Fig. 11.
Fig. 11. TSA and NaB affect NF-κB and p38 MAPK signaling pathways in RAW-D cells. / . (A) TSA or NaB suppresses the nuclear translocation of NF-κB p65 in RAW-D cells stimulated with TNF-α. RAW-D cells were treated without or with TSA (100 nM) or NaB (1 mM) for 24 hours, followed by treatment with TNF-α for 30 minutes. Nuclear extracts were prepared and analyzed by Western blotting using NF-κB p65 antibody. (B) TSA or NaB suppresses activation of p38 MAPK in RAW-D cells stimulated with sRANKL. RAW-D cells were preincubated with or without TSA (100 nM) or NaB (1 mM) for 24 hours and stimulated with sRANKL (100 ng/mL) for 30 minutes. Whole-cell lysates were prepared and analyzed by Western blotting using phosphorylated p38 MAPK antibody. The bottom lane indicates equal loading of protein probed for actin antibody.

TSA and NaB affect NF-κB and p38 MAPK signaling pathways in RAW-D cells

. (A) TSA or NaB suppresses the nuclear translocation of NF-κB p65 in RAW-D cells stimulated with TNF-α. RAW-D cells were treated without or with TSA (100 nM) or NaB (1 mM) for 24 hours, followed by treatment with TNF-α for 30 minutes. Nuclear extracts were prepared and analyzed by Western blotting using NF-κB p65 antibody. (B) TSA or NaB suppresses activation of p38 MAPK in RAW-D cells stimulated with sRANKL. RAW-D cells were preincubated with or without TSA (100 nM) or NaB (1 mM) for 24 hours and stimulated with sRANKL (100 ng/mL) for 30 minutes. Whole-cell lysates were prepared and analyzed by Western blotting using phosphorylated p38 MAPK antibody. The bottom lane indicates equal loading of protein probed for actin antibody.

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