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Articles

Inhibition of ATP-synthase potentiates cytotoxicity of combination drug menadione/ascorbate in leukaemia lymphocytes

, , , , , & ORCID Icon show all
Pages 1738-1744 | Received 25 Jun 2021, Accepted 17 Oct 2021, Published online: 21 Jan 2022

Figures & data

Figure 1. Effect of oligomycin-A (100 ng/mL) on the cell viability and proliferation of M/A-treated leukaemic lymphocytes (Jurkat) after 24 h and 48 h of incubation in humidified atmosphere. Data are means ± SD from three independent experiments with two parallel measurements for each experiment. *p < 0.05, **p < 0.01: oligomycin/M/A-treated versus the respective M/A-treated cells or oligomycin-treated sample versus the untreated cells (control). Red dashed line indicates the initial cell number in the suspension.

Figure 1. Effect of oligomycin-A (100 ng/mL) on the cell viability and proliferation of M/A-treated leukaemic lymphocytes (Jurkat) after 24 h and 48 h of incubation in humidified atmosphere. Data are means ± SD from three independent experiments with two parallel measurements for each experiment. *p < 0.05, **p < 0.01: oligomycin/M/A-treated versus the respective M/A-treated cells or oligomycin-treated sample versus the untreated cells (control). Red dashed line indicates the initial cell number in the suspension.

Figure 2. Effect of oligomycin-A (100 ng/mL) on the absolute steady-state ATP levels in M/A-treated leukaemic lymphocytes (Jurkat) after 24 h and 48 h of incubation in humidified atmosphere. Data are means ± SD from three independent experiments with four parallel measurements for each experiment. *p < 0.05, **p < 0.01, p < 0.001: oligomycin/M/A-treated versus the respective M/A-treated cells or oligomycin-treated sample versus the untreated cells (control). ATP-based luminescence in the untreated cells was considered 100%.

Figure 2. Effect of oligomycin-A (100 ng/mL) on the absolute steady-state ATP levels in M/A-treated leukaemic lymphocytes (Jurkat) after 24 h and 48 h of incubation in humidified atmosphere. Data are means ± SD from three independent experiments with four parallel measurements for each experiment. *p < 0.05, **p < 0.01, p < 0.001: oligomycin/M/A-treated versus the respective M/A-treated cells or oligomycin-treated sample versus the untreated cells (control). ATP-based luminescence in the untreated cells was considered 100%.

Figure 3. Effect of oligomycin-A (100 ng/mL) on the normalized steady-state ATP levels in M/A-treated leukaemic lymphocytes (Jurkat) after 24 h and 48 h of incubation in humidified atmosphere. Data are means ± SD from three independent experiments with four parallel measurements for each experiment. *p < 0.05, **p < 0.01, ***p < 0.001: oligomycin/M/A-treated versus the respective M/A-treated cells or oligomycin-treated sample versus the untreated cells (control). Data were normalized to an equal number of live cells in each sample (1 × 106 cells), as only living cells synthesize ATP. Normalized ATP-based luminescence in the untreated cells was considered 100%.

Figure 3. Effect of oligomycin-A (100 ng/mL) on the normalized steady-state ATP levels in M/A-treated leukaemic lymphocytes (Jurkat) after 24 h and 48 h of incubation in humidified atmosphere. Data are means ± SD from three independent experiments with four parallel measurements for each experiment. *p < 0.05, **p < 0.01, ***p < 0.001: oligomycin/M/A-treated versus the respective M/A-treated cells or oligomycin-treated sample versus the untreated cells (control). Data were normalized to an equal number of live cells in each sample (1 × 106 cells), as only living cells synthesize ATP. Normalized ATP-based luminescence in the untreated cells was considered 100%.

Figure 4. Effect of oligomycin-A (100 ng/mL) on the mitochondrial superoxide of M/A-treated leukaemic lymphocytes (Jurkat) after 24 h and 48 h of incubation in humidified atmosphere. Data are means ± SD from three independent experiments with two parallel measurements for each experiment. *p < 0.05, **p < 0.01: oligomycin/M/A-treated versus the respective M/A-treated cells or oligomycin-treated sample versus the untreated cells (control).

Figure 4. Effect of oligomycin-A (100 ng/mL) on the mitochondrial superoxide of M/A-treated leukaemic lymphocytes (Jurkat) after 24 h and 48 h of incubation in humidified atmosphere. Data are means ± SD from three independent experiments with two parallel measurements for each experiment. *p < 0.05, **p < 0.01: oligomycin/M/A-treated versus the respective M/A-treated cells or oligomycin-treated sample versus the untreated cells (control).

Data availability statement

The data that support the findings of this study are available on request from the corresponding authors (ZZ and BN).