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. Author manuscript; available in PMC: 2013 Dec 1.
Published in final edited form as: J Neuroimmune Pharmacol. 2012 Aug 1;7(4):969–980. doi: 10.1007/s11481-012-9390-z

Fig. 7.

Fig. 7

GRE luciferase reporter activity in HEK293T cells treated with Δ9-THC and/or DEX. HEK293T cells (5×106 cells) were preseeded in a 6 well plate in growth medium overnight. The cells were then transiently transfected with pGRE-luc or pTAL-luc (vector control plasmid). After transfection, cells were treated with 0.1 % EtOH (VH), 0.5 μM DEX, different concentration of Δ9-THC (1, 5, and 10 μM), or the combination of 0.5 μM DEX plus 10 μM Δ9-THC. 24 h after transfection, luciferase activity was quantified in CPS and normalized to total protein (μg). The results are the mean±SEM. The “ns” indicates no significant difference. Results are representative of two separate experiments with three replicates per treatment group