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. 1996 Dec 10;93(25):14586–14591. doi: 10.1073/pnas.93.25.14586

Table 3.

ICAM-1 promoter activation in UVA-irradiated 293 cells

Exposure Relative, specific luciferase activity per microgram of protein
pIC277 pIC277ΔNFkB pIC277ΔAP2
Sham 1.0  ±  0.12 1.0  ±  0.15 1.0  ±  0.18
UVA 3.0  ±  0.59 3.0  ±  0.30 1.1  ±  0.22
+ Sodium azide 1.3  ±  0.19 1.0  ±  0.10 1.3  ±  0.16
+ α-Tocopheryl succinate 1.2  ±  0.24 0.9  ±  0.18 1.1  ±  0.23
+ Deuterium oxide 3.6  ±  0.21 3.8  ±  0.15 1.0  ±  0.30

293 cells were transiently transfected with the indicated ICAM-1-based promoter constructs linked to the luciferase reporter gene, and ICAM-1 promoter activation was determined as described. Cells were either sham-irradiated or UVA-irradiated (30 J/cm2) in the presence or absence of sodium azide (50 mM) or deuterium oxide or after pretreatment with or without α-tocopheryl succinate (25 μM). Data are given as mean ± SD of relative, specific luciferase activity (per microgram of protein) and represent four experiments.