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Polyamide and polyvinyl chloride microplastics induce cytotoxicity and cytokine release in primary normal human bronchial epithelial cells
Summary
Scientists exposed lung cells from human airways to tiny plastic particles (from nylon and PVC, two common plastics) to see how they'd react, similar to what might happen when we breathe in airborne microplastics. The smallest particles caused cell damage and triggered inflammation-related signals, with PVC causing harm at lower doses than nylon—suggesting the type and size of plastic particles we inhale may matter for lung health. This is early-stage lab research, so more studies are needed to confirm what this means for people breathing in real-world air.
Abstract Our daily and continuous exposure to airborne micro- and nanoplastics (MNPs) together with the limited information on their potential hazards, warrants the need for more information on MNP-toxicity. In this study, we investigated the effects of diverse size ranges of amorphous MNPs from environmentally relevant polymers, on Air-Liquid-Interface (ALI)-cultured Normal Human Bronchial Epithelial cells (NHBEs) by analyzing immunological response parameters 24 h after exposure. In addition, we have used this setup to compare the responses of NHBEs to MNPs using nebulization or quasi-ALI (small droplet) exposure. NHBEs responded differently to exposures of polyamide (PA) or polyvinyl chloride (PVC) particles at nominal doses between 0.003 and 0.100 µg/cm 2 . PA particles < 1 μm (but not those > 1 μm) induced dose-dependent cell death, increased IL-8 secretion and decreased MCP-1 secretion. PVC particles (< 1 μm and 1–5 μm) induced cell death at lower concentrations than PA particles. Also, an increased IL-8 secretion and decreased MCP-1 secretion was observed for PVC particles in all size fractions (< 1 μm, 1–5 μm and 5–10 μm). Comparison of nebulization versus quasi-ALI exposure indicated differences related to the exposure method, but further experimental assessment is needed for definite conclusions and to ensure that the obtained data is relevant for toxicological effects occurring in humans. Our results indicate that PA and PVC particles increase IL-8 secretion and, PA only, decreases MCP-1 secretion. It needs to be established whether these effects on cytokines also indicate an activation of immune cells.