Copper oxide nanoparticles trigger macrophage cell death with misfolding of Cu/Zn superoxide dismutase 1 (SOD1)

• Published in: Particle and fibre toxicology 2022-05, Vol.19 (1), p.33-33, Article 33
• Main Authors: Gupta, Govind, Cappellini, Francesca, Farcal, Lucian, Gornati, Rosalba, Bernardini, Giovanni, Fadeel, Bengt
• Format: Article
• Language: English
• Subjects: Apoptosis; Assaying; Autophagy; Caspase; Caspase inhibitors; Cell culture; Cell death; Chelation; Circular dichroism; Confocal microscopy; Copper; Copper chloride; Copper oxide; Copper oxide nanoparticles; Copper oxides; Cuprite; Cytotoxicity; Depletion; Deposition; Dichroism; Environmental aspects; Exposure; Flow cytometry; Genetic aspects; Glutathione; Health aspects; Heat shock proteins; Inductively coupled plasma mass spectrometry; Lysosomes; Macrophages; Mass spectrometry; Mass spectroscopy; Medicin och hälsovetenskap; Membrane potential; Membrane proteins; Microscopy; Mitochondria; Mortality; Nanomaterials; Nanoparticles; Oxidative stress; Phagocytosis; Proteasomes; Protein misfolding; Proteins; Reagents; Superoxide dismutase; Toxicity; Translocation; Transmission electron microscopy; Wood preservatives; Zinc oxide
• ISSN: 1743-8977; 1743-8977
• DOI: 10.1186/s12989-022-00467-w

Copper oxide (CuO) nanoparticles (NPs) are known to trigger cytotoxicity in a variety of cell models, but the mechanism of cell death remains unknown. Here we addressed the mechanism of cytotoxicity in macrophages exposed to CuO NPs versus copper chloride (CuCl ). The mouse macrophage cell line RAW264.7 was used as an in vitro model. Particle uptake and the cellular dose of Cu were investigated by transmission electron microscopy (TEM) and inductively coupled plasma mass spectrometry (ICP-MS), respectively. The deposition of Cu in lysosomes isolated from macrophages was also determined by ICP-MS. Cell viability (metabolic activity) was assessed using the Alamar Blue assay, and oxidative stress was monitored by a variety of methods including a luminescence-based assay for cellular glutathione (GSH), and flow cytometry-based detection of mitochondrial superoxide and mitochondrial membrane potential. Protein aggregation was determined by confocal microscopy using an aggresome-specific dye and protein misfolding was determined by circular dichroism (CD) spectroscopy. Lastly, proteasome activity was investigated using a fluorometric assay. We observed rapid cellular uptake of CuO NPs in macrophages with deposition in lysosomes. CuO NP-elicited cell death was characterized by mitochondrial swelling with signs of oxidative stress including the production of mitochondrial superoxide and cellular depletion of GSH. We also observed a dose-dependent accumulation of polyubiquitinated proteins and loss of proteasomal function in CuO NP-exposed cells, and we could demonstrate misfolding and mitochondrial translocation of superoxide dismutase 1 (SOD1), a Cu/Zn-dependent enzyme that plays a pivotal role in the defense against oxidative stress. The chelation of copper ions using tetrathiomolybdate (TTM) prevented cell death whereas inhibition of the cellular SOD1 chaperone aggravated toxicity. Moreover, CuO NP-triggered cell death was insensitive to the pan-caspase inhibitor, zVAD-fmk, and to wortmannin, an inhibitor of autophagy, implying that this was a non-apoptotic cell death. ZnO NPs, on the other hand, triggered autophagic cell death. CuO NPs undergo dissolution in lysosomes leading to copper-dependent macrophage cell death characterized by protein misfolding and proteasomal insufficiency. Specifically, we present novel evidence for Cu-induced SOD1 misfolding which accords with the pronounced oxidative stress observed in CuO NP-exposed macrophages. These results are