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Effects of polystyrene and polylactide nanoparticles on macrophages under a repeated exposure mode
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This study compared the responses of macrophages to repeated low-dose exposure to persistent polystyrene nanoparticles and biodegradable polylactide (PLA) nanoparticles, finding that proteome changes were reduced (PS) or similar (PLA) compared to acute single-dose exposure, indicating cell adaptation. However, PLA particles induced mitochondrial dysfunction and suppressed immune responses to bacterial danger signals, while PS caused slight immune function alterations, indicating harmful effects persisting even under repeated low-dose exposure.
Abstract Micro and nanoplastics are pollutants which concentration in different biotopes increases continuously over time, which poses the question of their potential effects on health. In animals, these micro and nanoplastics are recognized as particulate materials and thus handled by macrophages, which are therefore a key cell type to study. Most studies have used an experimental scheme in which the cells are exposed to a single dose of plastics, with a readout made immediately after exposure. However, this classical experimental scheme does not take into account the impact of biopersistence, nor the potential cellular adaptation that may take place when cells are exposed repeatedly to a low dose of plastics. We thus used a repeated exposure scheme, in order to better take into account these phenomena. Within this frame, we compared the macrophages responses to a persistent nanoplastic, i.e. polystyrene nanoparticles and to a biodegradable nanoplastic, i.e. polylactide, by a combination of proteomic and targeted experiments. Our results show that under this repeated exposure scheme, the proteome changes were of a lesser (for PS) or similar (for PLA) extent than under the acute exposure mode, indicating cell adaptation. However, PLA particles induced mitochondrial dysfunction and depression of response to bacterial molecules perceived as danger signals, such as lipopolysaccharide. Polystyrene nanoparticles also induced a slight alteration of the immune functions of macrophages. This indicates harmful effects even in the repeated exposure scheme.
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Researchers compared how macrophages respond to repeated low-dose exposure to persistent PET nanoparticles versus biodegradable polycaprolactone nanoparticles. They found that cells adapted over repeated exposures, showing less dramatic changes than in single-dose experiments, but PET nanoparticles still induced oxidative stress, reduced phagocytic ability, and triggered pro-inflammatory responses. The study suggests that the biopersistence of conventional plastic nanoparticles like PET may pose more sustained immune system effects compared to biodegradable alternatives.
Effects of true to life polyethylene terephthalate and polycaprolactone nanoparticles on macrophages under a repeated exposure mode
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Researchers exposed macrophages to PET and polycaprolactone nanoparticles under a repeated-dose exposure scheme mimicking chronic environmental exposure, finding that repeated exposures altered immune cell function differently than single-dose protocols commonly used in prior studies.
Effects of micro- and nanoplastic exposure on macrophages: a review of molecular and cellular mechanisms
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This review details how macrophages, key immune cells, respond when they engulf micro- and nanoplastics. The particles trigger inflammatory signaling, damage mitochondria and lysosomes, cause excessive production of harmful reactive oxygen species, and can lead to cell death, while in fat tissue they promote fat buildup and insulin resistance.
A comparison of the effects of polystyrene and polycaprolactone nanoplastics on macrophages
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A comparison of polystyrene and polycaprolactone nanoplastics on macrophage immune cells found both types induced adverse cellular effects, with the study highlighting that plastic persistence in the environment may drive progressive accumulation leading to chronic immune system impacts.
Video S2. Interaction between aged MPs and LP
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After one year in artificial body fluids, polystyrene microplastics showed increased surface roughness and hydrophilicity that enhanced adhesion of lipopolysaccharide, a bacterial toxin. When phagocytosed by macrophages, these aged microplastic-LPS complexes triggered inflammasome activation and pyroptosis, and worsened colitis severity in mice, identifying aged microplastics as 'Trojan horses' for amplifying inflammatory responses.
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