Table 1.

MRA of HSC Subsets Isolated by Fluorescent Staining With Rh-123, JC-1, or NAO

Cells Transplanted Cells/Femur Low/High RatioCFU-S/Femur Low/High Ratio
Experiment No. 1  
 None 3.1 × 105  4.7 ± 1.1 
 Rh-123low 5.3 × 106  115 ± 78-150 
 Rh-123high 2.2 × 106 2.41  4.4 ± 2.4  26.1 
 JC-1low 1.6 × 107  206 ± 66  
 JC-1high 2.8 × 106 5.71  0.6 ± 1.3  343 
Experiment No. 2  
 None  4.7 × 105  3.4 ± 0.3  
 Rh-123low 1.3 × 107  425 ± 202 
 Rh-123high 3.3 × 106 3.94 3.8 ± 2.5  112  
 NAOlow 4.6 × 106  49 ± 8.5 
 NAOhigh 4.8 × 106 0.96 75 ± 18-151 0.65 
Cells Transplanted Cells/Femur Low/High RatioCFU-S/Femur Low/High Ratio
Experiment No. 1  
 None 3.1 × 105  4.7 ± 1.1 
 Rh-123low 5.3 × 106  115 ± 78-150 
 Rh-123high 2.2 × 106 2.41  4.4 ± 2.4  26.1 
 JC-1low 1.6 × 107  206 ± 66  
 JC-1high 2.8 × 106 5.71  0.6 ± 1.3  343 
Experiment No. 2  
 None  4.7 × 105  3.4 ± 0.3  
 Rh-123low 1.3 × 107  425 ± 202 
 Rh-123high 3.3 × 106 3.94 3.8 ± 2.5  112  
 NAOlow 4.6 × 106  49 ± 8.5 
 NAOhigh 4.8 × 106 0.96 75 ± 18-151 0.65 

Mouse HSC isolated by the Thy-1.1lowSca-1+Lin phenotype were further separated based on levels of JC-1, NAO, or Rh-123 staining. Cells in the upper 30% and lower 30% of staining intensity were isolated in each case, and approximately 2,000 cells of each population were transplanted into two lethally irradiated syngeneic mice. Twelve to 13 days later the cellularity of the femurs was determined; the numbers indicate the cell count derived from four pooled femurs. CFU-S/femur indicates the content of day 13 CFU-S per femur in the primary transplant recipients (mean ± SD), as measured in groups of four secondary recipient mice except as noted.

F0-150

Eight secondary recipients analyzed.

F0-151

Three secondary recipients analyzed.

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