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Toxicity of real-world PM<sub>2.5</sub> road tunnel emissions using a mobile air-liquid interface system and submerged exposure

Introna, Micol; Juárez-Facio, Ana Teresa; Srikanth Vallabani, Naga Veera; Tu, Ming Hui; Heikkilä, Paavo; Colombo, Andrea; Liboni, Valentina; Tsyupa, Bozhena; Mancini, Alessandro; Keskinen, Jorma; Olofsson, Ulf; Steimer, Sarah Sulamith; Karlsson, Hanna Lovisa; Elihn, Karine (2025-08-15)

 
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Introna, Micol
Juárez-Facio, Ana Teresa
Srikanth Vallabani, Naga Veera
Tu, Ming Hui
Heikkilä, Paavo
Colombo, Andrea
Liboni, Valentina
Tsyupa, Bozhena
Mancini, Alessandro
Keskinen, Jorma
Olofsson, Ulf
Steimer, Sarah Sulamith
Karlsson, Hanna Lovisa
Elihn, Karine
15.08.2025

Environmental Pollution
126486
doi:10.1016/j.envpol.2025.126486
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202507297879

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Peer reviewed
Tiivistelmä
Traffic-related air pollution is a major public health concern, contributing to respiratory and cardiovascular diseases worldwide. The aim of this study was to investigate the feasibility of using a mobile Air-Liquid Interface (ALI) system to assess the cytotoxicity and inflammatory potential of freshly generated PM2.5 (particle matter with aerodynamic diameter <2.5 μm) in a road tunnel in Stockholm. We hypothesized that cellular effects would be detectable at lower doses compared to submerged exposures. The mean particle dose in ALI was 1.4 ± 0.8 μg/cm2, whereas a wide range of doses was used for submerged exposures. ALI and submerged results showed that PM2.5 from the road tunnel did not affect the viability of A549 cells, whereas a significant and dose-dependent decrease in viability of dTHP-1 (in submerged exposure) was observed. Furthermore, in A549 in ALI a slight increase in inflammatory response (IL-8, IL-6, and IL-1β) was observed. In submerged exposure, the inflammatory response was clearer, particularly in the dTHP-1 cells. In conclusion, this study presents the first successfully conducted in situ ALI exposure in a road tunnel. The results demonstrate that dTHP-1 cells exhibit clear cytotoxic and inflammatory responses, while A549 show only weak effects. These findings suggest that co-cultures of A549 and dTHP-1 may be valuable in future ALI studies.
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