Three-Step Depletion Strategy of Glutathione: Tunable Metal-Organic-Framework-Engineered Nanozymes for Driving Oxidative/Nitrative Stress to Maximize Ferroptosis Therapy.
Wenting LiShikai LiuHe DingRuoxi ZhaoPengyu ZangSiyi LiLinyang FangRumin LiManjie ZhangPiaoping YangPublished in: Nano letters (2024)
Ferroptosis is a novel type of nonapoptotic programmed cell death involving the accumulation of lipid peroxidation (LPO) to a lethal threshold. Herein, we propose tunable zeolitic imidazolate framework (ZIFs)-engineered biodegradable nanozymes for ferroptosis mediated by both reactive oxygen species (ROS) and nitrogen species (RNS). l-Arginine is utilized as an exogenous nitric oxide donor and loaded into hollow ZIFs@MnO 2 artificial nanozymes, which are formed by etching ZIFs with potassium permanganate and simultaneously generating a MnO 2 shell in situ . The constructed nanozymes with multienzyme-like activities including peroxidase, oxidase, and catalase can release satisfactory ROS and RNS through a cascade reaction, consequently promoting the accumulation of LPO. Furthermore, it can improve the efficiency of ferroptosis through a three-step strategy of glutathione (GSH) depletion; that is, the outer MnO 2 layer consumes GSH under slightly acidic conditions and RNS downregulates SLC7A11 and glutathione reductase, thus directly inhibiting GSH biosynthesis and indirectly preventing GSH regeneration.
Keyphrases
- cell death
- metal organic framework
- reactive oxygen species
- nitric oxide
- fluorescent probe
- drug delivery
- hydrogen peroxide
- stem cells
- dna damage
- nitric oxide synthase
- wound healing
- cancer therapy
- stress induced
- mesenchymal stem cells
- oxidative stress
- light emitting
- genetic diversity
- cell therapy
- simultaneous determination
- cell wall