Effects of palladium nanoparticles on the cytokine release from peripheral blood mononuclear cells of non-atopic women

The object of this study is to determine the cytokine release from PBMCs exposed to Pd model nanoparticles emitted from catalytic converters. PBMCs of 8 healthy non-atopic women were incubated in the presence of Pd nanoparticles (5-10 nm) or salt (potassium hexa-chloropalladate) 10-5 and 10-6 M. Rel...

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Veröffentlicht in:Journal of biological regulators and homeostatic agents 2010-04, Vol.24 (2), p.207-214
Hauptverfasser: Boscolo, Paolo, Bellante, V, Leopold, K, Maier, M, Di Giampaolo, L, Antonucci, A, Iavicoli, I, Tobia, L, Paoletti, A, Montalti, M, Petrarca, C, Qiao, N, Sabbioni, E, Di Gioacchino, M
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Sprache:eng
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Zusammenfassung:The object of this study is to determine the cytokine release from PBMCs exposed to Pd model nanoparticles emitted from catalytic converters. PBMCs of 8 healthy non-atopic women were incubated in the presence of Pd nanoparticles (5-10 nm) or salt (potassium hexa-chloropalladate) 10-5 and 10-6 M. Release of cytokines in supernatant of PBMCs was then determined. In cultures without LPS, IL-10 and IL-17 release from PBMCs was inhibited by Pd salt, while Pd nanoparticles inhibited TNF-alpha and IL-17 release. In LPS-stimulated cultures, release of IFN-gamma, TNF-alpha, IL-10 and IL-17 was inhibited by Pd salt, whereas IFN-gamma release was enhanced and TNF-alpha and IL-17 release was inhibited by Pd nanoparticles. In conclusion, Pd salt inhibits cytokine release, whereas Pd nanoparticles exert modulatory effects enhancing the release of IFN-gamma, a Th1 cytokine typical of delayed allergic reactions. This result is interesting considering the increase of allergic contact dermatitis to Pd in people exposed to Pd nanoparticles in urban environments.
ISSN:0393-974X