ACS Applied Materials & Interfaces · 2023 · 28 citations · 28 references
Life SciencesBiochemistryNephrologyInflammationNanobiotechnologyNanomaterialsAntioxidant DefenseInorganic NanoparticlesNanomedicineNanoparticle DesignOxidative Stress In InflammationRenal IschemiaAcute Inflammatory ResponseAntioxidant PropertiesInflammatory Responses To NanoparticlesIron Oxide NanoparticlesIron-dependent Lipid PeroxidationIschemia-reperfusion Oxidative InjuryKidney DiseasesOxidative Stress Injury
Ischemia/reperfusion (I/R) injury causes excessive oxidative events and initiates destructive inflammatory responses, and it is an important promoter to the pathology of various pathema states. Ferroptosis is an iron-dependent type of nonapoptotic cell death accompanied by the accumulation of membrane lipid peroxide and consumption of polyunsaturated fatty acid, and it plays a key role in I/R injury diseases. Moreover, the excessive production of inflammatory cytokines contributes to the development of acute kidney injury. Here, we reported neutrophil membrane-coated copper-based nanoparticles (N–Cu 5.4 O@DFO NPs) for I/R kidney injury treatment. The highly biocompatible and stable N–Cu 5.4 O@DFO NPs showed excellent antioxidant and iron ion scavenging abilities in vitro . Our finding showed that the N–Cu 5.4 O@DFO NPs strategy could significantly accumulate in the inflammatory kidney, reduce oxidative damage events and inflammatory response, and finally achieve synergistic therapy against renal I/R injury. This work promotes the development of nanoantioxidant agents with multiple antioxidant properties for the therapy of other I/R injury diseases.
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Synchronized renal tubular cell death involves ferroptosis
Andreas Linkermann, Rachid Skouta, Nina Himmerkus et al. · Proceedings of the National Academy of Sciences · 2014 · 1.1K citations · Full text
Medicine, Cell Biology, Nephrology +16