Fig. 5.
Fig. 5. Effect of rhTNF-α on apoptotic depletion of normal BM erythroid cells. / We incubated 1 × 106 BM cells from healthy subjects (n = 3) in the absence or presence of human rhTNF-α at concentrations of 10 ng/mL and 20 ng/mL for 48 hours. The percentage of apoptotic cells in the early progenitor (⋄) CD34+/CD71+, the early precursor (■) CD36+/glycoA+, and late precursor (○) CD36−/glycoA+ cell compartments were evaluated using flow cytometry and 7AAD. Each point in the diagram represents the mean (± SEM) of the 3 experiments. Comparison between treated and untreated with rhTNF-α cultures in each cell compartment was performed using the ANOVA test.

Effect of rhTNF-α on apoptotic depletion of normal BM erythroid cells.

We incubated 1 × 106 BM cells from healthy subjects (n = 3) in the absence or presence of human rhTNF-α at concentrations of 10 ng/mL and 20 ng/mL for 48 hours. The percentage of apoptotic cells in the early progenitor (⋄) CD34+/CD71+, the early precursor (■) CD36+/glycoA+, and late precursor (○) CD36/glycoA+ cell compartments were evaluated using flow cytometry and 7AAD. Each point in the diagram represents the mean (± SEM) of the 3 experiments. Comparison between treated and untreated with rhTNF-α cultures in each cell compartment was performed using the ANOVA test.

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