Table 1.

iNOS Activity in IL-2–Treated PB-NK Cells and S-NK

Treatment pmol Citrulline/min/mg Protein
PB-NK S-NK
+Ca/CAM −Ca/CAM + W13 +Ca/CAM −Ca/CAM + W13
Control  2.5 ± 0.9  3.0 ± 0.7  4.3 ± 0.3 5.6 ± 1.1  
IL-2  55.2 ± 3.6  57.1 ± 4.9 97.1 ± 7.7  95.3 ± 4.6  
L-NMMA  2.7 ± 0.4 2.8 ± 0.2  3.3 ± 0.8  4.8 ± 0.6  
AG 2.9 ± 0.8  2.7 ± 0.4  3.0 ± 0.9  5.7 ± 0.4 
+L-NMMA  3.0 ± 0.8  2.7 ± 0.2  5.3 ± 0.9 4.1 ± 0.6  
+AG  2.9 ± 0.1  3.1 ± 0.4 3.3 ± 0.1  3.5 ± 0.6 
Treatment pmol Citrulline/min/mg Protein
PB-NK S-NK
+Ca/CAM −Ca/CAM + W13 +Ca/CAM −Ca/CAM + W13
Control  2.5 ± 0.9  3.0 ± 0.7  4.3 ± 0.3 5.6 ± 1.1  
IL-2  55.2 ± 3.6  57.1 ± 4.9 97.1 ± 7.7  95.3 ± 4.6  
L-NMMA  2.7 ± 0.4 2.8 ± 0.2  3.3 ± 0.8  4.8 ± 0.6  
AG 2.9 ± 0.8  2.7 ± 0.4  3.0 ± 0.9  5.7 ± 0.4 
+L-NMMA  3.0 ± 0.8  2.7 ± 0.2  5.3 ± 0.9 4.1 ± 0.6  
+AG  2.9 ± 0.1  3.1 ± 0.4 3.3 ± 0.1  3.5 ± 0.6 

Isolated PB-NK or S-NK cells (106/mL) were incubated in control medium or in medium containing IL-2 (100 U/mL) for 18 hours at 37°C in 5% CO2 in air in the presence or absence of L-NMMA (500 μmol/L) or AG (50 μmol/L). Cell extracts were assayed for the enzymatic conversion of [3H]-L–arginine to [3H]-L–citrulline as described in Materials and Methods. The assay was performed in the presence or absence of CaCl2(0.6 mmol/L) and CAM (0.1 μmol/L). Data are means ± SD from one representative experiment in triplicate. Similar results were obtained in two other experiments.

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