Table 2.

Veto Activity of C57BL/6 Sca-1+Lin Cells

Cells per Culture Stimulator and Target Origin C57BL/6 Veto CellsCTL-p Activity
% Responding CulturesInhibition (%)
40,000  C57BL/6  —  56  — 
 C57BL/6  Sca-1+Lin 0  100 
 C57BL/6  Sca-1 81  None  
 BALB/c —  80  —  
 BALB/c Sca-1+Lin 100  None 
 BALB/c  Sca-1 93  None 
10,000  C57BL/6  —  19  —  
 C57BL/6 Sca-1+Lin 0  100  
 C57BL/6 Sca-1 44  None  
 BALB/c  —  44  —  
 BALB/c  Sca-1+Lin 87  None  
 BALB/c  Sca-1 69 None 
Cells per Culture Stimulator and Target Origin C57BL/6 Veto CellsCTL-p Activity
% Responding CulturesInhibition (%)
40,000  C57BL/6  —  56  — 
 C57BL/6  Sca-1+Lin 0  100 
 C57BL/6  Sca-1 81  None  
 BALB/c —  80  —  
 BALB/c Sca-1+Lin 100  None 
 BALB/c  Sca-1 93  None 
10,000  C57BL/6  —  19  —  
 C57BL/6 Sca-1+Lin 0  100  
 C57BL/6 Sca-1 44  None  
 BALB/c  —  44  —  
 BALB/c  Sca-1+Lin 87  None  
 BALB/c  Sca-1 69 None 

Spleen cells from C3H/HeJ mice (2 × 106/mL) were incubated for 5 days with irradiated (25 Gy) allogeneic spleen cells (1 × 106/mL) from C57BL/6 (stem cell matched) or BALB/c (third-party) mice. C57BL Sca-1+Lin or Sca-1 cells were added to the primary MLC at a 0.5:1 veto:responder cell ratio. The responder cells were then recultured under limiting dilution conditions for 7 days. Cells were then harvested from individual limiting dilution culture wells and assayed for cytotoxic activity by 51Cr-release assay as described in Materials and Methods.

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