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Title: In vitro inflammatory and cytotoxic effects of size-segregated particulate samples collected during long-range transport of wildfire smoke to Helsinki

Journal Article · · Toxicology and Applied Pharmacology
 [1];  [1];  [1];  [1];  [1];  [2];  [3];  [2];  [1]
  1. National Public Health Institute, Department of Environmental Health, PO Box 95, FI-70701 Kuopio (Finland)
  2. Finnish Meteorological Institute, Air Quality Research, Helsinki (Finland)
  3. Technical Research Centre of Finland, VTT Processes, Espoo (Finland)

The impact of long-range transport (LRT) episodes of wildfire smoke on the inflammogenic and cytotoxic activity of urban air particles was investigated in the mouse RAW 264.7 macrophages. The particles were sampled in four size ranges using a modified Harvard high-volume cascade impactor, and the samples were chemically characterized for identification of different emission sources. The particulate mass concentration in the accumulation size range (PM{sub 1-0.2}) was highly increased during two LRT episodes, but the contents of total and genotoxic polycyclic aromatic hydrocarbons (PAH) in collected particulate samples were only 10-25% of those in the seasonal average sample. The ability of coarse (PM{sub 10-2.5}), intermodal size range (PM{sub 2.5-1}), PM{sub 1-0.2} and ultrafine (PM{sub 0.2}) particles to cause cytokine production (TNF{alpha}, IL-6, MIP-2) reduced along with smaller particle size, but the size range had a much smaller impact on induced nitric oxide (NO) production and cytotoxicity or apoptosis. The aerosol particles collected during LRT episodes had a substantially lower activity in cytokine production than the corresponding particles of the seasonal average period, which is suggested to be due to chemical transformation of the organic fraction during aging. However, the episode events were associated with enhanced inflammogenic and cytotoxic activities per inhaled cubic meter of air due to the greatly increased particulate mass concentration in the accumulation size range, which may have public health implications.

OSTI ID:
20850420
Journal Information:
Toxicology and Applied Pharmacology, Vol. 215, Issue 3; Other Information: DOI: 10.1016/j.taap.2006.03.007; PII: S0041-008X(06)00106-2; Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0041-008X
Country of Publication:
United States
Language:
English