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Chemical Clustering Analysis of Ambient and Emission Source Particulate Matter Reveals Compositional Determinants of Pulmonary Toxicity Responses

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Comparative toxicological studies of heterogeneous particulate matter (PM) samples are needed to evaluate the influence of particle chemistry on pulmonary toxicity outcomes. Here, groups of mice were exposed by oropharyngeal aspiration of a 100 μg dose of one of seven PM samples, including three coarse and two fine ambient air PM, and 2 fine emission source PM. Acute inflammatory and lung injury markers in the bronchoalveolar lavage fluid (BALF) were assessed. A weighted chemical correlation network analysis (WCCNA) clustered PM chemical constituents into four modules based on comodulation within samples. These modules and their components were then correlated with lung toxicity end points. One module represented the highest levels of zinc, lead, copper, and tin, and was strongly correlated with BALF neutrophils, macrophage inflammatory protein-2, and several markers of lung injury. A second module represented the highest levels of several toxic transition metals including magnesium, nickel, vanadium, and cobalt, and was strongly correlated with pro-inflammatory interleukin-6, in addition to neutrophils, albumin, and lactate dehydrogenase. A third module, represented by high levels of elemental carbon, nitrate, sulfate, and phosphate, was correlated with pro-inflammatory tumor necrosis factor-α (TNF-α), in addition to BALF protein and other lung injury markers. The final module consisted of 7 elements associated with the 3 coarse crustal PM samples, and these individual elements exhibited moderate correlations with BALF neutrophils and TNF-α. Toxic transition metals produced the greatest effects on lung toxicity, followed by anions and carbon species. These studies demonstrated that chemical and toxicological assessments of heterogeneous samples of PM produce clusters of chemical constituents that can be correlated with separate toxicological outcomes.

Impact/Purpose

Understanding which chemical components of particulate matter (PM) samples have the potential to drive toxicity remains a challenge because of the diverse physicochemical constituents of PM. In this study, seven ambient PM samples were tested, including coarse PM from Cleveland Ohio (CLC), Ottawa Ontario (OTC), and Dearborn Michigan (DBC), fine PM from Detroit Michigan (summer, DSF and winter, DWF), and emission source fine PM samples of residual oil fly ash (ROF) and diesel exhaust (DEF). We used a weighted chemical correlation network analysis (WCCNA) to better understand inter-chemical relationships and relationships between chemicals and lung toxicity outcomes, which produced 4 coded modules based on their relative abundance across PM samples. The brown module, consisting of elements dominant in the coarse Ottawa PM sample (OTC), was correlated with the broadest spectrum of toxicity endpoints, but especially BALF neutrophils and MIP-2. Toxic transition metals including Mg, Ni, V, and Co were strongly represented in the turquoise module and dominant in the fine residual oil fly ash (ROF) PM sample, which had a more selective impact on toxicity endpoints, including neutrophils and IL-6. The gray module included elemental carbon and all measured anions, and correlated with TNF-a, BALF protein and other lung injury markers. Elements associated with coarse crustal PM samples CLC, OTC, and DBC comprised the final blue module, which was associated with moderate levels of neutrophils and TNF-a. Recent studies provide strong evidence that the chemistry of PM plays a significant role in toxicological impacts. Accordingly, our approach of correlating chemical constituents of PM with lung toxicity endpoints can help to inform risk characterization of inhaled PM.

Citation

Klein, L., S. Gavett, Joseph Pancras, W. Williams, A. Nored, Ian Gilmour, AND Yong Ho Kim. Chemical Clustering Analysis of Ambient and Emission Source Particulate Matter Reveals Compositional Determinants of Pulmonary Toxicity Responses. American Chemical Society, Washington, DC, 39(3):319-328, (2026). [DOI: 10.1021/acs.chemrestox.5c00390]

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DOI: Chemical Clustering Analysis of Ambient and Emission Source Particulate Matter Reveals Compositional Determinants of Pulmonary Toxicity Responses
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Last updated on June 24, 2026
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