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Photoaging of polystyrene-based microplastics amplifies inflammatory response in macrophages

Chemosphere 2024 15 citations

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Researchers found that polystyrene microplastics aged by sunlight exposure for just three hours triggered stronger inflammatory responses and DNA damage in immune cells than fresh microplastics, even at very low concentrations. The aging process changed the particles' surface properties, making them more biologically reactive. Since most microplastics in the real world have been weathered by sunlight, this study suggests their actual health impact may be greater than lab studies using pristine particles indicate.

Polymers
Body Systems
Models

The continuous release of municipal and industrial products into the environment poses a growing concern for public health. Among environmental pollutants, polystyrene (PS) stands out as a primary constituent of environmental plastic waste, given its widespread use and high production rates owing to its durability and user-friendly properties. The detection of polystyrene microparticles (PS-MPs) in various living organisms has been well-documented, posing a serious threat due to their potential passage into the human ecosystem. In this manuscript, we aimed to study the toxicological effects of low concentrations of pristine and photoaged PS-MPs in a murine macrophage cell line. To this purpose, PS-MPs were photoaged by indoor exposure to visible light to simulate environmental weathering due to solar irradiation (PS-MPs3h). Physical characterization revealed that the irradiation treatment results in particle degradation and the possible release of nanoparticles. Monocultures of the RAW264.7 cell line were then exposed to PS-MPs and PS-MPs3h at concentrations comparable to experimental measurements from biological samples, to assess cytotoxicity, intracellular oxidative stress, primary genotoxicity, and inflammatory effects. Significant toxicity-related outcomes were observed in cells treated with both pristine PS-MPs and PS-MPs3h even at low concentrations (0,10 μg/ml and 1 μg/ml). PS-MPs3h exhibited greater adverse effects compared to PS-MPs, including reduced cell viability, increased ROS production, elevated DNA damage, and upregulation of IL-6 and NOS2 gene expression. Therefore, we can conclude that changes induced by environmental aging in the physicochemical composition of PS microplastics play a crucial role in the adverse health outcomes associated with microplastic exposure.

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When plastic waste breaks down in sunlight, it doesn't just become smaller pieces, it actually changes chemically in ways that can make it more toxic to cells, according to this review of existing research. Scientists found that sun-damaged microplastics and nanoplastics are often more harmful to cells than fresh, unweathered plastic particles, though how harmful depends on the plastic type and other conditions. This matters because most plastic pollution in the environment has been sitting in the sun for a while, so real-world exposure may pose greater health risks than lab studies using pristine plastic particles suggest.

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New insights into the size-independent bioactive potential of pristine and UV-B aged polyethylene microplastics

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Scientists tested how UV light aging changes polyethylene microplastics and their effects on human immune cells (lymphocytes) from blood samples. Both new and UV-aged microplastics reduced cell viability and triggered DNA damage, regardless of particle size. This suggests that microplastics in the environment may harm human immune cells whether they are freshly produced or have been weathered by sunlight.

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