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. 2024 Aug 22;25:321. doi: 10.1186/s12931-024-02951-7

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

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Fig. 1 — PM induced intracellular ROS formation in BEAS-2B cells. Intracellular ROS formation was detected using DCF-DA dye. The concentration (A) and time (B) dependent increases in the levels of intracellular ROS were observed. (C) ROS scavenger, NAC, significantly inhibited PM-induced ROS production in BEAS-2B cells. (D) In addition, the WST-1 assay was employed to assess metabolic activity of cells following exposure to PM. ^***P < 0.001 and ^**P < 0.01, compared with untreated cells (control); ^##P < 0.01 and ^#P < 0.05, compared with the PM-stimulated group (n = 3)