Fig. 1.
Fig. 1. Number of CFU-Mk in the hematopoietic tissues of p45 NF-E2 mutant and control mice. Cells isolated from the fetal liver (A) or adult spleen (B and C) of wild-type (+/+), heterozygote (+/−), and p45 NF-E2 mutant homozygote (−/−) mice were cultured as described, and CFU-Mk were scored at 7 days. N = 7 and 8 for control and knockout spleens; 21 and 13 for control and knockout fetal livers, respectively. Data are presented as the number of colonies per 105 (A) or 106 cells (B) or total number of colonies per spleen (C). The modest reduction in CFU-Mk in p45 NF-E2−/− cultures shown in (A) and (B) were statistically significant, with P = .002 andP < .001, respectively; all other comparisons failed to achieve statistical significance using the Student’s t-test. In experiments for which a distinction was not made between +/+ and +/− (nonmutant) mice, these genotypes are collectively designated as +/?.

Number of CFU-Mk in the hematopoietic tissues of p45 NF-E2 mutant and control mice. Cells isolated from the fetal liver (A) or adult spleen (B and C) of wild-type (+/+), heterozygote (+/−), and p45 NF-E2 mutant homozygote (−/−) mice were cultured as described, and CFU-Mk were scored at 7 days. N = 7 and 8 for control and knockout spleens; 21 and 13 for control and knockout fetal livers, respectively. Data are presented as the number of colonies per 105 (A) or 106 cells (B) or total number of colonies per spleen (C). The modest reduction in CFU-Mk in p45 NF-E2−/− cultures shown in (A) and (B) were statistically significant, with P = .002 andP < .001, respectively; all other comparisons failed to achieve statistical significance using the Student’s t-test. In experiments for which a distinction was not made between +/+ and +/− (nonmutant) mice, these genotypes are collectively designated as +/?.

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