Table 1.

The Effect of VRP on the Proliferation of HEL-JW Cells

Treatment (ng/mL)OD Value
Control 0.454 ± 0.025 
VRP (1.0) 0.458 ± 0.030 
VRP (10.0) 0.508 ± 0.029* 
VRP (100.0) 0.539 ± 0.053* 
VRP (1000.0) 0.540 ± 0.054* 
SCF (50.0) 0.632 ± 0.053 
SCF (50.0) + VRP (100.0) 0.739 ± 0.109 
IL-3 (5.0) 0.609 ± 0.041 
IL-3 (5.0) + VRP (100.0) 0.628 ± 0.096 
Treatment (ng/mL)OD Value
Control 0.454 ± 0.025 
VRP (1.0) 0.458 ± 0.030 
VRP (10.0) 0.508 ± 0.029* 
VRP (100.0) 0.539 ± 0.053* 
VRP (1000.0) 0.540 ± 0.054* 
SCF (50.0) 0.632 ± 0.053 
SCF (50.0) + VRP (100.0) 0.739 ± 0.109 
IL-3 (5.0) 0.609 ± 0.041 
IL-3 (5.0) + VRP (100.0) 0.628 ± 0.096 

HEL-JW cells (2 × 104/well) were plated in a 96-well plate, cultured with or without different concentrations of VRP in the presence or absence of SCF or IL-3 as described in Materials and Methods. After 48 hours culture, cell growth was measured by MTT assay. The OD value was obtained by measuring the absorbance at 560 nm. The results represent the mean ± SD from four similar experiments performed in triplicate.

*

Statistically significant difference (P < .01) compared with control.

Statistically significant difference (P < .05) compared with treatment by SCF (50 ng/mL) or VRP (100 ng/mL) alone.

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