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. 2017 Jun 21;313(3):C285–C294. doi: 10.1152/ajpcell.00073.2017

Fig. 1.

Fig. 1.

Oxidative stress downregulates protein arginine methyltransferase 4 (PRMT4) protein stability. A: time course study of H2O2 in murine lung epithelial (MLE12) cells. MLE12 cells were treated with 200 μM H2O2 for different time durations. The cell lysates were analyzed with PRMT4 and glycogen synthase kinase 3β (GSK-3β) immunoblotting, and β-actin was used as a loading control. B: the densitometry results of A were plotted. C: concentration course study of H2O2 in MLE12 cells. MLE12 cells were treated with diverse concentration of H2O2 for 4 h. PRMT4, GSK-3β, and β-actin immunoblotting was conducted. D: the densitometry results of C were plotted. E: MLE12 cells were treated with 200 μM H2O2 for 4 h, and total RNA was isolated and analyzed with quantitative RT-PCR. Results are representative of 3 independent experiments. *P < 0.05 or **P ≤ 0.01 vs. corresponding control.