Effects of co-exposure to benzo-a-pyrene and cerium dioxide nanoparticles on human lung and placental barriers

• Pollutant toxicity differs between co-exposure by parallel addition and BaP-coated CeO 2 NPs. • CYP1A1 induction by BaP-coated CeO 2 NPs is dose-dependent. • BaP adsorption onto CeO 2 NPs enhances CYP1A1 induction in bronchial cells. • Particle-bound pollutants should be considered in airborne toxicity assessments. Cerium dioxide nanoparticles (CeO 2 NPs) are emerging pollutants widely used for their catalytic properties in diesel fuel and cigarettes. Human exposure to CeO 2 NPs rarely occurs in isolation. Benzo-a-pyrene (BaP), a polycyclic aromatic hydrocarbon co-emitted from diesel engines, tends to adsorb onto CeO 2 NPs in contaminated environments. To better understand their combined effects on both the lung and placental tissues which are critical-barriers for the fetus, we coated CeO 2 NPs with BaP at two different ratios, mimicking environmental exposure. We characterized the physicochemical properties of BaP-coated NPs in bronchial and placental culture media, assessed coating stability and BaP desorption. We evaluated the biological impact of BaP-coated CeO 2 NPs on primary normal human bronchial epithelial cells and purified villous cytotrophoblasts from term human placentas. We compared the response of BaP-coated NPs with that observed under parallel co-exposure, and to individual exposures to BaP and CeO 2 NPs. Bronchial cells exhibited toxicity at lower doses under co-exposure by parallel addition compared to BaP-coated NPs. Cytochrome P450 (CYP1A1) induction varied between tissue barriers, exhibiting a BaP dose-dependent in both tissue models but coating-independent response in trophoblasts, whereas bronchial cells showed a stronger response to BaP adsorbed on CeO₂ NPs. These findings highlight how BaP, when stably associated with CeO 2 NPs, exerts modulated effects depending on the tissue, potentially altering its metabolic kinetics and thus its biopersistence. This study underscores the importance of considering particle-bound pollutants when evaluating the health impact of airborne particulate matter, as this more accurately reflects environmental exposure.

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Publication Details

Journal
Journal of Hazardous Materials Advances
Published
2025-06-27
DOI
https://doi.org/10.1016/j.hazadv.2025.100802
Citations
1
Primary Topic
Air Quality and Health Impacts
Type
article
Field-Weighted Citation Impact
1.20

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article

Effects of co-exposure to benzo-a-pyrene and cerium dioxide nanoparticles on human lung and placental barriers

Linh‐Chi Bui, Justine Renault, Gaëlle Deval, Charlotte Izabelle et al.
1 citations
Journal of Hazardous Materials Advances
Air Quality and Health Impacts
1.20
article

Effects of co-exposure to benzo-a-pyrene and cerium dioxide nanoparticles on human lung and placental barriers

Linh‐Chi Bui, Justine Renault, Gaëlle Deval, Charlotte Izabelle, Thierry Fournier, Ioana Ferecatu, Claire Mikolajczak, Sonja Boland, Didier Borderie, Stéphanie Devineau, Grégory Lefèvre, Safaa Mawas
article en
1 citations

Abstract

• Pollutant toxicity differs between co-exposure by parallel addition and BaP-coated CeO 2 NPs. • CYP1A1 induction by BaP-coated CeO 2 NPs is dose-dependent. • BaP adsorption onto CeO 2 NPs enhances CYP1A1 induction in bronchial cells. • Particle-bound pollutants should be considered in airborne toxicity assessments. Cerium dioxide nanoparticles (CeO 2 NPs) are emerging pollutants widely used for their catalytic properties in diesel fuel and cigarettes. Human exposure to CeO 2 NPs rarely occurs in isolation. Benzo-a-pyrene (BaP), a polycyclic aromatic hydrocarbon co-emitted from diesel engines, tends to adsorb onto CeO 2 NPs in contaminated environments. To better understand their combined effects on both the lung and placental tissues which are critical-barriers for the fetus, we coated CeO 2 NPs with BaP at two different ratios, mimicking environmental exposure. We characterized the physicochemical properties of BaP-coated NPs in bronchial and placental culture media, assessed coating stability and BaP desorption. We evaluated the biological impact of BaP-coated CeO 2 NPs on primary normal human bronchial epithelial cells and purified villous cytotrophoblasts from term human placentas. We compared the response of BaP-coated NPs with that observed under parallel co-exposure, and to individual exposures to BaP and CeO 2 NPs. Bronchial cells exhibited toxicity at lower doses under co-exposure by parallel addition compared to BaP-coated NPs. Cytochrome P450 (CYP1A1) induction varied between tissue barriers, exhibiting a BaP dose-dependent in both tissue models but coating-independent response in trophoblasts, whereas bronchial cells showed a stronger response to BaP adsorbed on CeO₂ NPs. These findings highlight how BaP, when stably associated with CeO 2 NPs, exerts modulated effects depending on the tissue, potentially altering its metabolic kinetics and thus its biopersistence. This study underscores the importance of considering particle-bound pollutants when evaluating the health impact of airborne particulate matter, as this more accurately reflects environmental exposure.

Journal of Hazardous Materials AdvancesVol. 19
Centre National de la Recherche Scientifique (FR), Inserm (FR), Université Paris Cité (FR), Université Paris Sciences et Lettres (FR), Hôpital Cochin (FR), Assistance Publique – Hôpitaux de Paris (FR), Institut de Recherche de Chimie Paris (FR), Unit of Functional and Adaptive Biology (FR)
Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Agence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du Travail
Openalex Percentile: Top 21%
Air Quality and Health Impacts
1.20
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