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. 2017 Aug 24;6(6):878–888. doi: 10.1039/c7tx00126f

Fig. 4. Effects of supernatants from silica-treated macrophages on the expression of miR-29b in NIH-3T3 and MRC-5 cells. Supernatants from silica-treated macrophages suppressed the expression of miR-29b in fibroblast cells, as measured by qRT-PCR. (a) NIH-3T3 cells were cultured in DMEM (NC) or the supernatants collected from Raw264.7 cells exposed to 0, 25, 50, 100 or 200 μg mL–1 silica solution for 24 h. (b) MRC-5 cells were cultured in DMEM (NC) or the supernatants collected from Raw264.7 cells exposed to 0, 12.5, 25, 50 or 100 μg mL–1 silica solution for 24 h. There was a significant and dose-dependent decline in the level of miR-29b in NIH-3T3 (a). In MRC-5 (b), miR-29b levels showed a statistically significant decline in the silica 50 μg mL–1 group versus the silica 0 μg mL–1 group. The data are presented as the means ± SD (n = 3). The significance of differences was determined by ANOVA followed by the Dunnett's test; *p < 0.05 versus the NC group, **p < 0.01 versus the NC group, ^p < 0.05 versus the silica 0 group, ^^p < 0.01 versus the silica 0 group.

Fig. 4