Figure 4
From: Safety of Nonporous Silica Nanoparticles in Human Corneal Endothelial Cells

Effect of SiNPs on the autophagy and mTOR pathway of HCECs. (A) The expression levels for the autophagy signal, the LC3A/B proteins, and the levels of mTOR were detected by Western blot analysis in HCECs treated with SiNPs for 24 h. For the LC3A/B, the inactive is I form and the active is II form. For the mTOR, the active form is phosphorylated mTOR (p-mTOR). (B) The relative densitometric analyses of Western blots showed the dose-dependently increased expression of LC3A/B II form with high concentrations of SiNPs (50, 100, and 150 nm) added. (C) The mTOR signal activation did not significantly change with the treatment of SiNPs at a concentration of up to 100 μg/mL. Relative densitometry was calculated as a fold change from the control, and all values (mean ± SEM) were obtained from three independent experiments; each independent experiment was performed in triplicate (*p < 0.05, **p < 0.01, ***p < 0.001).