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Anionic nanoplastic exposure induces endothelial leakiness
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Researchers discovered that nanoplastics made of anionic polystyrene and poly(methyl methacrylate) can disrupt the junctions between blood vessel cells, causing increased vascular leakiness. This effect was dose-dependent and driven by biophysical interactions rather than typical cell toxicity like oxidative stress or cell death. The findings reveal a previously unknown way that nanoplastics could affect the body's circulatory system by making blood vessels more permeable.
The global-scale production of plastics has been instrumental in advancing modern society, while the rising accumulation of plastics in landfills, oceans, and anything in between has become a major stressor on environmental sustainability, climate, and, potentially, human health. While mechanical and chemical forces of man and nature can eventually break down or recycle plastics, our understanding of the biological fingerprints of plastics, especially of nanoplastics, remains poor. Here we report on a phenomenon associated with the nanoplastic forms of anionic polystyrene and poly(methyl methacrylate), where their introduction disrupted the vascular endothelial cadherin junctions in a dose-dependent manner, as revealed by confocal fluorescence microscopy, signaling pathways, molecular dynamics simulations, as well as ex vivo and in vivo assays with animal model systems. Collectively, our results implicated nanoplastics-induced vasculature permeability as primarily biophysical-biochemical in nature, uncorrelated with cytotoxic events such as reactive oxygen species production, autophagy, and apoptosis. This uncovered route of paracellular transport has opened up vast avenues for investigating the behaviour and biological effects of nanoplastics, which may offer crucial insights for guiding innovations towards a sustainable plastics industry and environmental remediation.
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Nanoplastic-induced vascular endothelial injury and coagulation dysfunction in mice
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Researchers exposed mice to polystyrene nanoplastics with different surface modifications and found that the particles caused structural damage to vascular endothelial cells and triggered inflammatory responses. The nanoplastics also disrupted blood coagulation function in the mice. The study suggests that nanoplastic exposure may pose risks to cardiovascular health due to the particles' ability to travel through the bloodstream and damage blood vessel linings.
Polystyrene Nanoplastics Perturb Cell Membranes and Induce Bystander Uptake of Diverse Cargos
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Tiny plastic particles from everyday pollution can physically damage cell membranes, making cells "leaky." This lets other harmful substances, like toxic proteins or metals, sneak into cells more easily, meaning nanoplastics may worsen the toxic effects of other pollutants we're exposed to, not just cause harm on their own.
Effects of micro- and nanoplastics on blood cells in vitro and cardiovascular parameters in vivo, considering their presence in the human bloodstream and potential impact on blood pressure
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This review examines evidence that micro- and nanoplastics can enter the human bloodstream and interact with blood cells, with plastic particles already detected in human blood, blood clots, and artery plaques. While direct evidence linking microplastics to blood pressure changes in humans is still lacking, animal studies and the mechanisms identified -- including blood vessel damage and inflammation -- suggest cardiovascular effects are plausible.
Polystyrene nanoplastic-encapsulated extracellular vesicles promote blood-brain barrier breakdown and accumulate in the brain.
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Researchers found that extracellular vesicles encapsulating polystyrene nanoplastics prolonged intracellular retention in human endothelial cells, caused a 2.8-fold greater decline in blood-brain barrier electrical resistance than free nanoplastics alone, and promoted brain accumulation in vivo — implicating vesicle-mediated transport as a significant route for nanoplastic neurological entry.
Cell-nanoplastics association impacts cell proliferation and motility
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Researchers used microfluidic-calibrated fluorescence microscopy to quantify nanoplastic accumulation across epithelial, endothelial, fibroblast, and immune cell types at concentrations matching human tissue measurements, finding that nanoplastics broadly impaired cell proliferation and reduced motility in T cells and fibroblasts, with polystyrene, polyethylene, and polypropylene showing similar toxicity but markedly different cellular uptake and release dynamics.
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