Table 1.

Effect of UV Irradiation on the Viability of FDC-P1 Cells Expressing or Not Expressing mcl-1

Transfectant CloneExpression of mcl-1*% Viable Cells
UV Irradiation
+
Experiment I 
8.5-MAMneo (−Dex) − 99 ± 0.2 42 ± 3.3 
8.5-MAMneo (+Dex) − 99 ± 0.2 44 ± 0.3 
7.5-MAMmcl-1 (−Dex) − 99 ± 0.7 38 ± 0.6 
7.5-MAMmcl-1 (+Dex) 99 ± 0.3 76 ± 3.1 
Experiment II 
V1-CMVneo − 99 ± 0.4 13 ± 3.1 
V2-CMVneo − 99 ± 0.1 8 ± 2.8 
S3-CMVmcl-1 98 ± 0.7 60 ± 4.8 
S8-CMVmcl-1 98 ± 0.7 44 ± 7.6 
Transfectant CloneExpression of mcl-1*% Viable Cells
UV Irradiation
+
Experiment I 
8.5-MAMneo (−Dex) − 99 ± 0.2 42 ± 3.3 
8.5-MAMneo (+Dex) − 99 ± 0.2 44 ± 0.3 
7.5-MAMmcl-1 (−Dex) − 99 ± 0.7 38 ± 0.6 
7.5-MAMmcl-1 (+Dex) 99 ± 0.3 76 ± 3.1 
Experiment II 
V1-CMVneo − 99 ± 0.4 13 ± 3.1 
V2-CMVneo − 99 ± 0.1 8 ± 2.8 
S3-CMVmcl-1 98 ± 0.7 60 ± 4.8 
S8-CMVmcl-1 98 ± 0.7 44 ± 7.6 

In experiment I, the indicated transfectant clones (5 × 105 cells/mL) were exposed (+Dex) or not exposed (−Dex) to dexamethasone for 2 hours and then either exposed to UV irradiation for 2.5 minutes or not exposed to radiation. In experiment II, transfectants constitutively expressing mcl-1 (S3-CMVmcl-1 and S8-CMVmcl-1) and vector-only clones (V1-CMVneo and V2-CMVneo) were exposed (or not exposed) to UV irradiation for 3 minutes. Cell viability was assayed after 1 day, using the acridine orange/ethidium bromide method. The values shown are the mean ± SD of three independent experiments.

*

See Fig 1.

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