• ADSC-Exos accelerate wound healing by promoting M2 macrophage polarization, reducing inflammation, and enhancing collagen deposition and angiogenesis.
• IL-33 is identified as a key mediator in ADSC-Exos-induced wound healing, with its release from macrophages driving keratinocyte proliferation and epithelialization.
• The Wnt/β-catenin signaling pathway is activated by IL-33, linking ADSC-Exos to enhanced keratinocyte function.
• ADSC-Exos offer a promising cell-free therapeutic strategy for skin repair, potentially overcoming limitations of direct MSC transplantation.
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