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Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort

BACKGROUND: Air pollution exposure during pregnancy has been associated with adverse birth outcomes and health problems later in life. We investigated sex-specific transcriptomic responses to gestational long- and short-term exposure to particulate matter with a diameter < 2.5 μm (PM(2.5)) in ord...

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Autores principales: Winckelmans, Ellen, Vrijens, Karen, Tsamou, Maria, Janssen, Bram G., Saenen, Nelly D., Roels, Harry A., Kleinjans, Jos, Lefebvre, Wouter, Vanpoucke, Charlotte, de Kok, Theo M., Nawrot, Tim S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458481/
https://www.ncbi.nlm.nih.gov/pubmed/28583124
http://dx.doi.org/10.1186/s12940-017-0264-y
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author Winckelmans, Ellen
Vrijens, Karen
Tsamou, Maria
Janssen, Bram G.
Saenen, Nelly D.
Roels, Harry A.
Kleinjans, Jos
Lefebvre, Wouter
Vanpoucke, Charlotte
de Kok, Theo M.
Nawrot, Tim S.
author_facet Winckelmans, Ellen
Vrijens, Karen
Tsamou, Maria
Janssen, Bram G.
Saenen, Nelly D.
Roels, Harry A.
Kleinjans, Jos
Lefebvre, Wouter
Vanpoucke, Charlotte
de Kok, Theo M.
Nawrot, Tim S.
author_sort Winckelmans, Ellen
collection PubMed
description BACKGROUND: Air pollution exposure during pregnancy has been associated with adverse birth outcomes and health problems later in life. We investigated sex-specific transcriptomic responses to gestational long- and short-term exposure to particulate matter with a diameter < 2.5 μm (PM(2.5)) in order to elucidate potential underlying mechanisms of action. METHODS: Whole genome gene expression was investigated in cord blood of 142 mother-newborn pairs that were enrolled in the ENVIRONAGE birth cohort. Daily PM(2.5) exposure levels were calculated for each mother’s home address using a spatial-temporal interpolation model in combination with a dispersion model to estimate both long- (annual average before delivery) and short- (last month of pregnancy) term exposure. We explored the association between gene expression levels and PM(2.5) exposure, and identified modulated pathways by overrepresentation analysis and gene set enrichment analysis. RESULTS: Some processes were altered in both sexes for long- (e.g. DNA damage) or short-term exposure (e.g. olfactory signaling). For long-term exposure in boys neurodevelopment and RhoA pathways were modulated, while in girls defensin expression was down-regulated. For short-term exposure we identified pathways related to synaptic transmission and mitochondrial function (boys) and immune response (girls). CONCLUSIONS: This is the first whole genome gene expression study in cord blood to identify sex-specific pathways altered by PM(2.5). The identified transcriptome pathways could provide new molecular insights as to the interaction pattern of early life PM(2.5) exposure with the biological development of the fetus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12940-017-0264-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-54584812017-06-07 Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort Winckelmans, Ellen Vrijens, Karen Tsamou, Maria Janssen, Bram G. Saenen, Nelly D. Roels, Harry A. Kleinjans, Jos Lefebvre, Wouter Vanpoucke, Charlotte de Kok, Theo M. Nawrot, Tim S. Environ Health Research BACKGROUND: Air pollution exposure during pregnancy has been associated with adverse birth outcomes and health problems later in life. We investigated sex-specific transcriptomic responses to gestational long- and short-term exposure to particulate matter with a diameter < 2.5 μm (PM(2.5)) in order to elucidate potential underlying mechanisms of action. METHODS: Whole genome gene expression was investigated in cord blood of 142 mother-newborn pairs that were enrolled in the ENVIRONAGE birth cohort. Daily PM(2.5) exposure levels were calculated for each mother’s home address using a spatial-temporal interpolation model in combination with a dispersion model to estimate both long- (annual average before delivery) and short- (last month of pregnancy) term exposure. We explored the association between gene expression levels and PM(2.5) exposure, and identified modulated pathways by overrepresentation analysis and gene set enrichment analysis. RESULTS: Some processes were altered in both sexes for long- (e.g. DNA damage) or short-term exposure (e.g. olfactory signaling). For long-term exposure in boys neurodevelopment and RhoA pathways were modulated, while in girls defensin expression was down-regulated. For short-term exposure we identified pathways related to synaptic transmission and mitochondrial function (boys) and immune response (girls). CONCLUSIONS: This is the first whole genome gene expression study in cord blood to identify sex-specific pathways altered by PM(2.5). The identified transcriptome pathways could provide new molecular insights as to the interaction pattern of early life PM(2.5) exposure with the biological development of the fetus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12940-017-0264-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-05 /pmc/articles/PMC5458481/ /pubmed/28583124 http://dx.doi.org/10.1186/s12940-017-0264-y Text en © The Author(s). 2017 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
Winckelmans, Ellen
Vrijens, Karen
Tsamou, Maria
Janssen, Bram G.
Saenen, Nelly D.
Roels, Harry A.
Kleinjans, Jos
Lefebvre, Wouter
Vanpoucke, Charlotte
de Kok, Theo M.
Nawrot, Tim S.
Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort
title Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort
title_full Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort
title_fullStr Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort
title_full_unstemmed Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort
title_short Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort
title_sort newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the environage birth cohort
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458481/
https://www.ncbi.nlm.nih.gov/pubmed/28583124
http://dx.doi.org/10.1186/s12940-017-0264-y
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