Figure 1: General structure of 3-amino-7-benzylbenzimidazo[3,2- a]quinolinium chloride (ABQ-48: NSC D-763307) and 3-nitro- 7-benzylbenzimidazo[3,2-a]quinolinium chloride (NBQ-48: NSC D -763303)
|
ABQ-48, μg/mL |
Cytokine |
Cytokine concentration, pg/mL±SEM |
|
0.6 |
G-CSF |
32.3±22.8 |
|
0.3 |
IL-2 |
18.5±7.2 |
|
1.2 |
IL-6 |
61.9±20.4 |
|
5.0 |
IFN- |
21.7±12.8 |
Table 1: : Maximal concentrations of cytokines produced in culture supernatants from ABQ-48-treated lymphocyte cultures. Murine splenic lymphocytes were isolated and incubated with twofold serial dilutions of ABQ-48 (5-0.3 µg/mL) for 5 days. Culture supernatants were collected and the cytokine concentrations were determined by protein microarray analysis. Supernatants from Concanavalin A-treated lymphocytes, and media alone were used as positive and negative controls, respectively. Results were expressed as mean concentrations SEM of three independent experiments.
|
NBQ-48, μg/mL |
Cytokine |
Cytokine concentration, pg/mL±SEM |
|
0.6 |
G-CSF |
67.6±57.5 |
|
2.5 |
IL-2 |
37.2±15.1 |
|
5.0 |
IL-6 |
65.2±40.2 |
|
0.6 |
IFN- |
3.8±3.8 |
Table 2: : Maximal concentrations of cytokines produced in culture supernatants from NBQ-48-treated lymphocyte cultures. Murine splenic lymphocytes were isolated and incubated with twofold serial dilutions of NBQ-48 (5-0.3 μg/mL) for 5 days. Culture supernatants were collected and the cytokine concentrations were determined by protein microarray analysis. Supernatants from Concanavalin A-treated lymphocytes, and media alone were used as positive and negative controls, respectively. Results were expressed as mean concentrations ± SEM of three independent experiments.
Figure 1: General structure of 3-amino-7-benzylbenzimidazo[3,2- a]quinolinium chloride (ABQ-48: NSC D-763307) and 3-nitro- 7-benzylbenzimidazo[3,2-a]quinolinium chloride (NBQ-48: NSC D -763303)
Figure 2: Production of G-CSF, IL-2, IL-6, and IFN-γ in culture supernatants from ABQ 48-treated lymphocyte cultures. Murine splenic lymphocytes were isolated and incubated with twofold serial dilutions of ABQ-48 (5-0.3 ug/mL) for 5 days. Culture supernatants were collected and the cytokine concentrations were determined by protein microarray analysis. Supernatants from Concanavalin A-treated lymphocytes, and media alone were used as positive and negative controls, respectively. Results were expressed as mean concentrations ± SEM of three independent experiments.
Figure 3: Production of G-CSF, IL-2, IL-6, and IFN-γ in culture supernatants from NBQ 48-treated lymphocyte cultures. Murine splenic lymphocytes were isolated and incubated with twofold serial dilutions of NBQ-48 (5-0.3 μg/mL) for 5 days. Culture supernatants were collected and the cytokine concentrations were determined by protein microarray analysis. Supernatants from Concanavalin A-treated lymphocytes, and media alone were used as positive and negative controls, respectively. Results were expressed as mean concentrations ± SEM of three independent experiments.
Tables at a glance
Figures at a glance