Fig. 5.
Fig. 5. Functional characterization of steady-state BM CD34+ cells isolated in subcompartments of G0 /G1 phase. (A) Progenitor cell assay. The number of hematopoietic colonies are given per 100 cells plated. Data shown above are the mean ± SEM of three experiments performed in duplicate. BFU-E, burst-forming unit–erythroid; CFU-GM, colony-forming unit–granulocyte/macrophage; CFU-MIX, CFU-mixed. *P < .05 v G1a , G1b , and G1c CD34+ cells; **P < .05 v G1a and G1b CD34+ cells. (B) LTHC-IC assay. Frequencies are given per 100 cells as the mean ± SEM, n = 4. ***P < .05 v G1b and G1c CD34+ cells. Statistical analysis was made by ANOVA followed by SNK pairwise comparisons.

Functional characterization of steady-state BM CD34+ cells isolated in subcompartments of G0 /G1 phase. (A) Progenitor cell assay. The number of hematopoietic colonies are given per 100 cells plated. Data shown above are the mean ± SEM of three experiments performed in duplicate. BFU-E, burst-forming unit–erythroid; CFU-GM, colony-forming unit–granulocyte/macrophage; CFU-MIX, CFU-mixed. *P < .05 v G1a , G1b , and G1c CD34+ cells; **P < .05 v G1a and G1b CD34+ cells. (B) LTHC-IC assay. Frequencies are given per 100 cells as the mean ± SEM, n = 4. ***P < .05 v G1b and G1c CD34+ cells. Statistical analysis was made by ANOVA followed by SNK pairwise comparisons.

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