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Large-sized polystyrene microplastics induce oxidative stress in AML12 cells

Scientific Reports 2025 4 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Bowen Zhao, Rui Liu, Shu-Hao Guo, Yiran Li, Zekai Huang, Yihan Wang, Cuiping Yu, Zhijun Hou, Yuanyuan Zhang, Yanlong Zhang, Xuedong Liu

Summary

Researchers exposed mouse liver cells to large polystyrene microplastics (50 micrometers) and found that even these bigger particles caused significant oxidative stress. Amino-modified microplastics were particularly harmful, triggering higher levels of reactive oxygen species and cell damage than unmodified particles. The study expands understanding of microplastic toxicity beyond the well-studied nanoscale range, showing that larger particles can also harm cells.

Polymers
Body Systems
Models

Microplastics (MPs), particularly those exceeding 20 μm in diameter, are increasingly detected in environment and animal tissues, yet their cytotoxicity remains poorly understood. While existing studies focused on MPs with relatively small sizes (≤ 20 μm) or nanoplastics (NPs), the biological impacts of large-sized MPs and amino-modified MPs are underexplored. In this study, we investigated the oxidative stress (OS)-mediated responses of alpha mouse liver 12 (AML12) cells to 50 μm polystyrene MPs (PS-MPs) and polystyrene-amine modified MPs (PS-NH-MPs) at concentrations of 0, 0.05, 0.1, 0.2, and 0.5 mg/mL for a duration of 48 h. Our investigation particularly emphasised on responses of apoptosis and ferroptosis. Intriguingly, exposure to PS-MPs at concentrations below 0.5 mg/mL did not induce significant ferroptosis-related alterations. However, at 0.5 mg/mL, PS-MPs triggered a significant increase in intracellular reactive oxygen species and reduced cell viability, paralleled by upregulated Caspase-9 mRNA expression, suggesting OS-driven apoptotic priming. Notably, surface functionalization with PS-NH-MPs did not amplify these effects compared to pristine PS-MPs, indicating particle size dominate hepatocyte responses. These findings provide a toxicological paradigm for large-sized MPs, emphasising OS as a pivotal evaluation criterion for risk assessment. These results provide a novel perspective for environmental monitoring of MPs.

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