Seasonal Variation in PM2.5 Composition Modulates Oxidative Stress and Neutrophilic Inflammation with Involvement of TLR4 Signaling

Seasonal fluctuations in the chemical composition of fine particulate matter (PM<sub>2.5</sub>) are known to influence its toxicological properties; however, their integrated biological effects remain incompletely understood. In this study, PM<sub>2.5</sub> was continuously collected over two consecutive years at a single urban site in Japan and classified by season. The samples were comprehensively characterized for ionic species, metals, carbonaceous fractions, and polycyclic aromatic hydrocarbons (PAHs), and their pulmonary effects were evaluated in vivo following intratracheal administration in mice. Seasonal PM<sub>2.5</sub> exhibited pronounced compositional differences, with higher levels of secondary inorganic aerosol components in summer and enrichment of PAHs and mineral-associated components in winter. These seasonal differences translated into distinct biological responses. Reactive oxygen species (ROS) production (1.6-2.7-fold increase) and bronchoalveolar lavage (BAL) neutrophil infiltration were strongly associated with PAH-rich PM<sub>2.5</sub>, whereas interleukin-1α (IL-1α) showed robust positive correlations with mineral components, including K<sup>+</sup>, Ca<sup>2+</sup>, and Mg<sup>2+</sup>, which were predominantly enriched in winter PM<sub>2.5</sub>. In contrast, secondary inorganic aerosol species displayed a limited capacity to induce IL-1α. Compared with summer samples, winter PM<sub>2.5</sub> induced significantly higher levels of ROS production and IL-1α (approximately 1.5-2.6-fold increase). Using TLR2- and TLR4-deficient mice, we further demonstrated that PM<sub>2.5</sub>-induced increases in BAL cell counts, ROS, IL-6, and TNF-α were partially attenuated in TLR4 knockout mice, indicating a contributory but not exclusive role for TLR4 signaling in PM<sub>2.5</sub>-driven pulmonary inflammation. Collectively, these findings demonstrate that seasonal variations in PM<sub>2.5</sub> composition, not particle mass alone, critically shape oxidative stress and innate immune responses in the lungs. In particular, winter PM<sub>2.5</sub> enriched in mineral-associated components preferentially activates IL-1α-mediated alarmin pathways, underscoring the importance of the particle composition in determining seasonal air pollution toxicity.

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Journal
Antioxidants
Published
2026-01-09
DOI
https://doi.org/10.3390/antiox15010089
Primary Topic
Air Quality and Health Impacts
Type
article
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article

Seasonal Variation in PM2.5 Composition Modulates Oxidative Stress and Neutrophilic Inflammation with Involvement of TLR4 Signaling

R. OKAZAKI, Tomoaki Okuda, Duo Wang, Zirui Zeng et al.
Antioxidants
Air Quality and Health Impacts
article

Seasonal Variation in PM2.5 Composition Modulates Oxidative Stress and Neutrophilic Inflammation with Involvement of TLR4 Signaling

R. OKAZAKI, Tomoaki Okuda, Duo Wang, Zirui Zeng, Yasuhiro Yoshida, Ryoko Baba, Aya Nawata
article en

Abstract

Seasonal fluctuations in the chemical composition of fine particulate matter (PM<sub>2.5</sub>) are known to influence its toxicological properties; however, their integrated biological effects remain incompletely understood. In this study, PM<sub>2.5</sub> was continuously collected over two consecutive years at a single urban site in Japan and classified by season. The samples were comprehensively characterized for ionic species, metals, carbonaceous fractions, and polycyclic aromatic hydrocarbons (PAHs), and their pulmonary effects were evaluated in vivo following intratracheal administration in mice. Seasonal PM<sub>2.5</sub> exhibited pronounced compositional differences, with higher levels of secondary inorganic aerosol components in summer and enrichment of PAHs and mineral-associated components in winter. These seasonal differences translated into distinct biological responses. Reactive oxygen species (ROS) production (1.6-2.7-fold increase) and bronchoalveolar lavage (BAL) neutrophil infiltration were strongly associated with PAH-rich PM<sub>2.5</sub>, whereas interleukin-1α (IL-1α) showed robust positive correlations with mineral components, including K<sup>+</sup>, Ca<sup>2+</sup>, and Mg<sup>2+</sup>, which were predominantly enriched in winter PM<sub>2.5</sub>. In contrast, secondary inorganic aerosol species displayed a limited capacity to induce IL-1α. Compared with summer samples, winter PM<sub>2.5</sub> induced significantly higher levels of ROS production and IL-1α (approximately 1.5-2.6-fold increase). Using TLR2- and TLR4-deficient mice, we further demonstrated that PM<sub>2.5</sub>-induced increases in BAL cell counts, ROS, IL-6, and TNF-α were partially attenuated in TLR4 knockout mice, indicating a contributory but not exclusive role for TLR4 signaling in PM<sub>2.5</sub>-driven pulmonary inflammation. Collectively, these findings demonstrate that seasonal variations in PM<sub>2.5</sub> composition, not particle mass alone, critically shape oxidative stress and innate immune responses in the lungs. In particular, winter PM<sub>2.5</sub> enriched in mineral-associated components preferentially activates IL-1α-mediated alarmin pathways, underscoring the importance of the particle composition in determining seasonal air pollution toxicity.

AntioxidantsVol. 15(1)
University of Occupational and Environmental Health Japan (JP), Keio University (JP)
Sustainable cities and communities
Openalex Percentile: Top 93%
Air Quality and Health Impacts
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