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Abstract Background Ambient particulate matter (PM) exposure is associated with respiratory and cardiovascular morbidity and mortality. To what extent such effects are different for PM obtained from different sources or locations is still unclear. This study investigated the in vitro toxicity of ambient PM collected at different sites in the Netherlands in relation to PM composition and oxidative potential. Method PM was sampled at eight sites: three traffic sites, an underground train station, as well as a harbor, farm, steelworks, and urban background location. Coarse (2.5-10 μm), fine (< 2.5 μm) and quasi ultrafine PM (qUF; < 0.18 μm) were sampled at each site. Murine macrophages (RAW 264.7 cells) were exposed to increasing concentrations of PM from these sites (6.25-12.5-25-50-100 μg/ml; corresponding to 3.68-58.8 μg/cm2). Following overnight incubation, MTT-reduction activity (a measure of metabolic activity) and the release of pro-inflammatory markers (Tumor Necrosis Factor-alpha, TNF-α; Interleukin-6, IL-6; Macrophage Inflammatory Protein-2, MIP-2) were measured. The oxidative potential and the endotoxin content of each PM sample were determined in a DTT- and LAL-assay respectively. Multiple linear regression was used to assess the relationship between the cellular responses and PM characteristics: concentration, site, size fraction, oxidative potential and endotoxin content. Results Most PM samples induced a concentration-dependent decrease in MTT-reduction activity and an increase in pro-inflammatory markers with the exception of the urban background and stop & go traffic samples. Fine and qUF samples of traffic locations, characterized by a high concentration of elemental and organic carbon, induced the highest pro-inflammatory activity. The pro-inflammatory response to coarse samples was associated with the endotoxin level, which was found to increase dramatically during a three-day sample concentration procedure in the laboratory. The underground samples, characterized by a high content of transition metals, showed the largest decrease in MTT-reduction activity. PM size fraction was not related to MTT-reduction activity, whereas there was a statistically significant difference in pro-inflammatory activity between Fine and qUF PM. Furthermore, there was a statistically significant negative association between PM oxidative potential and MTT-reduction activity. Conclusion The response of RAW264.7 cells to ambient PM was markedly different using samples collected at various sites in the Netherlands that differed in their local PM emission sources. Our results are in support of other investigations showing that the chemical composition as well as oxidative potential are determinants of PM induced toxicity in vitro.

http://dx.doi.org/10.1289/ehp.1205860R We thank Gangamma for a number of excellent observations and would like to respond to the issues raised. Gangamma points out that the levels of fractional exhaled nitric oxide [...]

A letter to the editor is presented in response to the article "Airborne Particulate Matter and Acute Lung Inflammation," that was published in a previous issue.

Abstract: Accurate measurements of SO2 at low ambient concentrations are needed in order to investigate the role of SO2 in particle nucleation events and the long-term impact of reductions in sulfur emissions in recent decades. In this study, artifacts in SO2 concentration measurements were investigated using two identical ion chromatography-based instruments (the Gas Particle Ion Chromatograph, GP-IC, Dionex Corporation) and two identical UV fluorescence-based SO2 analyzers (the TECO 43CTL, an industry standard). The SO2 concentration values measured with the GP-IC at roadside sites were compared with simultaneous side-by-side measurements made with the fluorescence analyzers. The SO2 concentration measured with the GP-IC had an ∼30% negative calibration artifact. When the GP-ICs were calibrated using an improved procedure developed in the course of this study, only a ±5% difference from the TECO analyzers remained, except under high NO concentration conditions. The fluorescence analyzers exhibited a positive artifact under elevated NO concentration conditions. Sulfur oxidation ratios were calculated based on the GP-IC-measured SO2 and SO4 2- concentrations and used to help identify potential emission sources. The SO2 concentrations measured with the GP-IC were also compared to data obtained from a National Air Pollution Surveillance (NAPS) speciation sampler equipped with a Na2CO3-coated denuder. Good correlation between SO2 data from the two methods was seen during five months of measurement, but the GP-IC SO2 data were ∼30% lower than the NAPS data. Deposition of SO2 within an urban street canyon is discussed as a possible explanation for this difference. [Copyright &y& Elsevier]