The identification of the major contributors in atmospheric particulate matter to oxidative stress using surrogate particles

2021 
Oxidative stress is a unifying mechanism relating to the adverse effects induced by atmospheric particulate matter (PM). Owing to complex compositions, the role of PM constituents in triggering oxidative stress remains unclear. We employed synthetic particle suspensions with controlled sizes and compositions as PM surrogates to identify the key contributors to oxidative stress. The suspensions consisted of carbon black (CB) particles, polycyclic aromatic hydrocarbon adsorbed on CB, and dissolved metal ions. After the exposure of A549 or BEAS-2B cells to CB particles, the reactive oxygen species (ROS) level increased in a manner that was dependent on the size and concentration of the particles, in the order of 14 nm > 56 nm > 260 nm. Benzo[a]pyrene-coated CB also increased the ROS level, but not as much as the naked CB, and the benzo[a]pyrene-dione coating had no effect. The co-exposure of CB with one of the eight metal ions did not lead to any additional ROS increase. The results indicate that among the three major constituents, CB particles, and the small-sized ones in particular, contributed most to ROS generation. In mechanistic studies, damaged mitochondria cristae were observed, suggesting that mitochondria are one of the target organelles. Both naked and BaP-coated CB decreased the mitochondrial membrane potential and changed the mRNA expression of fusion/fission proteins. ROS inhibition experiments suggest that complex I of the mitochondria was involved, but complex III and the NADPH oxidase (NOX) system were not. It was thus postulated that small-sized particles could enter cells and disrupt the mitochondria, particularly complex I, leading to the elevated generation of ROS. Our work calls for more attention to be paid to the toxicity of the ultrafine fractions of PM.
    • Correction
    • Source
    • Cite
    • Save
    • Machine Reading By IdeaReader
    68
    References
    0
    Citations
    NaN
    KQI
    []