CuCo 2 O 4 Nanoflowers with Multiple Enzyme Activities for Treating Bacterium-Infected Wounds via Cuproptosis-like Death.
Wenqi WangYuyu CuiXiaolong WeiYing ZangXulin ChenLiang ChengXian-Wen WangPublished in: ACS nano (2024)
Nanozyme-driven catalytic therapy provides a promising treatment strategy for bacterial biofilm-infected wounds. However, the single functionality and limited catalytic efficiency of nanozyme-based materials often restrict the effectiveness of wound infection treatment. In this study, CuCo 2 O 4 nanoflowers with multiple enzymatic activities were prepared for antibacterial/antibiofilm treatment by cuproptosis-like death. CuCo 2 O 4 exhibited peroxidase-like (POD-like) and oxidase-like (OXD-like) dual enzyme activities that generated large amounts of •OH and O 2 •- . Moreover, the glutathione peroxidase-like (GSH-Px-like) activity of CuCo 2 O 4 was able to reduce the overexpression of GSH in the wound microenvironment, enhancing the therapeutic effects of reactive oxygen species (ROS). The morphology of CuCo 2 O 4 was modified using a hydrothermal method with PEG4000 as the solvent, resulting in the exposure of more active center sites and a significant improvement in enzyme catalytic activity. The in vitro results demonstrated the pronounced disruption effect of CuCo 2 O 4 on biofilms formed by bacteria. In vivo, CuCo 2 O 4 significantly promoted angiogenesis, collagen deposition, and cell proliferation. Transcriptome sequencing revealed that elevated ROS levels in bacteria led to cell membrane damage and metabolic disruption. In addition, Cu 2+ overload in bacteria induces lipid peroxidation accumulation and disrupts the respiratory chain and tricarboxylic acid (TCA) cycle, ultimately leading to bacterial cuproptosis-like death. This therapeutic strategy, which combines the synergistic effects of multiple enzyme-like activities with cuproptosis-like death, provides an approach for treating biofilm infections.
Keyphrases
- reactive oxygen species
- cell proliferation
- wound healing
- pseudomonas aeruginosa
- hydrogen peroxide
- single cell
- candida albicans
- staphylococcus aureus
- stem cells
- randomized controlled trial
- dna damage
- cell death
- oxidative stress
- combination therapy
- vascular endothelial growth factor
- cell cycle
- systematic review
- nitric oxide
- risk assessment
- bone marrow
- mesenchymal stem cells
- signaling pathway
- rna seq
- cancer therapy
- biofilm formation
- escherichia coli
- pi k akt