Table 1

Inhibition of BFU-E and CFU-E colony formation by HZ and HNE

CFU-E
BFU-E
CFU-GM
Mean (SE)nMean (SE)nMean (SE)n
Day 4       
    HZ 59.2* (15.4) 54.6* (14.3) 76.2 (10.5) 
    HNE 51.3* (12.0) 68.2* (10.4) 84.6 (8.1) 
Day 8       
    HZ 51.4* (8.1) 51.8* (18.7) 43.2* (5.8) 
    HNE 37.3* (12.8) 53.7* (18.1) 61.8* (11.4) 
Day 14       
    HZ 35.8* (6.3) no colonies no colonies 
    HNE 45.9* (28.6) no colonies no colonies 
CFU-E
BFU-E
CFU-GM
Mean (SE)nMean (SE)nMean (SE)n
Day 4       
    HZ 59.2* (15.4) 54.6* (14.3) 76.2 (10.5) 
    HNE 51.3* (12.0) 68.2* (10.4) 84.6 (8.1) 
Day 8       
    HZ 51.4* (8.1) 51.8* (18.7) 43.2* (5.8) 
    HNE 37.3* (12.8) 53.7* (18.1) 61.8* (11.4) 
Day 14       
    HZ 35.8* (6.3) no colonies no colonies 
    HNE 45.9* (28.6) no colonies no colonies 

Growth inhibition in cultures supplemented with HZ and HNE is shown as percentage of control cell growth. Erythroid cells were cocultivated with HZ (25μM HZ-heme) or treated with HNE (7μM final concentration) or kept as untreated controls. At indicated times, 103 cells were seeded in semisolid medium to assess their colony-forming ability.

*

Significant difference (P < .05) between HZ-treated or HNE-treated cells and controls.

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