Phospholipase A2 (PLA2) activity (nmol.mg protein−1.min−1) in membrane and cytosolic subcellular fractions from human lung microvascular endothelial cells under control conditions or stimulated with thrombin (0.1 IU/ml, 5 mins) or tryptase (20 ng/ml, 5 mins). Where appropriate, cells were pretreated with bromoenol lactone (BEL, 2 µM, 10 mins) or arachidonyl trifluoromethyl ketone (AACOCF3, 5 µM, 10 mins) prior to thrombin or tryptase stimulation. PLA2 activity was measured using (16:0, [3H]18:1) plasmenylcholine substrate in the absence (4 mM EGTA) or presence (1 mM Ca2+) of calcium. Values represent mean ± SEM for separate measurements from 3 different cell isolations.