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. 1998 Jun 9;95(12):7006–7011. doi: 10.1073/pnas.95.12.7006

Table 1.

Differentiation of primary hematopoietic precursor cells

Exp. Virus EPO antiserum No. CFU-E No. CFU-E (−uninfected control) No. BFU-E No. BFU-E (−uninfected control)
A Uninfected 5  ±  1 0 5  ±  2 0
+ 0 0 0 0
Uninfected + EPO 71  ±  10 66 8  ±  3 3
+ 7  ±  4 7 2  ±  1 2
cEPOR 141  ±  23 136 42  ±  2 37
+ 79  ±  11 79 30  ±  7 30
cEPOR (1–255) 20  ±  8 15 15  ±  3 10
+ 9  ±  2 9 2  ±  2 2
cEPOR/G-CSFR 97  ±  9 92 17  ±  3 12
+ 76  ±  22 76 9  ±  1 9
cEPOR/GHR 79  ±  6 74 13  ±  2 8
+ 63  ±  12 63 8  ±  2 8
B Uninfected 4  ±  2 0 9  ±  6 0
+ 0 0 2  ±  1 0
cEPOR 67  ±  12 63 28  ±  5 19
+ 39  ±  9 39 12  ±  3 10
cEPOR/Mpl 33  ±  10 29 8  ±  2 0
+ 5  ±  2 5 1  ±  0.4 0

Embryonic day 13 fetal liver cells were prepared and infected. To each dish, either normal rabbit IgG (0.5 μg/ml) or rabbit polyclonal antierythropoietin antibody (+, 5 μg/ml) were added. In one condition (+EPO) human EPO was added to the cultures at 0.3 unit/ml. CFU-E numbers were determined at day 2 of culture; BFU-E numbers were determined at day 7. Data are expressed as mean ± SD (n = 4). Experiments A and B were performed on separate days.