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May 6, 2026Annals of Work Exposures and Health0 citations

56 Combined microplastic and indoor or urban dust exposure potentiates inflammatory responses in a human alveolar model in vitro

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JBJoshua BatemanEAEric AuyangKMKirsty Meldrum

Key Points

  • The study aims to evaluate the inflammatory responses in an alveolar model due to combined exposure to microplastics and urban dust.
  • In vitro alveolar model with type I and II pneumocytes and macrophages was developed.
  • Aerosol exposure system was used to expose cells to microplastic samples and urban/indoor dust.
  • IL-6 and IL-8 release were measured post-exposure using ELISA.
  • Co-exposure of microplastics with urban dust significantly increased IL-6 levels.
  • Significant IL-8 release observed specifically when polystyrene was co-exposed with either type of dust.
  • No major changes in cell viability or barrier integrity post-exposure.

Abstract

Abstract The potential health effects posed by inhaled micro/nanoplastics (MNPs) is an area of increasing concern. There is therefore a requirement to assess environmentally relevant MNP samples using methods that accurately mirror real human exposures, whilst considering potential concomitant effects of the ambient air pollution mixture. Here, an in vitro alveolar model at the air-liquid interface, comprising anatomically appropriate densities of type I pneumocytes (hAELVi), type II pneumocytes (NCI-H441) and macrophages (differentiated THP-1), was exposed to MNPs using an aerosol exposure system (VITROCELL® Cloud12). Polyamide (PA), polyethylene terephthalate (PET) or polystyrene (PS) were deposited onto cultures by nebulising 200 μL MNP suspension (1 mg/mL) three times, followed by sequential urban dust (SRM 1649b) or indoor dust (SRM 2583) (780 ng/cm2) (NIST) exposure. Twenty-four hours post-exposure, there were no significant changes to cell viability (Erythrosin B assay) or barrier integrity (blue dextran assay). As single pollutants, PET and PS, but not PA non-significantly increased IL-6 and IL-8 release (ELISA). Co-exposure of all MNPs with SRM 1649b or SRM 2583 increased IL-6 and IL-8 release compared to respective single pollutant exposures, however significance was only reached for IL-8 release when PS was co-exposed with either SRM 1649b or SRM 2583 (P 0.05). It is shown here that MNPs may be able to act synergistically with other ambient air pollution samples to induce pulmonary inflammation whereas a single pollutant does not induce this effect, further emphasising the requirements to consider the toxicological profile of realistic air pollutant mixtures on human health.

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Cite This Study

Bateman et al. (2026) studied this question.

synapsesocial.com/papers/69fa8ef304f884e66b5314cahttps://doi.org/10.1093/annweh/wxag024.034
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1125 <i>In vitro</i> toxicity of micro- and nanoplastics in alveolar macrophages and a 3D-alveolar model: influence of size, polymer, and weathering2026
  2. 2Polyamide and polyvinyl chloride microplastics induce cytotoxicity and cytokine release in primary normal human bronchial epithelial cells2026
  3. 3110 <i>In vitro</i> exposure of human lung and macrophage cells to chemical and nanoplastic particle mixtures relevant to indoor environments2026
  4. 4Exploring micro(nano)plastic presence and effects in human airways: in vitro and clinical findings2024
  5. 5Evaluating the toxicity of polystyrene micro- and nanoplastics in human bronchial epithelial cells: differences and challenges using aerosol and suspension exposures2026