Salvianolic Acid B Inhibits ERK and p38 MAPK Signaling in TGF-1-Stimulated Human Hepatic Stellate Cell Line (LX-2) via Distinct Pathways
Figure 3
The effects of SA-B on ERK signaling via inhibition of p38 MAPK and Smad signaling. (a) MEK phosphorylation in LX-2 cells. The levels of phosphorylated MEK protein were determined by Western blot using anti-phospho-MEK antibodies. The levels of total MEK protein were determined by Western blot using anti-MEK antibodies. Quantification of the intensity of bands calibrated to the intensity of total protein bands (means ± SD). ###Significant difference versus Control, Negative control, and SRV4 (); **Significant difference versus TGF (); ▲▲▲Significant difference versus SM4 + TGF, SM4 + TGF + SB, and TGF + SA-B + SB (). (b) α-SMA levels in LX-2. The levels of α-SMA protein were determined using anti-α-SMA antibodies. Blotting with anti-GAPDH antibodies was conducted as a protein loading control. ##Significant difference versus Control, Negative control and SRV4 (, ); ▲▲Significant difference versus TGF (); ⋄⋄Significant difference versus SM4 + TGF (); Significant difference versus SM4 + TGF (); ***Significant difference versus SM4 + TGF + SB, SM4 + TGF + SA-B, and TGF + SA-B + SB (). (c) Col. I level in LX-2. The levels of Col. I protein were determined by Western blot using anti-Col. I antibodies. Blotting with anti-GAPDH antibodies was conducted as a protein loading control. ##Significant difference versus Control, Negative control, and SRV4 (); ▲▲Significant difference versus TGF (); ◊Significant difference versus SM4 + TGF (); ◊◊Significant difference versus SM4 + TGF (); **Significant difference versus SM4 + TGF + SB, SM4 + TGF + SA-B, and TGF + SA-B + SB .