• MSCs effectively reverse airway remodeling in a chronic HDM-induced asthma mouse model, closely mimicking clinical asthma.
• MSC treatment inhibits the HIF-1 signaling pathway and downregulates Timp1 and Wnt2b expression, which are key players in fibrosis.
• STRING and western blot analyses confirm a reciprocal interaction between Timp1 and Wnt2b, suggesting a coordinated axis.
• Overexpression of Timp1 in MSCs abolishes their therapeutic effect, proving that MSCs act via inhibiting the Timp1-Wnt2b axis.
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