally. We conclude that cell type-specific differential susceptibility to endocrine disrupting chemical-induced epimutagenesis is likely to directly impact the extent to, or manner in, which endocrine disrupting chemical exposure initially induces epigenetic changes to DNA methylation and/or histone modifications, and how these endocrine disrupting chemical-induced epimutations can then subsequently impact gene expression, potentially leading to the development of heritable disease states. Oxford University Press 2020-12-08 /pmc/articles/PMC7722801/ /pubmed/33324495 http://dx.doi.org/10.1093/eep/dvaa016 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Review Article
Lehle, Jake D
McCarrey, John R
Differential susceptibility to endocrine disruptor-induced epimutagenesis
title Differential susceptibility to endocrine disruptor-induced epimutagenesis
title_full Differential susceptibility to endocrine disruptor-induced epimutagenesis
title_fullStr Differential susceptibility to endocrine disruptor-induced epimutagenesis
title_full_unstemmed Differential susceptibility to endocrine disruptor-induced epimutagenesis
title_short Differential susceptibility to endocrine disruptor-induced epimutagenesis
title_sort differential susceptibility to endocrine disruptor-induced epimutagenesis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722801/
https://www.ncbi.nlm.nih.gov/pubmed/33324495
http://dx.doi.org/10.1093/eep/dvaa016
work_keys_str_mv AT lehlejaked differentialsusceptibilitytoendocrinedisruptorinducedepimutagenesis
AT mccarreyjohnr differentialsusceptibilitytoendocrinedisruptorinducedepimutagenesis