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Article Tier 2 Nanoplastics Reproductive & Development Sign in to save

Limited passage and functional effects of polystyrene micro- and nanoplastics in a physiologically-relevant in vitro human placental co-culture model

Reproductive Toxicology 2025 1 citation

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Researchers developed a placental co-culture model to study how polystyrene micro- and nanoplastics cross the placental barrier. The study found that smaller nanoplastics (50 nm) crossed more readily than larger particles, and while most cellular functions remained unaffected, exposure to the smallest nanoplastics caused a 17% decrease in estradiol hormone levels, suggesting potential endocrine effects.

Polymers
Body Systems
Study Type In vitro

The placenta plays a crucial role during pregnancy, yet effective in vitro models for placental toxicity testing are limited. In this study, a Transwell co-culture model combining BeWo b30 and HUVEC cells was developed and characterized, and used to study the transport and effects of polystyrene micro- and nanoplastics (PS-MNPs). After 72 h, 8.7 % of 50 nm and 1.2 % of 200 nm of fluorescent (F)PS-MNPs were detected on the basolateral side, while 1000 nm FPS-MNPs were undetectable. Confocal microscopy showed the uptake of 50 and 200 nm FPS-MNPs by the BeWo b30 and HUVEC cell layer, whereas the 1000 nm FPS-MNPs were only found within the BeWo b30 cell layer. Exposure to PS-MNPs (sizes of 50, 200 and 1000 nm at concentrations of 1-10 µg/mL) did not result in an effect on mitochondrial activity, oxidative stress and gene expression of several functional markers and steroidogenic enzymes. However, LC/MS-MS analysis of the culture media showed a decrease of 17 % in the level of 17-alpha-estradiol after 72-hour exposure to 1 µg/mL 50 nm PS-MNPs compared to vehicle control. Overall, our data showed limited effects of PS-MNPs on placental cell function in vitro, but FPS-MNPs were internalized and detected on the basolateral side in the co-culture. This warrants further studies on effects of MNPs on placental cell function, and particularly steroidogenesis, to assess the potential effects of MNPs during pregnancy.

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