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In vitro exposure to polystyrene microplastics exerts oocyte toxicity through cumulus cells damage in the sheep model

Frontiers in Veterinary Science 2026 Score: 50 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Letizia Temerario, Antonella Mastrorocco, Maria Carmela Ferrante Letizia Temerario, Andrea Podda, Luisa Bogliolo, Antonella Mastrorocco, Maria Carmela Ferrante Nicola Antonio Martino, Maria Carmela Ferrante Pierfrancesco Pinto, Pierfrancesco Pinto, Maria Elena Dell’Aquila, Maria Elena Dell’Aquila, Maria Carmela Ferrante Nicola Antonio Martino, Maria Carmela Ferrante Maria Carmela Ferrante Maria Carmela Ferrante Maria Carmela Ferrante Maria Carmela Ferrante Maria Carmela Ferrante Maria Carmela Ferrante Maria Carmela Ferrante Maria Carmela Ferrante

Summary

Scientists exposed sheep egg cells to tiny plastic particles called microplastics and found that higher amounts damaged the cells that support egg development, leading to lower-quality eggs. The plastic particles caused harmful stress and cell death in these support cells, which then prevented the eggs from developing properly. This research suggests that microplastics in our environment could potentially harm fertility by interfering with how eggs mature, though more studies are needed to confirm effects in humans.

Polymers
Body Systems
Study Type In vitro

Introduction In recent years, the widespread environmental presence of microplastics (MPs) has raised major concerns regarding animal and human health, including potential risks to reproductive function and offspring. Methods This study aimed to evaluate the effects of increasing concentrations of polystyrene MPs (PS-MPs; 0, 5, 50, or 100 μg/mL) on ovine cumulus–oocyte complexes (COCs) during in vitro maturation (IVM). Fluorescent microspheres were used for uptake assessment into COCs and cumulus cells (CCs) monolayers, whereas non-fluorescent PS-MPs were employed to evaluate potential toxic effects induced on CCs and oocytes. Results As regards CCs, increased PS-MPs uptake was highlighted at the highest exposure concentration (100 μg/mL), whereas no significant differences were observed in oocyte intracellular fluorescence intensity, compared to the control. The bioaccumulation increment in CCs monolayers was already visible after 6 h, both at 5 and 100 μg/mL, and confirmed at 24 h. The real-time PCR analysis in CCs revealed significant reductions in the expression levels of genes involved in antioxidant defense and alterations in those implicated in apoptosis. Finally, the TUNEL assay revealed a dose-dependent increase in CCs apoptotic index. Consequently, PS-MPs exposure impaired oocyte meiosis resumption by significantly reducing the maturation rates, particularly at 50 and 100 μg/mL, whereas no effects were observed at 5 μg/mL. Oocyte intracellular reactive oxygen species levels were significantly increased at all concentrations, whereas no differences in mitochondrial membrane potential were detected. The percentages of oocytes with abnormal configurations of meiotic spindle and cortical F-actin were found to be significantly increased, regardless of concentration. Finally, the cleavage rate was significantly reduced in oocytes exposed to 50 μg/mL, whereas no differences were found in the blastocyst rate at both 50 and 5 μg/mL. Discussion In conclusion, in vitro exposure of sheep COCs to PS-MPs during IVM reduced oocyte quality and developmental potential through alterations induced in the CCs, which turned out to be the main target of these environmental contaminants.

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