Objective: To study the promoting effect and mechanism of microRNA-126 (miR-126) overexpression in bone mesenchymal stem cells (BMSCs) on angiogenesis after skin flap transplantation. Methods: 24 SD rats were randomly divided into the observation group respectively in the free skin flap of 1 cm and 3 cm injected with 2 ml containing 1×106 miR-126 mimics transfected BMSCs, negative control group was transfected by injection of miR-126 mimics control of BMSCs and the blank control group was injected with phosphate buffer, with 8 rats in each group. The transient transfection was used to enhance the expression level of miR-126 in BMSCs. The protein levels of TNF-α, MIP-1α and VCAM-1 in the flap tissue were determined of the two groups, and the expression levels of TNF-α, MIP-1α and VCAM-1 mRNA in BMSCs were detected in the two groups. Results: The expression levels of TNF-α, MIP-1α and VCAM-1 in the tissue fluid of the observation group were significantly lower than those in the blank control group and the negative control group (all P<0.01), while the expression levels of TNF-α, MIP-1α and VCAM-1 in the negative control group were significantly lower than those in the blank control group (all P<0.01). The observation group after transfection in BMSCs, TNF-α MIP-1α and VCAM-1 mRNA relative expression were significantly lower than those in the blank control group and the negative controlgroup (all P<0.01), and the TNF-α MIP-1α and VCAM-1 mRNA relative expression in the negative control group were significantly lower than those in the blank control group (all P<0.01). Conclusion: After the transplantation of free flap, high expression of miR-126reduces the expression of TNF-α, MIP-1α and VCAM-1 mRNA, which can play the role of blocking vascular inflammation, activating angiogenesis induced by free flap glandular tissue, ultimately contribute to the neovascularization of flaps, and the survival of skin flaps. |
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