NPs | cell response | cell frequence/activity | Potential effect |
---|---|---|---|
TiO2 (6-48 h) | |||
↗ expression of TLR (TLR3, TLR4, TLR7 and TLR10) [126, 128] | ↗ naïve T cells [122] | ||
↗ pro-inflammatory cytokines (IL-6, TNF-α, IL1-β) [121,122,123, 127, 130,131,132] | |||
↗ chemokines secretion (IL-8 and CXCL1) ↙ activity (IL-8) [122, 133] | ↗ mast cell activation [134] | ||
↗ co-stimulatory molecules (CD80 and CD86) [122, 123, 131, 132] | ↙ neutrophil and μɸ mobility [133] | ||
NETosis: inflammation, necrosis and apoptosis [124] | |||
↗ β-hexosaminidase release [134] | |||
inflammasome activation [123] | |||
SiO2 (6-48 h) | |||
↗ pro inflammatory cytokines (IL1-β, IL-2, TNF-α) [121, 123, 126, 138, 139, 141] | |||
↙ TLR9 expression [126] | ↗ neutrophil activity [142] | ↗ Susceptibility IBD [123, 126, 140], autoimmune diseases [139, 140] | |
↗ oxidative stress (ROS) [125] | ↗ cross-presentation [141] | NETosis: inflammation, necrosis and apoptosis [142] | |
inflammasome activation [123] | |||
NFkB activation [138] | Susceptibility to infection [126] | ||
↗ DNA release – NET [142] | Allergic response [135] | ||
ZnO (6-48 h) | ↗ pro inflammatory cytokines (IL-1β, TNF-α, IL-6, IFN-ɣ) [125, 130, 143, 144] | Cytotoxicity and inflammation [125, 129, 130, 134, 143, 146] | |
↙ Lymphocytes [146] | |||
↗ neutrophil functions [136] | Chronic pathologies [143] | ||
induces neo-synthesis of polypeptides [144] | ↙ mast cell activation [134] | ||
↗ eosinophils [144] | |||
Genomic instability [146] | |||
↙ β-hexosaminidase and histamine release [134] | Cell cycle imbalanced [125] | ||
Ag (6-48 h) | |||
↗ DNA damage [148] | |||
inflammasome activation [147] | |||