Figure 2
Figure 2. Selection of EBV-CTLs with a silenced FKBP12 occurs in the presence of FK506. EBV-CTLs were transduced with either the pSUPER.eGFP vector encoding the irrelevant siRNA (irr-siRNA) or pSUPER.eGFP encoding siRNA4. (A) GFP expression (as measure of transduction) of irr-siRNA+ (top plots) and siRNA4+ (bottom plots) EBV-CTLs stimulated with irradiated EBV-LCLs in the presence of IL-2 (20 U/mL) and FK506 (5 ng/mL) in a representative donor. The plots show a progressive increase of GFP+ cells for siRNA4+ CTLs, whereas the percentage of GFP+ cells is stable for irr-siRNA+ CTLs. (B) The data for the percentage of GFP+ cells for 6 CTL lines. Bars represent mean ± SD. Shown is the percentage of GFP+ cells after the 4th, 7th, and 11th stimulations, which significantly increased over time only for siRNA4+ EBV-CTLs, whereas it remained stable for irr-siRNA+ EBV-CTLs. (C) The MFI of GFP+ cells significantly increased in siRNA4+ EBV-CTLs compared with irr-siRNA+ cells when cells were maintained in culture in the presence of FK506. Bars represent mean ± SD for 6 CTL lines. (D) The expression of FKBP12 in NT and irr-siRNA+ EBV-CTLs and in siRNA4+ EBV-CTLs after 5 weeks in culture in the absence or in the presence of FK506, as assessed by WB. FKBP12 is completely undetectable by WB in siRNA4+ EBV-CTLs cultured in the presence of FK506.

Selection of EBV-CTLs with a silenced FKBP12 occurs in the presence of FK506. EBV-CTLs were transduced with either the pSUPER.eGFP vector encoding the irrelevant siRNA (irr-siRNA) or pSUPER.eGFP encoding siRNA4. (A) GFP expression (as measure of transduction) of irr-siRNA+ (top plots) and siRNA4+ (bottom plots) EBV-CTLs stimulated with irradiated EBV-LCLs in the presence of IL-2 (20 U/mL) and FK506 (5 ng/mL) in a representative donor. The plots show a progressive increase of GFP+ cells for siRNA4+ CTLs, whereas the percentage of GFP+ cells is stable for irr-siRNA+ CTLs. (B) The data for the percentage of GFP+ cells for 6 CTL lines. Bars represent mean ± SD. Shown is the percentage of GFP+ cells after the 4th, 7th, and 11th stimulations, which significantly increased over time only for siRNA4+ EBV-CTLs, whereas it remained stable for irr-siRNA+ EBV-CTLs. (C) The MFI of GFP+ cells significantly increased in siRNA4+ EBV-CTLs compared with irr-siRNA+ cells when cells were maintained in culture in the presence of FK506. Bars represent mean ± SD for 6 CTL lines. (D) The expression of FKBP12 in NT and irr-siRNA+ EBV-CTLs and in siRNA4+ EBV-CTLs after 5 weeks in culture in the absence or in the presence of FK506, as assessed by WB. FKBP12 is completely undetectable by WB in siRNA4+ EBV-CTLs cultured in the presence of FK506.

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