Figure 4
Figure 4. IL-2R/IL-2 signaling regulates hTERT promoter expression. (A) IL-2 was withdrawn from 1185 and LAF cells for 4 or 24 (overnight [O/N]) hours, followed by hTERT RNA expression by RT-PCR. (B) LAF cells were cultured in the absence of IL-2 for 4 hours, and subsequently pulsed with IL-2 for 4 and 24 hours before hTERT RT-PCR analysis. Cells grown continuously in IL-2 media served as a control (first lane). (C) 1185 cells were treated with actinomycin D (5 μg/mL) in the presence or absence of IL-2 for 0, 1, 2, and 4 hours. RNA was extracted and analyzed for hTERT expression by RT-PCR. (A-C) GAPDH was used as an amplification control.

IL-2R/IL-2 signaling regulates hTERT promoter expression. (A) IL-2 was withdrawn from 1185 and LAF cells for 4 or 24 (overnight [O/N]) hours, followed by hTERT RNA expression by RT-PCR. (B) LAF cells were cultured in the absence of IL-2 for 4 hours, and subsequently pulsed with IL-2 for 4 and 24 hours before hTERT RT-PCR analysis. Cells grown continuously in IL-2 media served as a control (first lane). (C) 1185 cells were treated with actinomycin D (5 μg/mL) in the presence or absence of IL-2 for 0, 1, 2, and 4 hours. RNA was extracted and analyzed for hTERT expression by RT-PCR. (A-C) GAPDH was used as an amplification control.

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