Antagonistic Cytoprotective Effects of C60 Fullerene Nanoparticles in Simultaneous Exposure to Benzo[a]pyrene in a Molluscan Animal Model.

The hypothesis that C-60 fullerene nanoparticles (C-60) exert an antagonistic interactive effect on the toxicity of benzo[a] pyrene (BaP) has been supported by this investigation. Mussels were exposed to BaP (5, 50 & 100 mu g/L) and C-60 (C-60-1mg/L) separately and in combination. Both BaP and C-60 were shown to co-localize in the secondary lysosomes of the hepatopancreatic digestive cells in the digestive gland where they reduced lysosomal membrane stability (LMS) or increased membrane permeability, while BaP also induced increased lysosomal lipid and lipofuscin, indicative of oxidative cell injury and autophagic dysfunction. Combinations of BaP and C-60 showed antagonistic effects for lysosomal stability, mTORC1 (mechanistic target of rapamycin complex 1) inhibition and intralysosomal lipid (5 & 50 mu g/L BaP). The biomarker data (i.e., LMS, lysosomal lipidosis and lipofuscin accumulation; lysosomal/cell volume and dephosphorylation of mTORC1) were further analysed using multivariate statistics. Principal component and cluster analysis clearly indicated that BaP on its own was more injurious than in combination with C-60. Use of a network model that integrated the biomarker data for the cell pathophysiological processes, indicated that there were significant antagonistic interactions in network complexity (% connectance) at all BaP concentrations for the combined treatments. Loss of lysosomal membrane stability probably causes the release of intralysosomal iron and hydrolases into the cytosol, where iron can generate harmful reactive oxygen species (ROS). It was inferred that this adverse oxidative reaction induced by BaP was ameliorated in the combination treatments by the ROS scavenging property of intralysosomal C-60, thus limiting the injury to the lysosomalmembrane; and reducing the oxidative damage in the cytosol and to the nuclear DNA. The ROS scavenging by C-60, in combination with enhanced autophagic turnover of damaged cell constituents, appeared to have a cytoprotective effect against the toxic reaction to BaP in the combined treatments. (C) 2020 Elsevier B.V. All rights reserved.