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Maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome

BACKGROUND: The integration of engineered nanomaterials (ENM) is well-established and widespread in clinical, commercial, and domestic applications. Cardiovascular dysfunctions have been reported in adult populations after exposure to a variety of ENM. As the diversity of these exposures continues t...

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Autores principales: Stapleton, P. A., Hathaway, Q. A., Nichols, C. E., Abukabda, A. B., Pinti, M. V., Shepherd, D. L., McBride, C. R., Yi, J., Castranova, V. C., Hollander, J. M., Nurkiewicz, T. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763571/
https://www.ncbi.nlm.nih.gov/pubmed/29321036
http://dx.doi.org/10.1186/s12989-017-0239-8
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author Stapleton, P. A.
Hathaway, Q. A.
Nichols, C. E.
Abukabda, A. B.
Pinti, M. V.
Shepherd, D. L.
McBride, C. R.
Yi, J.
Castranova, V. C.
Hollander, J. M.
Nurkiewicz, T. R.
author_facet Stapleton, P. A.
Hathaway, Q. A.
Nichols, C. E.
Abukabda, A. B.
Pinti, M. V.
Shepherd, D. L.
McBride, C. R.
Yi, J.
Castranova, V. C.
Hollander, J. M.
Nurkiewicz, T. R.
author_sort Stapleton, P. A.
collection PubMed
description BACKGROUND: The integration of engineered nanomaterials (ENM) is well-established and widespread in clinical, commercial, and domestic applications. Cardiovascular dysfunctions have been reported in adult populations after exposure to a variety of ENM. As the diversity of these exposures continues to increase, the fetal ramifications of maternal exposures have yet to be determined. We, and others, have explored the consequences of ENM inhalation during gestation and identified many cardiovascular and metabolic outcomes in the F1 generation. The purpose of these studies was to identify genetic alterations in the F1 generation of Sprague-Dawley rats that result from maternal ENM inhalation during gestation. Pregnant dams were exposed to nano-titanium dioxide (nano-TiO(2)) aerosols (10 ± 0.5 mg/m(3)) for 7-8 days (calculated, cumulative lung deposition = 217 ± 1 μg) and on GD (gestational day) 20 fetal hearts were isolated. DNA was extracted and immunoprecipitated with modified chromatin marks histone 3 lysine 4 tri-methylation (H3K4me3) and histone 3 lysine 27 tri-methylation (H3K27me3). Following chromatin immunoprecipitation (ChIP), DNA fragments were sequenced. RNA from fetal hearts was purified and prepared for RNA sequencing and transcriptomic analysis. Ingenuity Pathway Analysis (IPA) was then used to identify pathways most modified by gestational ENM exposure. RESULTS: The results of the sequencing experiments provide initial evidence that significant epigenetic and transcriptomic changes occur in the cardiac tissue of maternal nano-TiO(2) exposed progeny. The most notable alterations in major biologic systems included immune adaptation and organismal growth. Changes in normal physiology were linked with other tissues, including liver and kidneys. CONCLUSIONS: These results are the first evidence that maternal ENM inhalation impacts the fetal epigenome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12989-017-0239-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-57635712018-01-17 Maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome Stapleton, P. A. Hathaway, Q. A. Nichols, C. E. Abukabda, A. B. Pinti, M. V. Shepherd, D. L. McBride, C. R. Yi, J. Castranova, V. C. Hollander, J. M. Nurkiewicz, T. R. Part Fibre Toxicol Research BACKGROUND: The integration of engineered nanomaterials (ENM) is well-established and widespread in clinical, commercial, and domestic applications. Cardiovascular dysfunctions have been reported in adult populations after exposure to a variety of ENM. As the diversity of these exposures continues to increase, the fetal ramifications of maternal exposures have yet to be determined. We, and others, have explored the consequences of ENM inhalation during gestation and identified many cardiovascular and metabolic outcomes in the F1 generation. The purpose of these studies was to identify genetic alterations in the F1 generation of Sprague-Dawley rats that result from maternal ENM inhalation during gestation. Pregnant dams were exposed to nano-titanium dioxide (nano-TiO(2)) aerosols (10 ± 0.5 mg/m(3)) for 7-8 days (calculated, cumulative lung deposition = 217 ± 1 μg) and on GD (gestational day) 20 fetal hearts were isolated. DNA was extracted and immunoprecipitated with modified chromatin marks histone 3 lysine 4 tri-methylation (H3K4me3) and histone 3 lysine 27 tri-methylation (H3K27me3). Following chromatin immunoprecipitation (ChIP), DNA fragments were sequenced. RNA from fetal hearts was purified and prepared for RNA sequencing and transcriptomic analysis. Ingenuity Pathway Analysis (IPA) was then used to identify pathways most modified by gestational ENM exposure. RESULTS: The results of the sequencing experiments provide initial evidence that significant epigenetic and transcriptomic changes occur in the cardiac tissue of maternal nano-TiO(2) exposed progeny. The most notable alterations in major biologic systems included immune adaptation and organismal growth. Changes in normal physiology were linked with other tissues, including liver and kidneys. CONCLUSIONS: These results are the first evidence that maternal ENM inhalation impacts the fetal epigenome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12989-017-0239-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-10 /pmc/articles/PMC5763571/ /pubmed/29321036 http://dx.doi.org/10.1186/s12989-017-0239-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Stapleton, P. A.
Hathaway, Q. A.
Nichols, C. E.
Abukabda, A. B.
Pinti, M. V.
Shepherd, D. L.
McBride, C. R.
Yi, J.
Castranova, V. C.
Hollander, J. M.
Nurkiewicz, T. R.
Maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome
title Maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome
title_full Maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome
title_fullStr Maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome
title_full_unstemmed Maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome
title_short Maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome
title_sort maternal engineered nanomaterial inhalation during gestation alters the fetal transcriptome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763571/
https://www.ncbi.nlm.nih.gov/pubmed/29321036
http://dx.doi.org/10.1186/s12989-017-0239-8
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