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Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Human Health Effects Nanoplastics Sign in to save

Sterile inflammation induced by respirable micro and nano polystyrene particles in the pathogenesis of pulmonary diseases

Toxicology Research 2024 11 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 60 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Giuseppa Visalli, Alessio Facciolà, A. Laganà, Giuseppa Visalli, A. Laganà, A. Laganà, A. Laganà, A. Laganà, Alessio Facciolà, Giuseppa Visalli, A. Laganà, Giuseppa Visalli, Consuelo Celesti, Giuseppa Visalli, Giuseppa Visalli, Alessio Facciolà, Alessio Facciolà, Alessio Facciolà, Alessio Facciolà, Giuseppa Visalli, Caterina Saija, Daniela Iannazzo, Consuelo Celesti, Consuelo Celesti, Angela Di Pietro Maria Paola Bertuccio, Alessio Facciolà, Alessio Facciolà, Caterina Saija, Maria Paola Bertuccio, Alessio Facciolà, Daniela Iannazzo, Daniela Iannazzo, Giuseppa Visalli, Angela Di Pietro Angela Di Pietro Angela Di Pietro A. Laganà, Barbara Baluce, Barbara Baluce, Consuelo Celesti, Consuelo Celesti, Angela Di Pietro Daniela Iannazzo, Angela Di Pietro Daniela Iannazzo, Angela Di Pietro

Summary

Researchers exposed human lung and immune cells to polystyrene micro and nanoparticles and found they triggered a type of inflammation that does not require infection, called sterile inflammation. Aged (oxidized) particles and those that interacted with immune cells were especially potent at activating inflammatory pathways including the NLRP3 inflammasome. This suggests that breathing in airborne microplastics could cause chronic lung inflammation over time.

Polymers

Sterile inflammation is involved in the lung pathogenesis induced by respirable particles, including micro- and nanoplastics. Their increasing amounts in the ambient and in indoor air pose a risk to human health. In two human cell lines (A549 and THP-1) we assessed the proinflammatory behavior of polystyrene nanoplastics (nPS) and microplastics (mPS) (Ø 0.1 and 1 μm). Reproducing environmental aging, in addition to virgin, the cells were exposed to oxidized nPS/mPS. To study the response of the monocytes to the inflammatory signal transmitted by the A549 through the release of soluble factors (e.g. alarmins and cytokines), THP-1 cells were also exposed to the supernatants of previously nPS/mPS-treated A549. After dynamic-light-scattering (DLS) analysis and protein measurements for the assessment of protein corona in nPS/mPS, real-time PCR and enzyme-linked-immunosorbent (ELISA) assays were performed in exposed cells. The pro-inflammatory effects of v- and ox-nPS/mPS were attested by the imbalance of the Bax/Bcl-2 ratio in A549, which was able to trigger the inflammatory cascade, inhibiting the immunologically silent apoptosis. The involvement of NFkB was confirmed by the overexpression of p65 after exposure to ox-nPS and v- and ox-mPS. The fast and higher levels of IL-1β, only in THP-1 cells, underlined the NLPR3 inflammasome activation.

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