Toxicity and inflammatory potential of mineral fibres: The contribute of released soluble metals versus cell contact direct effects.

Asbestos fibres have been considered an environmental hazard for decades. However, little is known about the attempts of circulating immune cells to counteract their toxicity. We addressed the early effects of fibre‐released soluble factors (i.e. heavy metals) in naïve immune cells, circulating immediately below the alveolar/endothelial cell layer. By comparison, the direct fibre effects on endotheliocytes were also studied since these cells are known to sustain inflammatory processes. The three mineral fibres analysed showed that mainly chrysotile (CHR) and erionite (ERI) were able to release toxic metals in extracellular media respect to crocidolite (CRO), during the first 24 h. Nevertheless, all three fibres were able to induce oxidative stress and genotoxic damage in indirectly challenged naïve THP‐1 monocytes (separated by a membrane). Conversely, only CHR‐released metal ions induced apoptosis, NF‐κB activation, cytokines and CD163 gene overexpression, indicating a differentiation towards the M0 macrophage phenotype. On the other hand, all three mineral fibres in direct contact with HECV endothelial cells showed cytotoxic, genotoxic and apoptotic effects, cytokines and ICAM‐I overexpression, indicating the ability of these cells to promote an inflammatory environment in the lung independently from the type of inhaled fibre. Our study highlights the different cellular responses to mineral fibres resulting from both the nature of the cells and their function, but also from the chemical–physical characteristics of the fibres. In conclusion, CHR represented the main pro‐inflammatory trigger, able to recruit and activate circulating naïve monocytes, through its released metals, already in the first 24 h after inhalation. The early effects of mineral fibre‐released heavy metals in THP‐1 cells, mimicking the immune cells in the alveolar capillaries, were investigated, and by comparison, also the direct fibre effects on the endothelial cell layer. The study highlights that the cellular responses result from the nature of the cells, their function and from the fibre chemical–physical characteristics. CHR represented the main pro‐inflammatory trigger, able to recruit and activate circulating monocytes, through its released metals, already at 24 h after inhalation. [ABSTRACT FROM AUTHOR]