Mechanistic Differences in Cell Death Responses to Metal‐Based Engineered Nanomaterials in Kupffer Cells and Hepatocytes

The mononuclear phagocyte system in the liver is a frequent target for nanoparticles (NPs). A toxicological profiling of metal‐based NPs is performed in Kupffer cell (KC) and hepatocyte cell lines. Sixteen NPs are provided by the Nanomaterial Health Implications Research Consortium of the National Institute of Environmental Health Sciences to study the toxicological effects in KUP5 (KC) and Hepa 1–6 cells. Five NPs (Ag, CuO, ZnO, SiO2, and V2O5) exhibit cytotoxicity in both cell types, while SiO2 and V2O5 induce IL‐1β production in KC. Ag, CuO, and ZnO induced caspase 3 generated apoptosis in both cell types is accompanied by ion shedding and generation of mitochondrial reactive oxygen species (ROS) in both cell types. However, the cell death response to SiO2 in KC differs by inducing pyroptosis as a result of potassium efflux, caspase 1 activation, NLRP3 inflammasome assembly, IL‐1β release, and cleavage of gasdermin‐D. This releases pore‐performing peptide fragments responsible for pyroptotic cell swelling. Interestingly, although V2O5 induces IL‐1β release and delays caspase 1 activation by vanadium ion interference in membrane Na+/K+ adenosine triphosphate (ATP)ase activity, the major cell death mechanism in KC (and Hepa 1–6) is caspase 3 mediated apoptosis. These findings improve the understanding of the mechanisms of metal‐based engineered nanomaterial (ENM) toxicity in liver cells toward comprehensive safety evaluation. Sixteen metal‐based nanoparticles are tested for cytotoxicity in Kupffer cells (KC) and hepatocytes. Ag, CuO, ZnO induce caspase 3 mediated apoptosis in both cells. However, SiO2 induces caspase 1 mediated pyroptosis in KC. Although V2O5 induces caspase 1 activation in KC, caspase 3 mediated apoptosis is induced rather than pyroptosis due to delayed caspase 1 activation by vanadium ion interference in membrane Na+/K+ adenosine triphosphate (ATP)ase activity.