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. 2012 Jun 20;303(5):F757–F765. doi: 10.1152/ajprenal.00470.2011

Fig. 4.

Fig. 4.

Effect of TGF-β1 on the phosphorylation of ERK1/2 and JNK MAPK in HK-2 cells. Cells were exposed to TGF-β1 (10 ng/ml) for varying periods of time, cellular extracts were subjected to SDS-PAGE, and their protein blots were probed with various antibodies. A and B: TGF-β1 treatment increased ERK1/2 (A) and JNK (B) phosphorylation (p-ERK1/2 and p-JNK) in a dose-dependent manner with a peak effect around 60 min after exposure to the cytokine. No changes were observed in total (t-)ERK1/2 and JNK. The bar graphs (1 and 2) represent densities of the corresponding bands detected by immunoblot procedures relative to GAPDH. Values are expressed as means ± SE; n = 5. *P < 0.05 and **P < 0.01 compared with the control group.