Residual Oil Fly Ash Induces Cytotoxicity and Mucin Secretion by Guinea Pig Tracheal Epithelial Cells via an Oxidant-Mediated Mechanism

• Published in: Toxicology and applied pharmacology 2000-03, Vol.163 (3), p.221-230
• Main Authors: Jiang, Nanfei, Dreher, Kevin L., Dye, Janice A., Li, Yuehua, Richards, Judy H., Martin, Linda D., Adler, Kenneth B.
• Format: Article
• Language: English
• Subjects: Air; Animals; Antioxidants - pharmacology; Biological and medical sciences; Carbon - toxicity; Cell Survival - drug effects; Cells, Cultured; Coal Ash; cytotoxicity; Dust - adverse effects; Environmental pollutants toxicology; Epithelial Cells - drug effects; Gene Expression - drug effects; Guinea Pigs; Industrial Waste; Medical sciences; Metals - toxicity; mucin; mucins; Mucins - biosynthesis; Mucins - genetics; Mucins - secretion; oxidant; Oxidants - pharmacology; Particulate Matter; residual oil fly ash; RNA, Messenger - biosynthesis; RNA, Messenger - genetics; Toxicology; Trachea - cytology; Trachea - drug effects; Trachea - metabolism
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1006/taap.1999.8886

Inhalation of ambient air particulate matter (PM) is associated with pulmonary injury and inflammation. Using primary cultures of guinea pig tracheal epithelial (GPTE) cells as an in vitro model of airway epithelium, we examined effects of exposure to suspensions of six different emission and ambient air PM samples: residual oil fly ash (ROFA) from an electrical power plant; fly ash from a domestic oil burning furnace (DOFA); ambient air dust from St. Louis (STL), Ottawa (OT), and Washington, DC (WDC); and volcanic ash from the eruption of Mount Saint Helens (MSH) in 1980. Effects of these particulates on cell viability (assessed via LDH assay), secretion of mucin (measured by a monoclonal antibody-based ELISA), and steady-state mRNA levels of the mucin gene MUC2 were determined. ROFA was the most toxic of the dusts tested, as it significantly increased LDH release following a 24-h incubation with 50 μg/cm2 ROFA. ROFA also enhanced MUC2 mRNA after 4-h exposure, and mucin secretion after 8 h. ROFA-induced mucin secretion and cytotoxicity were attenuated by the oxidant scavenger, dimethylthiourea (DMTU). ROFA exposure also depleted cells of glutathione (GSH). Relatedly, depletion of intracellular GSH by treatment of the cells with buthionine sulfoxamine (BSO) also provoked mucin secretion, as well as enhancing the secretory effect of ROFA when the two agents were added together. L-NMA, the nitric oxide synthase (NOS) inhibitor, did not affect ROFA-induced mucin secretion. Of the soluble transition metals in ROFA (nickel, iron, vanadium), only vanadium individually, or combinations of the metals containing vanadium, provoked secretion. The results suggest ROFA enhances mucin secretion and generates toxicity in vitro to airway epithelium via a mechanism(s) involving generation of oxidant stress, perhaps related to depletion of cellular antioxidant capacity. Deleterious effects of inhalation of ROFA in the respiratory tract in vivo may relate to these cellular responses. Vanadium, a component of ROFA, may be important in generating these reactions.