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. 2018 Apr 23;137(17):1824–1841. doi: 10.1161/CIRCULATIONAHA.117.027799

Figure 3.

Figure 3.

miR-22 modulates VSMC proliferation and migration. VSMCs were transfected with miR-22 mimics, miR-22 inhibitor, or respective negative control miR (miRNA ctrl), followed by 24 hours of serum starvation. Subsequently, cells were treated with vehicle control (Ctrl), PDGF-BB (10 ng/mL), or serum (20%) for 48 hours and analyzed. A, RT-qPCR analysis confirmed miR-22 overexpression in VSMCs transfected with miR-22 mimics on PDGF-BB and serum treatment. B, RT-qPCR analysis confirmed that miR-22 expression was significantly inhibited in VSMCs transfected with miR-22 inhibitor in all treatments. C, BrdU assays revealed significantly decreased absorbance of VSMCs transfected with miR-22 mimics in all treatments, indicating decreased proliferation. D, Transwell migration assays showed significantly decreased migration of VSMCs transfected with miR-22 mimics under both PDGF-BB and serum stimulation. E, BrdU assays revealed significantly increased absorbance and therefore proliferation of VSMCs transfected with the miR-22 inhibitor on PDGF-BB and serum treatment. F, Transwell migration assays showed significantly increased migration of VSMCs transfected with the miR-22 inhibitor under both PDGF-BB and serum stimulation. Note: No or very few migrated cells were observed without cell chemoattractant in transwell migration assays; therefore, no control treatment is shown. Data and error bars represent the mean±SEM (n=3 in A; 4 in B, C, and E; or 5 in D and F). *P<0.05 (versus miRNA ctrl). #P<0.05 (versus Ctrl). BrdU indicates bromodeoxyuridine; miR-22, microRNA-22; PDGF-BB, platelet-derived growth factor BB; RT-qPCR, reverse transcription quantitative polymerase chain reaction; and VSMC, vascular smooth muscle cell.