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METALS MIMIC AIRWAY EPITHELIAL INJURY INDUCED BY IN VITRO EXPOSURE TO UTAH VALLEY AMBIENT PARTICULATE MATTER EXTRACTS
Citation:
Pagan, I, D L. Costa, J K. McGee, J H. Richards, AND J A. Dye. METALS MIMIC AIRWAY EPITHELIAL INJURY INDUCED BY IN VITRO EXPOSURE TO UTAH VALLEY AMBIENT PARTICULATE MATTER EXTRACTS. JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH 66(Part A):1087-1112, (2003).
Description:
Abstract
Epidemiologic studies have shown positive associationsbetween changes in ambient particulate matter (PM) levels in Utah Valley during 1986-1988, and the respiratory health of the local population. Ambient PM reductions coincided withclosure of an open-hearth steel mill, the major industrial source of particulate emissions in the Valley. In this report, water-extracts of PM filters from steel mill operational (UE-86, UE-88) and closure (UE-87) periods were analyzed for their elemental composition. Their relative toxicity was determined by exposing primary rodent airway epithelial cultures to equal masses of extracted material To elucidate extract subcomponents mediating the effects observed, cells were also exposed to surrogate metal mixtures. Potential interactions between the two predominant metals in the UE-86/88 samples, zinc (Zn) and copper (Cu), were further investigated. Data indicated that, relative to the UE-87 (plant closed) sample, UE-86/88 samples contained more sulfate, calcium, potassium, magnesium, and although present in much lower amounts, a variety of metals including: Zn, Cu, iron, lead, strontium, nickel, manganese, and vanadium (V). Cell exposure to UE-86 and UE-88, but not UE-87, resulted in time- and concentration-dependent epithelial injury based on biochemical and light/electron microscopic changes. Cell injury induced by metal mixtures containing equivalent amounts of Zn+Cu+V was commensurate with that induced by the corresponding extract, although divergent antioxidant responses were observed. Exposure to Zn+Cu resulted in significantly greater epithelial toxicity and stress (c-Jun N-terminal protein kinase activation) responses than did exposure to Zn or Cu individually. The parallel epithelial injury induced by the extracts and their surrogate Zn+Cu+V mixtures suggests that these metals are mediating the acute airway epithelial effects observed, however, metal interactions appear to play a critical role in the overall cellular effects induced by the PM-derived extracts. These experimental findings are in good accord with epidemiologic reports of adverse airway and respiratory health effects in Utah Valley residents.