Table 1.

Characteristics of hematopoietic cell populations

Cell Population HPP-CFC per 1000 Lymphohematopoietic Potential
Normal bone marrow (NBM) 0.50 ± 0.06  ND  
NBM Lin(−)  97 ± 10  
NBM Lin(−)Sca-1(−)c-kit(+)  96 ± 7  −  
NBM Lin(−)Sca-1(+)c-kit(+)  415 ± 6  +  
2-day 5 FU BM Lin(−)Sca-1(+)c-kit(+)  194 ± 30  +  
NBM Lin(−)Sca-1(+)c-kit(+)CD34(+)  15 ± 7  ND  
NBM Lin(−)Sca-1(+)c-kit(+)CD34(−)  191 ± 64  ND 
Cell Population HPP-CFC per 1000 Lymphohematopoietic Potential
Normal bone marrow (NBM) 0.50 ± 0.06  ND  
NBM Lin(−)  97 ± 10  
NBM Lin(−)Sca-1(−)c-kit(+)  96 ± 7  −  
NBM Lin(−)Sca-1(+)c-kit(+)  415 ± 6  +  
2-day 5 FU BM Lin(−)Sca-1(+)c-kit(+)  194 ± 30  +  
NBM Lin(−)Sca-1(+)c-kit(+)CD34(+)  15 ± 7  ND  
NBM Lin(−)Sca-1(+)c-kit(+)CD34(−)  191 ± 64  ND 

ND, not determined.

Hematopoietic progenitor cells were isolated from NBM or from 2d 5FU-treated BM of C57BL/6 mice as described in “Materials and Methods.” Sorted subpopulations were tested in various assays to establish their positions in the stem/progenitor cell differentiation pathway: HPP-CFC was assayed by incubating 100 to 500 cells in methylcellulose medium containing rmSF (50 ng/mL), rmIL-3 (20 ng/mL), rhIL-11 (50 ng/nL), and rhEPO (2 U/mL) for 14 days and by counting colonies with diameters greater than 2 mm. Lymphohematopoietic potential was defined as the ability of primary colonies grown for 8 to 12 days in SF + IL-11 to produce secondary colonies containing B220+ pre-B cells in rmSF + IL-7 supplemented methylcellulose cultures on replating. All results are expressed as mean ± SEM from 3 to 4 experiments.

Close Modal

or Create an Account

Close Modal
Close Modal