Table 2.

TPA treatment of CD34+ cells before EPO- and SCF- addition inhibits the cytokine-induced erythroid differentiation

Treatment % Positive Cells
0-24 Hours 24-144 Hours CD34 GPA CD71CD13 CD14 HLA-DR CD83 CD86 CD41
Medium EPO + SCF  9 ± 4  40 ± 5  82 ± 3 16 ± 4  3 ± 1  18 ± 4  1 ± 1  3 ± 3 7 ± 3  
TPA 100 nmol/L  EPO + SCF  25 ± 5 2 ± 1  32 ± 7  55 ± 8  6 ± 2 67 ± 5  14 ± 4  37 ± 11  20 ± 3  
TPA 10 nmol/L  EPO + SCF  17 ± 5  2 ± 1  19 ± 7 56 ± 4  4 ± 1  62 ± 11  6 ± 3 23 ± 8  21 ± 0 
Treatment % Positive Cells
0-24 Hours 24-144 Hours CD34 GPA CD71CD13 CD14 HLA-DR CD83 CD86 CD41
Medium EPO + SCF  9 ± 4  40 ± 5  82 ± 3 16 ± 4  3 ± 1  18 ± 4  1 ± 1  3 ± 3 7 ± 3  
TPA 100 nmol/L  EPO + SCF  25 ± 5 2 ± 1  32 ± 7  55 ± 8  6 ± 2 67 ± 5  14 ± 4  37 ± 11  20 ± 3  
TPA 10 nmol/L  EPO + SCF  17 ± 5  2 ± 1  19 ± 7 56 ± 4  4 ± 1  62 ± 11  6 ± 3 23 ± 8  21 ± 0 

CD34+ cells were cultured in medium alone or in the presence of 100 or 10 nmol/L TPA for 24 hours. EPO (5 U/mL) and SCF (50 ng/mL) were added, and this was followed by 6 days of incubation before staining with the indicated mAbs. Mean ± SEM of 3 to 7 experiments. GPA, glycophorin A.

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