Skip to main content
. 2018 Sep 24;7(1):13–24.

TABLE 1.

GLUCOCORTICOIDS RESPONSIVENESS OF THE Nat2*-HRE TRANSFECTED INTO CV1 CELLS

CAT Constructs rGR Butylated Chloramphenicol (× 104 dpm) ± SEM
Hormone Treatment
No Hormone Dexamethasone DHT β-Estradiol
0 × HRE + 0.63 ± 0.03 0.31 ± 0.08 0.52 ± 0.08 0.78 ± 0.07
1 × HRE + 8.70 ± 0.44 4.21 ± 0.30 nd nd
2 × HRE 6.42 ± 0.42 8.52 ± 0.76 nd nd
2 × HRE + 3.86 ± 0.58 41.37 ± 2.94 3.98 ± 0.16 5.06 ± 0.51
3 × HRE3 + 9.41 ± 0.63 111.00 ± 5.27 nd nd

Cells were cotransfected with 100 ng of rat glucocorticoid receptor (GR) and 2 μg of target DNA (0 × HRE, 1 × HRE, 2 × HRE, or 3 × HRE3). Subsequent treatment was for 72 h with no hormone, 340 nM DHT, 100 nM dexamethasone, or 100 nM β-estradiol. Cells were also transfected in the presence or absence of GR. CAT activities measured as the formation of butylated chloramphenicol were normalized to total amount of protein (mg) and are expressed as average (× 104 dpm) of triplicate samples ± SEM. nd, not determined.