Toxicological Responses of α-Pinene-Derived Secondary Organic Aerosol and Its Molecular Tracers in Human Lung Cell Lines

dc.bibliographicCitation.firstPage817eng
dc.bibliographicCitation.issue3eng
dc.bibliographicCitation.journalTitleChemical research in toxicologyeng
dc.bibliographicCitation.lastPage832eng
dc.bibliographicCitation.volume34eng
dc.contributor.authorKhan, Faria
dc.contributor.authorKwapiszewska, Karina
dc.contributor.authorZhang, Yue
dc.contributor.authorChen, Yuzhi
dc.contributor.authorLambe, Andrew T.
dc.contributor.authorKołodziejczyk, Agata
dc.contributor.authorJalal, Nasir
dc.contributor.authorRudzinski, Krzysztof
dc.contributor.authorMartínez-Romero, Alicia
dc.contributor.authorFry, Rebecca C.
dc.contributor.authorSurratt, Jason D.
dc.contributor.authorSzmigielski, Rafal
dc.date.accessioned2022-03-29T12:40:02Z
dc.date.available2022-03-29T12:40:02Z
dc.date.issued2021
dc.description.abstractSecondary organic aerosol (SOA) is a major component of airborne fine particulate matter (PM2.5) that contributes to adverse human health effects upon inhalation. Atmospheric ozonolysis of α-pinene, an abundantly emitted monoterpene from terrestrial vegetation, leads to significant global SOA formation; however, its impact on pulmonary pathophysiology remains uncertain. In this study, we quantified an increasing concentration response of three well-established α-pinene SOA tracers (pinic, pinonic, and 3-methyl-1,2,3-butanetricarboxylic acids) and a full mixture of α-pinene SOA in A549 (alveolar epithelial carcinoma) and BEAS-2B (bronchial epithelial normal) lung cell lines. The three aforementioned tracers contributed ∼57% of the α-pinene SOA mass under our experimental conditions. Cellular proliferation, cell viability, and oxidative stress were assessed as toxicological end points. The three α-pinene SOA molecular tracers had insignificant responses in both cell types when compared with the α-pinene SOA (up to 200 μg mL-1). BEAS-2B cells exposed to 200 μg mL-1 of α-pinene SOA decreased cellular proliferation to ∼70% and 44% at 24- and 48-h post exposure, respectively; no changes in A549 cells were observed. The inhibitory concentration-50 (IC50) in BEAS-2B cells was found to be 912 and 230 μg mL-1 at 24 and 48 h, respectively. An approximate 4-fold increase in cellular oxidative stress was observed in BEAS-2B cells when compared with untreated cells, suggesting that reactive oxygen species (ROS) buildup resulted in the downstream cytotoxicity following 24 h of exposure to α-pinene SOA. Organic hydroperoxides that were identified in the α-pinene SOA samples likely contributed to the ROS and cytotoxicity. This study identifies the potential components of α-pinene SOA that likely modulate the oxidative stress response within lung cells and highlights the need to carry out chronic exposure studies on α-pinene SOA to elucidate its long-term inhalation exposure effects. © 2021 American Chemical Society.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/8447
dc.identifier.urihttps://doi.org/10.34657/7485
dc.language.isoengeng
dc.publisherNew York, NY : ACS Publ.eng
dc.relation.doihttps://doi.org/10.1021/acs.chemrestox.0c00409
dc.relation.essn1520-5010
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc610eng
dc.subject.other3 methyl 1,2,3 butanetricarboxylic acideng
dc.subject.otherhydroperoxideeng
dc.subject.otherpineneeng
dc.subject.otherpinic acideng
dc.subject.otherpinonic acideng
dc.subject.otherreactive oxygen metaboliteeng
dc.subject.othertracereng
dc.subject.otherunclassified drugeng
dc.subject.otherA-549 cell lineeng
dc.subject.otherBEAS-2B cell lineeng
dc.subject.othercell proliferationeng
dc.subject.othercell viabilityeng
dc.subject.otherconcentration responseeng
dc.subject.othercytotoxicityeng
dc.subject.otherHL cell lineeng
dc.subject.otherIC50eng
dc.subject.otheroxidative stresseng
dc.subject.othersecondary organic aerosoleng
dc.subject.othertoxicologyeng
dc.titleToxicological Responses of α-Pinene-Derived Secondary Organic Aerosol and Its Molecular Tracers in Human Lung Cell Lineseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorTROPOSeng
wgl.subjectMedizin, Gesundheiteng
wgl.typeZeitschriftenartikeleng
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