Table 5.

CD150+CD48-Sca-1+Lineage-c-kit+ cells from old, reconstituted, and cyclophosphamide/G-CSF-mobilized mice are highly enriched for long-term self-renewing, multipotent HSCs


Donor/experiment

No. mice that engrafted/no. mice total

No. mice with long-term multilineage reconstitution/no. mice total

Frequency of cells that long-term multilineage reconstituted
Young    
   1   8/8   7/8   1 in 2.0  
Old    
   1   4/7   3/7   1 in 5.9  
   2   6/12   5/12   1 in 6.1  
   3   5/9   3/9   1 in 7.9  
   4   4/9   3/9   1 in 7.9  
Reconstituted    
   1   3/6   3/6   1 in 4.8  
   2   12/13   10/13   1 in 2.6  
   3   7/9   3/9   1 in 7.9  
Mobilized    
   1
 
5/8
 
5/8
 
1 in 3.6
 

Donor/experiment

No. mice that engrafted/no. mice total

No. mice with long-term multilineage reconstitution/no. mice total

Frequency of cells that long-term multilineage reconstituted
Young    
   1   8/8   7/8   1 in 2.0  
Old    
   1   4/7   3/7   1 in 5.9  
   2   6/12   5/12   1 in 6.1  
   3   5/9   3/9   1 in 7.9  
   4   4/9   3/9   1 in 7.9  
Reconstituted    
   1   3/6   3/6   1 in 4.8  
   2   12/13   10/13   1 in 2.6  
   3   7/9   3/9   1 in 7.9  
Mobilized    
   1
 
5/8
 
5/8
 
1 in 3.6
 

Three (CD45.1+) CD50+CD48Sca-1+linc-kit+ cells from old, reconstituted, or day-7 cyclophosphamide/G-CSF–mobilized splenocytes were transplanted intravenously into lethally irradiated recipients (CD45.2+) along with 300 000 CD150 recipient-type cells or 200 000 whole bone marrow cells for radioprotection. There was no apparent difference in the frequency of donor cells that long-term multilineage reconstituted based on the nature of cells used for radioprotection. Recipients were considered long-term multilineage reconstituted if donor-type myeloid, B, and T cells were present for at least 16 weeks after transplantation.

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