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Cytotoxicity of Polystyrene Nanoplastics Involves Mitochondrial Dysfunction and DNA Damage in Hemocytes of the Pacific Oyster

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Scientists found that tiny plastic particles (nanoplastics) can damage the immune cells of oysters by harming their mitochondria, the "batteries" that power cells, leading to DNA damage even at low exposure levels. While this study was done in oysters, not humans, it adds to growing evidence that nanoplastics can disrupt basic cell functions, raising questions about what similar exposure might mean for human health given how widespread plastic pollution has become in our food and water.

Nanoplastics represent an increasing ecological threat to marine ecosystems, with the potential to disrupt immune responses, oxidative stress pathways, and bioenergetics. We employed an in vitro cellular bioassay to investigate the distribution, metabolic disruption, and genotoxicity resulting from 24 hours of exposure to polystyrene nanoplastics (NanoPS, approximately 90 nm) in the hemocytes of the Pacific oyster (Crassostrea gigas). Transmission electron microscopy suggested the internalization and distribution of NanoPS within vesicles, the cytosol, and the nuclei of exposed hemocytes. Cytotoxicity assays revealed that metabolic activity (resazurin assay, LC50 = 91.6 mg/L) was more sensitive than lysosomal integrity (neutral red assay, LC50 = 252.3 mg/L). Exposure to NanoPS also increased the levels of reactive oxygen species and DNA damage as low as 1.2 mg/L. Metabolic assays revealed that enhancing mitochondrial metabolism through galactose supplementation increased the cytotoxicity and DNA damage caused by NanoPS. Conversely, promoting anaerobic metabolism with glucose supplementation reduced these effects. Co-exposures with the mitochondrial uncoupler FCCP did not decrease cellular viability but elevated DNA damage. We suggest that mitochondria are a sensitive target of nanoplastics in bivalve hemocytes, highlighting the importance of considering aerobic metabolism in assessing nanoplastic toxicity. The strong correlation with the published in vivo effects of this same NanoPS highlights the biological relevance of this cellular toxicity assessment. This research supports the use of hemocyte-based cellular assays to complement in vivo studies for characterizing nanoplastic toxicity mechanisms in marine organisms.

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Cytotoxicity of polystyrene nanoplastics involves mitochondrial dysfunction and DNA damage in hemocytes of the Pacific oyster

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Researchers used an in vitro cellular bioassay with Pacific oyster hemocytes to investigate the toxicity of polystyrene nanoplastics, finding that 24-hour exposure caused mitochondrial dysfunction, elevated reactive oxygen species, and DNA damage. The results identify immune cell mitochondria as key targets of nanoplastic cytotoxicity in marine bivalves.

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Cellular Uptake and Nuclear Accumulation of Polystyrene Nanoplastics in 3T3 Fibroblasts and Hepatocytes of Rattus norvegicus

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