Table 4.

Comparison of In Vitro Proliferative Response of Thymocytes and Splenic T Cells Between wt and hSCF 220 Mice

GenotypeTreatmentThymocytesSplenocytes
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 
GenotypeTreatmentThymocytesSplenocytes
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.

F4-150

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).

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