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Investigation of potential toxic effects of nano- and microplastics on human endometrial stromal cells

Reproductive Toxicology 2025 6 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 63 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Inha Lee, Nara Kim, Nara Kim, Nara Kim, Nara Kim, Joo Hyun Park, Inha Lee, Jae Hoon Lee, Joo Hyun Park, Joo Hyun Park, Jae Hoon Lee, Jae Hoon Lee, Gee Soo Jung, Inha Lee, Inha Lee, Gee Soo Jung, Inha Lee, Joo Hyun Park, Inha Lee, Young Sik Choi Young Sik Choi Nara Kim, Gee Soo Jung, Gee Soo Jung, Gee Soo Jung, Gee Soo Jung, Gee Soo Jung, Jae Hoon Lee, SiHyun Cho, SiHyun Cho, Jae Hoon Lee, Jae Hoon Lee, Gee Soo Jung, Min Jung Lee, Min Jung Lee, Min Jung Lee, Wooseok Im, Wooseok Im, Wooseok Im, Wooseok Im, SiHyun Cho, SiHyun Cho, SiHyun Cho, SiHyun Cho, Young Sik Choi Young Sik Choi

Summary

Researchers exposed human endometrial cells (uterine lining cells) to polystyrene nano- and microplastics and found that smaller particles (100 nanometers) were taken up most readily, accumulating in both the nucleus and cytoplasm. At higher concentrations, the nanoplastics reduced cell growth and triggered cell death. These findings suggest that nanoplastics could pose a risk to uterine health and potentially affect fertility and pregnancy outcomes.

Polymers
Study Type In vitro

Nanoplastics (NPs) and microplastics (MPs) have become a global concern in recent years. Most current research on the impact of plastics on obstetrics has focused on their accumulation in specific tissues in animal models and the disease-causing potential of MPs. However, there is a relative lack of research on the cellular changes caused by the accumulation of MPs. In this study, we aimed to establish a proper in vitro exposure protocol for polystyrene (PS)-NPs and MPs and to investigate possible cytotoxic effects of PS-NPs and MPs on human endometrial stromal cells (ESCs) using different plastic sizes and concentrations. The results showed that smaller plastics, specifically 100 nm PS-NPs and 1 μm PS-MPs, had a higher cellular uptake propensity than larger particles, such as 5 μm PS-MPs, with significant morphological changes and cell death observed at concentrations above 100 μg/mL a 24-h period. In addition, confocal microscopy and real-time imaging confirmed the accumulation of these particles in the nucleus and cytoplasm, with internalization rates correlating with particle size. Also, 100 nm PS-NPs reduced cell proliferation and induced apoptosis. In conclusion, this study demonstrates that exposure to 100 nm PS-NPs and 1 μm PS-MPs leads to dynamic accumulation in ESCs, resulting in cell death or decreased proliferation at specific concentrations, which highlights the potential cellular toxicity of NPs or MPs.

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