炎症
表观遗传学
再生(生物学)
慢性伤口
伤口愈合
医学
细胞生物学
癌症研究
炎症反应
染色质
组织修复
糖尿病
染色质重塑
自愈水凝胶
细胞凋亡
调解人
化学
氧化应激
再生医学
免疫学
生物
活性氧
生物信息学
促炎细胞因子
作者
Amal George Kurian,J Hong Park,Shanika Karunasagara,Archita Gupta,Shreyas Kumar Jain,Tanza Baby,Ueon Sang Shin,Sak Lee,Buuvee Bayarkhangai,Rajendra K. Singh,Jung‐Hwan Lee,Kam W. Leong,Hae-Won Kim
标识
DOI:10.1038/s41467-026-72968-7
摘要
Chronic diabetic wounds present a critical clinical challenge due to persistent inflammation and compromised healing. Here, we report a sprayable nanozyme hydrogel that epigenetically remodels macrophages (Mφ) to suppress inflammation and coordinate regeneration. Ultrasmall copper-based nanozymes (CuNZ, ~4 nm) synthesized via an eco-friendly one-pot method demonstrated potent multi-radical scavenging activity. When integrated into gelatin methacryloyl (Gel), CuNZ@Gel exhibited sprayability, conformal skin coverage, and storage stability, offering potential for clinical translation. Notably, the nanozyme hydrogel induced distinct epigenetic modifications in Mφ by remodeling chromatin accessibility, thereby shifting gene expression from a pro-inflammatory to an anti-inflammatory profile. This epigenetic modulation sustained under oxidative stress, actively suppressing inflammation while facilitating regenerative responses. In rat diabetic wound models, CuNZ@Gel significantly accelerated healing through its coordinated antioxidant, anti-inflammatory, and pro-regenerative actions. Unlike conventional passive dressings, this sprayable nanozyme hydrogel proactively remodels the wound microenvironment via epigenetic control of inflammation, providing a promising therapeutic strategy for managing chronic diabetic wounds and inflammatory skin complications.
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