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Fig. 1 PEG impact on MC3T3-E1 and hFOB cell proliferation, apoptosis, and viability. A MC3T3-E1 and B hFOB cells were stimulated with PEG at 1 and 10 μg/ml for 48 h. Subsequently, cells were incubated with BrdU for 2 h. Untreated cells were used as control (UT). C, D MC3T3-E1 and hFOB cells were treated with PEG 1 and 10 μg/ml for 48 h. Apoptosis was detected by measuring Caspase-9 enzymatic activity. Values represent the mean ± SD of three experiments. Statistical analysis was performed with One-Way ANOVA followed by Dunnett’s post-hoc test
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Full text @ J. Endocrinol. Invest.