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. Author manuscript; available in PMC: 2019 Mar 1.
Published in final edited form as: Toxicology. 2018 Feb 7;396-397:54–67. doi: 10.1016/j.tox.2018.02.004

Figure 3. Quantification of anti-CD3/28-induced splenocyte proliferation of rats by treatment group and sex.

Figure 3

Male (A) and female (B) rats were administrated vehicle (VH, 0.3% aqueous carboxymethylcellulose), BPA or estrogen ethinyl estradiol (EE2) at the indicated dose level by oral gavage daily and sacrificed at postnatal day (PND) 6 month (A) and 1 year (B). Splenocytes were isolated and treated with anti-CD3/CD28 for 48 h after a 24 h pulse with [3H]-thymidine. Cells were harvested and quantified for [3H]-thymidine incorporation using a Tri-Carb 2100 TR scintillation counter, which is represented as counts per minute (CPM), Results are presented as mean ± SE. n = 4–10 rats/treatment group/sex. * p < 0.05, ** p < 0.01 when compared to respective vehicle control by a two way ANOVA with Dunnett’s posttest. For more details about VH-Ov, please see the Statistical Analysis section in the Materials and Methods.