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. 1998 Jan;18(1):499–511. doi: 10.1128/mcb.18.1.499

TABLE 2.

Differentiation profiles of 32D cells overexpressing chimeric genes between c-myb and B-myba

Cell line Days after GCSF addition % of following cell type (mean ± SD)
Myeloblast Promyelocyte/myelocyte Metamyelocyte/granulocyte
32D/PMT-Neo (−Zn) 0 97.7 ± 1.5 2.3 ± 1.5
4 7.0 ± 1 85.7 ± 1.5 7.3 ± 0.6
7 0.3 ± 0.6 76.0 ± 4.6 23.3 ± 2.5
32D/PMT-Neo (+Zn) 0 98.3 ± 0.6 1.7 ± 0.6
4 12.0 ± 3 77.7 ± 6.8 10.3 ± 4
7 0.7 ± 0.6 80.3 ± 2.5 19.0 ± 2.6
Chimera CBC (−Zn) 0 99.0 ± 1 1.0 ± 1
4 3.7 ± 1.2 85.0 ± 3.6 11.3 ± 2.5
7 0.7 ± 1.1 77.7 ± 4.6 21.3 ± 3.8
Chimera CBC (+Zn) 0 97.7 ± 1.5 2.3 ± 1.5
4 2.7 ± 2 84.0 ± 1 13.3 ± 2.3
7 74.0 ± 7.8 26.0 ± 6.5
Chimera CCB (−Zn) 0 98.0 ± 1 2.0 ± 1
4 47.3 ± 2.5 52.7 ± 2.9
7 2.7 ± 2.5 97.3 ± 8.7
Chimera CCB (+Zn) 0 97 ± 1 3.0 ± 1
4 44.0 ± 3.6 56.0 ± 6
7 2.7 ± 2.5 97.3 ± 7.5
Chimera CBB (−Zn) 0 97 ± 1 3.0 ± 1
4 34.7 ± 2.5 65.3 ± 4.9
7 1.0 ± 1 99.0 ± 3.4
Chimera CBB (+Zn) 0 97.7 ± 1.5 2.3 ± 1.5
4 10.3 ± 2.3 89.7 ± 6.5
7 3.0 ± 1 97.0 ± 3.6
a

32D cells overexpressing each transgene were induced to differentiate by G-CSF. On the indicated days, aliquots of the cells were cytospun and stained with May-Grunwald-Giemsa. The values are means from three studies ± standard deviations. 

b

−Zn, lacking zinc; +Zn, with zinc.