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Label-free detection of uptake, accumulation, and translocation of diesel exhaust particles in ex vivo perfused human placenta

Background Pregnant women and developing fetuses comprise a particularly vulnerable population as multiple studies have shown associations between prenatal air pollution exposure and adverse pregnancy outcomes. However, the mechanisms underlying the observed developmental toxicity are mostly unknown...

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Published in:Journal of Nanobiotechnology 2021, Vol.19 (1)
Main Authors: Bongaerts, Eva, Aengenheister, Leonie, Dugershaw, Battuja B, Manser, Pius, Roeffaers, Maarten B. J, Ameloot, Marcel, Nawrot, Tim S, Bové, Hannelore, Buerki-Thurnherr, Tina
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container_title Journal of Nanobiotechnology
container_volume 19
creator Bongaerts, Eva
Aengenheister, Leonie
Dugershaw, Battuja B
Manser, Pius
Roeffaers, Maarten B. J
Ameloot, Marcel
Nawrot, Tim S
Bové, Hannelore
Buerki-Thurnherr, Tina
description Background Pregnant women and developing fetuses comprise a particularly vulnerable population as multiple studies have shown associations between prenatal air pollution exposure and adverse pregnancy outcomes. However, the mechanisms underlying the observed developmental toxicity are mostly unknown, in particular, if pollution particles can cross the human placenta to reach the fetal circulation. Results Here, we investigated the accumulation and translocation of diesel exhaust particles (DEPs), as a model particle for combustion-derived pollution, in human perfused placentae using label-free detection by femtosecond pulsed laser illumination. The results do not reveal a significant particle transfer across term placentae within 6 h of perfusion. However, DEPs accumulate in placental tissue, especially in the syncytiotrophoblast layer that mediates a wealth of essential functions to support and maintain a successful pregnancy. Furthermore, DEPs are found in placental macrophages and fetal endothelial cells, showing that some particles can overcome the syncytiotrophoblasts to reach the fetal capillaries. Few particles are also observed inside fetal microvessels. Conclusions Overall, we show that DEPs accumulate in key cell types of the placental tissue and can cross the human placenta, although in limited amounts. These findings are crucial for risk assessment and protection of pregnant women and highlight the urgent need for further research on the direct and indirect placenta-mediated developmental toxicity of ambient particulates. Keywords: Environmental pollution, Diesel exhaust particles, In utero exposure, Ex vivo placental perfusion, Nanosafety
doi_str_mv 10.1186/s12951-021-00886-5
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J ; Ameloot, Marcel ; Nawrot, Tim S ; Bové, Hannelore ; Buerki-Thurnherr, Tina</creator><creatorcontrib>Bongaerts, Eva ; Aengenheister, Leonie ; Dugershaw, Battuja B ; Manser, Pius ; Roeffaers, Maarten B. J ; Ameloot, Marcel ; Nawrot, Tim S ; Bové, Hannelore ; Buerki-Thurnherr, Tina</creatorcontrib><description>Background Pregnant women and developing fetuses comprise a particularly vulnerable population as multiple studies have shown associations between prenatal air pollution exposure and adverse pregnancy outcomes. However, the mechanisms underlying the observed developmental toxicity are mostly unknown, in particular, if pollution particles can cross the human placenta to reach the fetal circulation. Results Here, we investigated the accumulation and translocation of diesel exhaust particles (DEPs), as a model particle for combustion-derived pollution, in human perfused placentae using label-free detection by femtosecond pulsed laser illumination. The results do not reveal a significant particle transfer across term placentae within 6 h of perfusion. However, DEPs accumulate in placental tissue, especially in the syncytiotrophoblast layer that mediates a wealth of essential functions to support and maintain a successful pregnancy. Furthermore, DEPs are found in placental macrophages and fetal endothelial cells, showing that some particles can overcome the syncytiotrophoblasts to reach the fetal capillaries. Few particles are also observed inside fetal microvessels. Conclusions Overall, we show that DEPs accumulate in key cell types of the placental tissue and can cross the human placenta, although in limited amounts. These findings are crucial for risk assessment and protection of pregnant women and highlight the urgent need for further research on the direct and indirect placenta-mediated developmental toxicity of ambient particulates. 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Results Here, we investigated the accumulation and translocation of diesel exhaust particles (DEPs), as a model particle for combustion-derived pollution, in human perfused placentae using label-free detection by femtosecond pulsed laser illumination. The results do not reveal a significant particle transfer across term placentae within 6 h of perfusion. However, DEPs accumulate in placental tissue, especially in the syncytiotrophoblast layer that mediates a wealth of essential functions to support and maintain a successful pregnancy. Furthermore, DEPs are found in placental macrophages and fetal endothelial cells, showing that some particles can overcome the syncytiotrophoblasts to reach the fetal capillaries. Few particles are also observed inside fetal microvessels. Conclusions Overall, we show that DEPs accumulate in key cell types of the placental tissue and can cross the human placenta, although in limited amounts. These findings are crucial for risk assessment and protection of pregnant women and highlight the urgent need for further research on the direct and indirect placenta-mediated developmental toxicity of ambient particulates. 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source Publicly Available Content (ProQuest); PubMed Central
subjects Air pollution
Analysis
Diesel motor exhaust gas
Health aspects
title Label-free detection of uptake, accumulation, and translocation of diesel exhaust particles in ex vivo perfused human placenta
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