Comparison of In Vitro Proliferative Response of Thymocytes and Splenic T Cells Between wt and hSCF 220 Mice
Genotype . | Treatment . | Thymocytes . | Splenocytes . |
---|---|---|---|
wt | PBS | 0.33 ± 0.03 | 0.26 ± 0.006 |
Anti-CD3 MoAb | 0.78 ± 0.14-150 | 0.60 ± 0.064-150 | |
hSCF 220 | PBS | 0.27 ± 0.02 | 0.36 ± 0.01 |
Anti-CD3 MoAb | 0.39 ± 0.04 | 0.76 ± 0.14-150 |
Genotype . | Treatment . | Thymocytes . | Splenocytes . |
---|---|---|---|
wt | PBS | 0.33 ± 0.03 | 0.26 ± 0.006 |
Anti-CD3 MoAb | 0.78 ± 0.14-150 | 0.60 ± 0.064-150 | |
hSCF 220 | PBS | 0.27 ± 0.02 | 0.36 ± 0.01 |
Anti-CD3 MoAb | 0.39 ± 0.04 | 0.76 ± 0.14-150 |
In vitro proliferation on thymocytes and splenic T cells from wt and hSCF 220 mice was performed as described in Materials and Methods. Thymoctyes and splenocytes were cultured in the presence of 10 μg/mL of anti-CD3 MoAb, and their proliferation monitored for 3 days. Proliferation was determined by measuring the optical density (OD) at 405 nm using an Elisa plate reader. At least three mice were examined per group. Data represent the mean ± SEM for each group from two separate experiments.
P < .05 anti-CD3 v PBS control for wt thymocytes. *P < .01 anti-CD3 v PBS control for wt splenocytes and *P < .05 for hSCF 220 splenocytes. Anti-CD3 MoAb mediated proliferation of splenocytes from wt and hSCF 220 was not statistically different (P = .2).