Effects of short-term in vitro exposure of SLAM SKL cells to dmPGE2 on cell cycle
In vitro treatment . | SLAM SKL cells* . | |||
---|---|---|---|---|
G0 . | G1 . | S+G2M . | % cells in cycle† . | |
Vehicle | 63.4 ± 2.5 | 2.6 ± 0.7 | 33.8 ± 2.1 | 36.4 ± 2.4 |
1 μM dmPGE2 | 54.8 ± 2.2‡ | 6.8 ± 1.9‡ | 38.4 ± 1.6‡ | 45.2 ± 2.2‡ |
In vitro treatment . | SLAM SKL cells* . | |||
---|---|---|---|---|
G0 . | G1 . | S+G2M . | % cells in cycle† . | |
Vehicle | 63.4 ± 2.5 | 2.6 ± 0.7 | 33.8 ± 2.1 | 36.4 ± 2.4 |
1 μM dmPGE2 | 54.8 ± 2.2‡ | 6.8 ± 1.9‡ | 38.4 ± 1.6‡ | 45.2 ± 2.2‡ |
Linneg cells, treated with either 1 μM dmPGE2 or vehicle for 2 hours and cultured in the presence of growth factors (50 ng/mL rmSCF, 100 ng/mL each of rhFlt-3 and rhTPO) for 20 hours, were stained with SLAM SKL, Hoechst-33342, and Pyronin-Y and the proportion of SLAM SKL cells in G0, G1, S, and G2/M phase of the cell cycle was determined by quantitation of DNA and RNA content by FACS. Data are mean plus or minus SEM for n = 9 mice, each assayed individually.
Percentage of cells in G1+S+G2M; combined data for n = 9 mice.
P < .05 compared with vehicle control.