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Polystyrene Nanoplastics Induce DNA Damage and Excitotoxicity in Whole-Brain Organoids: The Role of the TLR9/MyD88 Pathway

Toxics 2025 Score: 48 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Yizhe Wei, Gaofang Cao, Jianping Ma, Yanan Mi, Y. B. Zhao, Leili Zhang, Bingyan Wang, Huanliang Liu, Kang Li, Yue Shi, Yue Shi, Wenqing Lai, Wenqing Lai, Tian Li, Bencheng Lin

Summary

Researchers exposed whole-brain organoids—lab-grown 3D brain tissue models—to polystyrene nanoplastics and investigated neurotoxic mechanisms. The nanoplastics caused DNA damage and excitotoxicity through activation of the TLR9/MyD88 immune signaling pathway, identifying inflammatory receptor activation as a key mechanism by which nanoplastics trigger developmental neurotoxicity.

Polymers
Models
Study Type In vitro

Polystyrene nanoplastics (PS-NPs) can cross the placenta and blood-brain barrier to accumulate in the fetal brain following inhalation or ingestion, raising concerns about PS-NPs-induced developmental neurotoxicity (DNT). However, current evidence regarding the mechanisms underlying PS-NPs-elicited DNT remains critically scarce. Given the inherent limitations of two-dimensional cell culture techniques, we employed a whole-brain organoid (WBO) model, which more faithfully recapitulates the dynamic changes and substantial alterations during the early development of the human nervous system, to investigate the PS-NPs-induced DNT. Developing WBOs were exposed to 50-nm PS-NPs at concentrations of 50 and 100 μg/mL. Additionally, we established an early developmental exposure model in neonatal rat for robust validation. The results revealed aberrant formation of the tissue architecture of neural epithelial buds in PS-NPs-exposed WBOs, accompanied by significant inflammatory responses and oxidative stress. Marked DNA damage and substantial activation of the TLR9/MyD88 pathway were observed in WBOs and in the cerebral cortex of neonatal rat, leading to significant upregulation of the excitotoxicity marker c-Fos and the excitatory synaptic marker NMDAR. In vitro assays revealed that melatonin treatment could efficiently counteract PS-NPs-mediated neuronal impairment, with both the reduced cell viability and excessive DNA damage induced by PS-NPs being restored to levels close to those of the control group. In conclusion, by establishing WBOs and early developmental exposure models in neonatal rat, we found that PS-NPs can induce DNA double-strand breaks, and activation of the TLR9 pathway mediates PS-NPs-induced excitotoxicity.

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