Table 3.

The CD48- subset of Thy-1lowSca-1+Lineage-c-kit+ (TSLK) cells is further enriched for long-term multilineage-reconstituting HSCs


Donor

Cell dose

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
Old     
   TSLK   5   6/9   4/9   1 in 9.0  
   TSLK   5   3/7   2/7   1 in 15.4  
   TSLK48  5   8/9   7/9   1 in 3.8  
Reconstituted     
   TSLK   10   9/11   1/11   1 in 105  
   TSLK   20   2/4   1/4   1 in 70.0  
   TSLK48  5   6/9   2/9   1 in 20.4  
Mobilized     
   TSLK   30   8/9   3/9   1 in 74.5  
   TSLK48
 
5
 
14/18
 
8/18
 
1 in 9.0
 

Donor

Cell dose

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
Old     
   TSLK   5   6/9   4/9   1 in 9.0  
   TSLK   5   3/7   2/7   1 in 15.4  
   TSLK48  5   8/9   7/9   1 in 3.8  
Reconstituted     
   TSLK   10   9/11   1/11   1 in 105  
   TSLK   20   2/4   1/4   1 in 70.0  
   TSLK48  5   6/9   2/9   1 in 20.4  
Mobilized     
   TSLK   30   8/9   3/9   1 in 74.5  
   TSLK48
 
5
 
14/18
 
8/18
 
1 in 9.0
 

The indicated number of donor-type (CD45.2+) Thy-1lowSca-1+Lineagec-kit+ cells from old bone marrow, reconstituted bone marrow, or day-7 cyclophosphanide/G-CSF–mobilized splenocytes were transplanted intravenously into lethally irradiated recipients (CD45.1+) along with 200 000 recipient-type whole bone marrow cells. The frequency of cells that gave long-term multilineage reconstitution (HSCs) was calculated based on limit-dilution (Poisson) statistics.21  Mice were considered long-term multilineage reconstituted if donor-type myeloid, B, and T cells were present for at least 16 weeks after reconstitution.

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