Fig. 10From: Hypoxic mesenchymal stem cell-derived exosomes promote the survival of skin flaps after ischaemia–reperfusion injury via mTOR/ULK1/FUNDC1 pathwaysSchematic Diagram: Hypo-Exo, carrying miR-421-3p, activates autophagy by targeting mTOR and upregulating the expression of phosphorylated ULK1 and FUNDC1. This in turn mitigates the release of inflammatory factors in the skin flap, reduces ROS generation, counteracts cell apoptosis, and protects blood vessels, ultimately promoting the survival of ischemia–reperfusion flapsBack to article page