Environmental Toxicant Exposure Paralyzes Human Placental Macrophage Responses to Microbial Threat

Exposure to environmental toxicants (such as dioxins) has been epidemiologically linked to adverse reproductive health outcomes, including placental inflammation and preterm birth. However, the molecular underpinnings that govern these outcomes in gravid reproductive tissues remain largely unclear....

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Published inACS infectious diseases Vol. 9; no. 12; pp. 2401 - 2408
Main Authors Stephens, Victoria R, Moore, Rebecca E, Spicer, Sabrina K, Talbert, Julie A, Lu, Jacky, Chinni, Riya, Chambers, Schuyler A, Townsend, Steven D, Manning, Shannon D, Rogers, Lisa M, Aronoff, David M, Vue, Zer, Neikirk, Kit, Hinton, Jr, Antentor O, Damo, Steven M, Noble, Kristen N, Eastman, Alison J, McCallister, Monique M, Osteen, Kevin G, Gaddy, Jennifer A
Format Journal Article
LanguageEnglish
Published United States 08.12.2023
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Summary:Exposure to environmental toxicants (such as dioxins) has been epidemiologically linked to adverse reproductive health outcomes, including placental inflammation and preterm birth. However, the molecular underpinnings that govern these outcomes in gravid reproductive tissues remain largely unclear. Placental macrophages (also known as Hofbauer cells) are crucial innate immune cells that defend the gravid reproductive tract and help promote maternal-fetal tolerance. We hypothesized that exposure to environmental toxicants such as 2,3,7,8-tetrachlorodibenzo- -dioxin (TCDD) could alter placental macrophage responses to inflammatory insults such as infection. To test this, placental macrophages were cultured in the presence or absence of TCDD and then infected with the perinatal pathogen Group B (GBS). Our results indicate that TCDD is lethal to placental macrophages at and above a 5 nM concentration and that sublethal dioxin exposure inhibits phagocytosis and cytokine production. Taken together, these results indicate that TCDD paralyzes placental macrophage responses to bacterial infection.
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ISSN:2373-8227
2373-8227
DOI:10.1021/acsinfecdis.3c00490