4.3 Article

Evaluation of cytokine expression in BEAS cells exposed to fine particulate matter (PM2.5) from specialized indoor environments

Journal

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/09603123.2010.515668

Keywords

air pollutant concentrations; dust; exposure assessment; heavy metals; indoor

Funding

  1. Continuous Research Excellence (MBRS-SCORE)
  2. National Institutes of Heath [5S06-GM008224, 5R25GM061838-08, 2R25GM061838-09]
  3. National Center for Research Resources, National Institutes of Heath [G12RR03051]
  4. Minority Biomedical Research Support - Research Initiative for Scientific Enhancement (MBRS-RISE)
  5. Center for Environmental and Toxicological Research at the University of Puerto Rico Medical Sciences Campus
  6. NATIONAL CENTER FOR RESEARCH RESOURCES [G12RR003051] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R25GM061838, S06GM008224] Funding Source: NIH RePORTER
  8. National Institute on Minority Health and Health Disparities [G12MD007600] Funding Source: NIH RePORTER

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Fine particles were collected in three indoor environments and an outdoor reference site. Samples were acid and aqueous extracted for metal analyses and cytokine expression study using a BEAS-2B line. Results revealed that the average PM2.5 concentration indoors was 5.8 mu g/m(3) while outside, it was 9.4 mu g/m(3). The airborne metal concentrations in indoor air ranged from 0.01 ng/m(3) (Cd) to 620 ng/m(3) (Al). All metals analyzed were higher indoors when compared to outdoor (I/O ratio) indicating a contribution from the workplace. Some metals were more efficiently extracted (e.g., Ni, V, As) in the aqueous phase than others (e.g., Fe and Al). Toxicological assays showed that the aqueous extracts at 20% induced IL-6 and subsequently inhibited it at a higher concentration (50%); both IL-8 and MCP-1 were inhibited at 20 and 50%. As, Ni and V concentrations seem to be the most important metals associated with the cytokine induction/inhibition response probably due to the higher bioavailability.

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