C3G enhanced
promoter activity of CRE through the β2AR signaling
pathway. HEK293 cells were transiently co-transfected
with pGL4.29 and pcDNA3.1-β2AR then seeded into a
96-well plate. Transfected cells were treated with vehicle (0.1% DMSO,
shown as −), isoproterenol (10 μM, shown as Iso), or
C3G at the indicated concentrations for 24 h treatment. Luminescence
value corresponding to CRE promoter activity was measured using cell
lysates. Statistical analysis was conducted using one-way ANOVA (Tukey’s
test). Significance differences (****p < 0.0001,
**p < 0.01, *p < 0.05) versus
vehicle treatment group at cells co-transfected with pGL4.29 and pcDNA3.1-β2AR. Significant differences (####p < 0.0001,
##p < 0.01) versus vehicle treatment group at
cells transfected with pGL4.29. n = 5.