• Morroniside accelerates skin wound healing by promoting re-epithelialization through enhanced epidermal stem cell proliferation.
• The compound acts via GLP-1R-mediated activation of PKA, PI3K/AKT, and ERK pathways, leading to increased β-catenin expression.
• Upregulation of β-catenin subsequently elevates cyclin D1, cyclin E1, and c-Myc, driving G1-to-S cell cycle progression in EpSCs.
• Topical application of morroniside increases EpSC proliferation and key signaling molecules in periwound tissue, suggesting clinical potential for wound treatment.
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