Nickel-Based Metal-Organic Frameworks Promote Diabetic Wound Healing via Scavenging Reactive Oxygen Species and Enhancing Angiogenesis.
Jia LiuZhongyin ChenHuan LiuSumei QinMingyi LiLin ShiCheng ZhouTao LiaoCao LiQiying LvMiaodeng LiuMeizhen ZouYan DengZheng WangLin WangPublished in: Small (Weinheim an der Bergstrasse, Germany) (2023)
Chronic diabetic wounds remain a worldwide challenge for both the clinic and research. Given the vicious circle of oxidative stress and inflammatory response as well as the impaired angiogenesis of the diabetic wound tissues, the wound healing process is disturbed and poorly responds to the current treatments. In this work, a nickel-based metal-organic framework (MOF, Ni-HHTP) with excellent antioxidant activity and proangiogenic function is developed to accelerate the healing process of chronic diabetic wounds. The Ni-HHTP can mimic the enzymatic catalytic activities of antioxidant enzymes to eliminate multi-types of reactive species through electron transfer reactions, which protects cells from oxidative stress-related damage. Moreover, this Ni-based MOF can promote cell migration and angiogenesis by activating transforming growth factor-β1 (TGF-β1) in vitro and reprogram macrophages to the anti-inflammatory phenotype. Importantly, Ni-HHTP effectively promotes the healing process of diabetic wounds by suppressing the inflammatory response and enhancing angiogenesis in vivo. This study reports a versatile and promising MOF-based nanozyme for diabetic wound healing, which may be extended in combination with other wound dressings to enhance the management of diabetic or non-healing wounds.
Keyphrases
- wound healing
- metal organic framework
- oxidative stress
- inflammatory response
- transforming growth factor
- anti inflammatory
- gene expression
- reactive oxygen species
- type diabetes
- emergency department
- cell migration
- endothelial cells
- dna damage
- primary care
- nitric oxide
- epithelial mesenchymal transition
- immune response
- hydrogen peroxide
- drug induced
- carbon nanotubes
- toll like receptor
- induced apoptosis
- endoplasmic reticulum stress
- reduced graphene oxide