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©The Author(s) 2025.
World J Diabetes. Apr 15, 2025; 16(4): 100113
Published online Apr 15, 2025. doi: 10.4239/wjd.v16.i4.100113
Published online Apr 15, 2025. doi: 10.4239/wjd.v16.i4.100113
Figure 4 MicroRNA-122-5p reduced vascular endothelial growth and delayed fibrosis during the transition from the inflammatory phase to the proliferative phase.
A and B: Levels of vascular endothelial growth factor (VEGF), fibronectin (FN) 1, and α-smooth muscle actin (α-SMA) in wound tissues of mice after 14 days were detected using immunohistochemistry (20 ×); C: The expression of VEGF, FN1, and α-SMA in wound tissues of mice was assessed using quantitative real-time polymerase chain reaction; D and E: Expressions of VEGF, FN1, and α-SMA proteins were tested in wound tissues (n = 3); F and G: Expressions of VEGF, FN1, and α-SMA proteins were tested in NIH3T3 cells in different groups (n = 3). aP < 0.05. bP < 0.01. cP < 0.001. DU: Diabetic ulcer; miR: MicroRNA; AAVDJ: Adeno-associated virus-DJ; SMA: Smooth muscle actin; VEGF: Vascular endothelial growth factor; FN: Fibronectin; NC: Normal control.
- Citation: Yuan MJ, Huang HC, Shi HS, Hu XM, Zhao Z, Chen YQ, Fan WJ, Sun J, Liu GB. MicroRNA-122-5p is upregulated in diabetic foot ulcers and decelerates the transition from the inflammatory to the proliferative stage. World J Diabetes 2025; 16(4): 100113
- URL: https://www.wjgnet.com/1948-9358/full/v16/i4/100113.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i4.100113