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Variability in bioreactivity linked to changes in size and zeta potential of diesel exhaust particles in human immune cells.

Publication ,  Journal Article
Sarkar, S; Zhang, L; Subramaniam, P; Lee, K-B; Garfunkel, E; Strickland, PAO; Mainelis, G; Lioy, PJ; Tetley, TD; Chung, KF; Zhang, J; Ryan, M ...
Published in: PloS one
January 2014

Acting as fuel combustion catalysts to increase fuel economy, cerium dioxide (ceria, CeO2) nanoparticles have been used in Europe as diesel fuel additives (Envirox™). We attempted to examine the effects of particles emitted from a diesel engine burning either diesel (diesel exhaust particles, DEP) or diesel doped with various concentrations of CeO2 (DEP-Env) on innate immune responses in THP-1 and primary human peripheral blood mononuclear cells (PBMC). Batches of DEP and DEP-Env were obtained on three separate occasions using identical collection and extraction protocols with the aim of determining the reproducibility of particles generated at different times. However, we observed significant differences in size and surface charge (zeta potential) of the DEP and DEP-Env across the three batches. We also observed that exposure of THP-1 cells and PBMC to identical concentrations of DEP and DEP-Env from the three batches resulted in statistically significant differences in bioreactivity as determined by IL-1β, TNF-α, IL-6, IFN-γ, and IL-12p40 mRNA (by qRT-PCR) and protein expression (by ELISPOT assays). Importantly, bioreactivity was noted in very tight ranges of DEP size (60 to 120 nm) and zeta potential (-37 to -41 mV). Thus, these physical properties of DEP and DEP-Env were found to be the primary determinants of the bioreactivity measured in this study. Our findings also point to the potential risk of over- or under- estimation of expected bioreactivity effects (and by inference of public health risks) from bulk DEP use without taking into account potential batch-to-batch variations in physical (and possibly chemical) properties.

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Published In

PloS one

DOI

EISSN

1932-6203

ISSN

1932-6203

Publication Date

January 2014

Volume

9

Issue

5

Start / End Page

e97304

Related Subject Headings

  • Vehicle Emissions
  • Surface Properties
  • Real-Time Polymerase Chain Reaction
  • Particle Size
  • Nanoparticles
  • Middle Aged
  • Male
  • Leukocytes, Mononuclear
  • Immunity, Innate
  • Humans
 

Citation

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Sarkar, S., Zhang, L., Subramaniam, P., Lee, K.-B., Garfunkel, E., Strickland, P. A. O., … Schwander, S. (2014). Variability in bioreactivity linked to changes in size and zeta potential of diesel exhaust particles in human immune cells. PloS One, 9(5), e97304. https://doi.org/10.1371/journal.pone.0097304
Sarkar, Srijata, Lin Zhang, Prasad Subramaniam, Ki-Bum Lee, Eric Garfunkel, Pamela A Ohman Strickland, Gediminas Mainelis, et al. “Variability in bioreactivity linked to changes in size and zeta potential of diesel exhaust particles in human immune cells.PloS One 9, no. 5 (January 2014): e97304. https://doi.org/10.1371/journal.pone.0097304.
Sarkar S, Zhang L, Subramaniam P, Lee K-B, Garfunkel E, Strickland PAO, et al. Variability in bioreactivity linked to changes in size and zeta potential of diesel exhaust particles in human immune cells. PloS one. 2014 Jan;9(5):e97304.
Sarkar, Srijata, et al. “Variability in bioreactivity linked to changes in size and zeta potential of diesel exhaust particles in human immune cells.PloS One, vol. 9, no. 5, Jan. 2014, p. e97304. Epmc, doi:10.1371/journal.pone.0097304.
Sarkar S, Zhang L, Subramaniam P, Lee K-B, Garfunkel E, Strickland PAO, Mainelis G, Lioy PJ, Tetley TD, Chung KF, Zhang J, Ryan M, Porter A, Schwander S. Variability in bioreactivity linked to changes in size and zeta potential of diesel exhaust particles in human immune cells. PloS one. 2014 Jan;9(5):e97304.

Published In

PloS one

DOI

EISSN

1932-6203

ISSN

1932-6203

Publication Date

January 2014

Volume

9

Issue

5

Start / End Page

e97304

Related Subject Headings

  • Vehicle Emissions
  • Surface Properties
  • Real-Time Polymerase Chain Reaction
  • Particle Size
  • Nanoparticles
  • Middle Aged
  • Male
  • Leukocytes, Mononuclear
  • Immunity, Innate
  • Humans