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Association of polybrominated diphenyl ether (PBDE) levels with biomarkers of placental development and disease during mid-gestation
BACKGROUND: Polybrominated diphenyl ether (PBDE) exposures have been associated with adverse pregnancy outcomes. A hypothesized mechanism is via alterations in placental development and function. However, we lack biomarkers that can be used as early indicators of maternal/fetal response to PBDE expo...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268484/ https://www.ncbi.nlm.nih.gov/pubmed/32493340 http://dx.doi.org/10.1186/s12940-020-00617-7 |
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author | Varshavsky, Julia R. Robinson, Joshua F. Zhou, Yan Puckett, Kenisha A. Kwan, Elaine Buarpung, Sirirak Aburajab, Rayyan Gaw, Stephanie L. Sen, Saunak Smith, Sabrina Crispo Frankenfield, Julie Park, June-Soo Fisher, Susan J. Woodruff, Tracey J. |
author_facet | Varshavsky, Julia R. Robinson, Joshua F. Zhou, Yan Puckett, Kenisha A. Kwan, Elaine Buarpung, Sirirak Aburajab, Rayyan Gaw, Stephanie L. Sen, Saunak Smith, Sabrina Crispo Frankenfield, Julie Park, June-Soo Fisher, Susan J. Woodruff, Tracey J. |
author_sort | Varshavsky, Julia R. |
collection | PubMed |
description | BACKGROUND: Polybrominated diphenyl ether (PBDE) exposures have been associated with adverse pregnancy outcomes. A hypothesized mechanism is via alterations in placental development and function. However, we lack biomarkers that can be used as early indicators of maternal/fetal response to PBDE exposures and/or perturbations in placental development or function. METHODS: To evaluate the relationship between PBDE levels and placental biomarkers during mid-gestation of human pregnancy (n = 62), we immunolocalized three molecules that play key roles in cytotrophoblast (CTB) differentiation and interstitial/endovascular uterine invasion—integrin alpha-1 (ITGA1), vascular endothelial-cadherin (CDH5), and metalloproteinase-1 (MMP1)–and assessed three morphological parameters as potential indicators of pathological alterations using H&E-stained tissues–leukocyte infiltration, fibrinoid deposition, and CTB endovascular invasion. We evaluated associations between placental PBDE levels and of biomarkers of placental development and disease using censored Kendall’s tau correlation and linear regression methods. RESULTS: PBDEs were detected in all placental samples. We observed substantial variation in antigen expression and morphological endpoints across placental regions. We observed an association between PBDE concentrations and immunoreactivity of endovascular CTB staining with anti-ITGA1 (inverse) or interstitial CTBs staining with anti-CDH5 (positive). CONCLUSIONS: We found several molecular markers that may be sensitive placental indicators of PBDE exposure. Further, this indicates that placental biomarkers of development and disease could be useful barometers of exposure to PBDEs, a paradigm that could be extended to other environmental chemicals and placental stage-specific antigens. |
format | Online Article Text |
id | pubmed-7268484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72684842020-06-07 Association of polybrominated diphenyl ether (PBDE) levels with biomarkers of placental development and disease during mid-gestation Varshavsky, Julia R. Robinson, Joshua F. Zhou, Yan Puckett, Kenisha A. Kwan, Elaine Buarpung, Sirirak Aburajab, Rayyan Gaw, Stephanie L. Sen, Saunak Smith, Sabrina Crispo Frankenfield, Julie Park, June-Soo Fisher, Susan J. Woodruff, Tracey J. Environ Health Research BACKGROUND: Polybrominated diphenyl ether (PBDE) exposures have been associated with adverse pregnancy outcomes. A hypothesized mechanism is via alterations in placental development and function. However, we lack biomarkers that can be used as early indicators of maternal/fetal response to PBDE exposures and/or perturbations in placental development or function. METHODS: To evaluate the relationship between PBDE levels and placental biomarkers during mid-gestation of human pregnancy (n = 62), we immunolocalized three molecules that play key roles in cytotrophoblast (CTB) differentiation and interstitial/endovascular uterine invasion—integrin alpha-1 (ITGA1), vascular endothelial-cadherin (CDH5), and metalloproteinase-1 (MMP1)–and assessed three morphological parameters as potential indicators of pathological alterations using H&E-stained tissues–leukocyte infiltration, fibrinoid deposition, and CTB endovascular invasion. We evaluated associations between placental PBDE levels and of biomarkers of placental development and disease using censored Kendall’s tau correlation and linear regression methods. RESULTS: PBDEs were detected in all placental samples. We observed substantial variation in antigen expression and morphological endpoints across placental regions. We observed an association between PBDE concentrations and immunoreactivity of endovascular CTB staining with anti-ITGA1 (inverse) or interstitial CTBs staining with anti-CDH5 (positive). CONCLUSIONS: We found several molecular markers that may be sensitive placental indicators of PBDE exposure. Further, this indicates that placental biomarkers of development and disease could be useful barometers of exposure to PBDEs, a paradigm that could be extended to other environmental chemicals and placental stage-specific antigens. BioMed Central 2020-06-03 /pmc/articles/PMC7268484/ /pubmed/32493340 http://dx.doi.org/10.1186/s12940-020-00617-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Varshavsky, Julia R. Robinson, Joshua F. Zhou, Yan Puckett, Kenisha A. Kwan, Elaine Buarpung, Sirirak Aburajab, Rayyan Gaw, Stephanie L. Sen, Saunak Smith, Sabrina Crispo Frankenfield, Julie Park, June-Soo Fisher, Susan J. Woodruff, Tracey J. Association of polybrominated diphenyl ether (PBDE) levels with biomarkers of placental development and disease during mid-gestation |
title | Association of polybrominated diphenyl ether (PBDE) levels with biomarkers of placental development and disease during mid-gestation |
title_full | Association of polybrominated diphenyl ether (PBDE) levels with biomarkers of placental development and disease during mid-gestation |
title_fullStr | Association of polybrominated diphenyl ether (PBDE) levels with biomarkers of placental development and disease during mid-gestation |
title_full_unstemmed | Association of polybrominated diphenyl ether (PBDE) levels with biomarkers of placental development and disease during mid-gestation |
title_short | Association of polybrominated diphenyl ether (PBDE) levels with biomarkers of placental development and disease during mid-gestation |
title_sort | association of polybrominated diphenyl ether (pbde) levels with biomarkers of placental development and disease during mid-gestation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268484/ https://www.ncbi.nlm.nih.gov/pubmed/32493340 http://dx.doi.org/10.1186/s12940-020-00617-7 |
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