Fig. 8.
Fig. 8. Retrovirus-mediated expression of Stat5b restores Th2 cell differentiation in Stat5a−/−CD4+ T cells. / Purified splenic CD4+ T cells from DO10+Stat5a−/− mice were stimulated with platebound anti-CD3 mAb and anti-CD28 mAb for 48 hours in Th2-polarizing condition. Activated T cells were then infected with retroviruses of pMX-Stat5a-IRES-GFP, pMX-Stat5b-IRES-GFP, or pMX-IRES-GFP (as a negative control) as described in “Materials and methods.” Cells were cultured with IL-2 for another 60 hours and then restimulated with platebound anti-CD3 antibody for 6 hours. Intracellular cytokine profiles for IL-4 versus IFN-γ were evaluated on infected CD4+ T cells (GFP+CD4+cells). Shown is representative intracellular cytokine staining from 4 independent experiments.

Retrovirus-mediated expression of Stat5b restores Th2 cell differentiation in Stat5a−/−CD4+ T cells.

Purified splenic CD4+ T cells from DO10+Stat5a−/− mice were stimulated with platebound anti-CD3 mAb and anti-CD28 mAb for 48 hours in Th2-polarizing condition. Activated T cells were then infected with retroviruses of pMX-Stat5a-IRES-GFP, pMX-Stat5b-IRES-GFP, or pMX-IRES-GFP (as a negative control) as described in “Materials and methods.” Cells were cultured with IL-2 for another 60 hours and then restimulated with platebound anti-CD3 antibody for 6 hours. Intracellular cytokine profiles for IL-4 versus IFN-γ were evaluated on infected CD4+ T cells (GFP+CD4+cells). Shown is representative intracellular cytokine staining from 4 independent experiments.

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