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Weathered plastic particles negatively affect mouse primary neurons and glial cells

Archives of Toxicology 2026 Score: 50 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Hyun Seung Shin, Yun Hee So, David Lee, Yunsoo Chang, Minjung Kim, DongJoo Joung, BuHyun Youn, Eun-Hee Lee, Eui-Man Jung

Summary

Scientists tested how tiny plastic particles affect brain cells from mice and found that weathered plastics (those broken down by sunlight and wear) are more harmful than fresh plastic particles. The weathered plastic pieces killed more brain cells, caused more inflammation, and reduced cell growth compared to new plastic particles. This matters because weathered plastic particles are everywhere in our environment, and this study suggests they could potentially harm brain health more than we previously thought.

The global increase in plastics production has raised significant concerns regarding plastic waste in marine and terrestrial ecosystems and potential human health risks. Environmental weathering processes such as physical abrasion and ultraviolet (UV) irradiation cause plastic waste to fragment into tiny particles termed weathered nano- and microplastics (W-NMPs). Despite their potential human health hazards, W-NMPs are underinvestigated in terms of their effects, particularly on the central nervous system. We comparatively evaluated the effects of W-NMPs and plain NMPs (P-NMPs) synthesized for specific purposes on brain-derived cells in vitro. W-NMPs triggered apoptosis more robustly than P-NMPs in both primary neural progenitors and isolated oligodendrocyte progenitors, and significantly reduced cell proliferation in primary neural progenitors. We found that W-NMPs induced a more potent inflammatory response in isolated primary microglia than P-NMPs. In the neuron-glia co-culture model, W-NMPs also caused morphological changes in astrocytes. Finally, P-NMPs induced microglial cytotoxicity, but W-NMPs triggered a more vigorous inflammatory response in microglia than P-NMPs in the co-culture model. Our findings provide novel insights into the hazards of W-NMPs exposure to brain health.

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