Exosome-coated oxygen nanobubble-laden hydrogel augments intracellular delivery of exosomes for enhanced wound healing.
Xiaoxue HanChaimongkol SaengowLeah JuWen RenRandy H EwoldtJoseph Maria Kumar IrudayarajPublished in: Nature communications (2024)
Wound healing is an obvious clinical concern that can be hindered by inadequate angiogenesis, inflammation, and chronic hypoxia. While exosomes derived from adipose tissue-derived stem cells have shown promise in accelerating healing by carrying therapeutic growth factors and microRNAs, intracellular cargo delivery is compromised in hypoxic tissues due to activated hypoxia-induced endocytic recycling. To address this challenge, we have developed a strategy to coat oxygen nanobubbles with exosomes and incorporate them into a polyvinyl alcohol/gelatin hybrid hydrogel. This approach not only alleviates wound hypoxia but also offers an efficient means of delivering exosome-coated nanoparticles in hypoxic conditions. The self-healing properties of the hydrogel, along with its component, gelatin, aids in hemostasis, while its crosslinking bonds facilitate hydrogen peroxide decomposition, to ameliorate wound inflammation. Here, we show the potential of this multifunctional hydrogel for enhanced healing, promoting angiogenesis, facilitating exosome delivery, mitigating hypoxia, and inhibiting inflammation in a male rat full-thickness wound model.
Keyphrases
- wound healing
- stem cells
- hydrogen peroxide
- oxidative stress
- mesenchymal stem cells
- adipose tissue
- endothelial cells
- hyaluronic acid
- nitric oxide
- gene expression
- signaling pathway
- reactive oxygen species
- tissue engineering
- type diabetes
- bone regeneration
- mouse model
- metabolic syndrome
- risk assessment
- optical coherence tomography
- deep learning
- bone marrow
- vascular endothelial growth factor
- alcohol consumption