Fig. 4: MiR-494 overexpression inhibits angiogenesis and osteogenic differentiation.

A Expression levels of miR-494 were evaluated by qRT-PCR. B–E MC3T3-E1 cells were transfected with miR-494 mimics or NC mimics. B Activity of ALP was detected using an ALP detection kit. C ARS assay was performed to assess mineralized nodules. D The protein expression of RUNX2 and OSX was determined by western blotting. E VEGFA concentrations in the supernatant were determined by ELISA. F–H HUVECs were treated with the supernatant from MC3T3-E1 cells transfected with miR-494 mimics or NC mimics. F Proliferation of HUVECs was detected by MTT assay. G Migration of HUVECs was measured using Transwell assays. H Tube size and numbers of HUVECs were observed under a microscope and imaged. Data are the mean ± SD for three separate experiments. The P value was determined by ANOVA following Tukey’s post hoc test and Student’s t-test. *P < 0.05, **P < 0.01, and ***P < 0.001.