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. Author manuscript; available in PMC: 2010 Mar 25.
Published in final edited form as: Respir Physiol Neurobiol. 2008 Nov 18;165(2-3):167–174. doi: 10.1016/j.resp.2008.11.006

Table No. 1.

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.

Cell Fraction EGTA Ca2+ EGTA Ca2+ EGTA Ca2+
BEL BEL AACOCF3 AACOCF3
Membrane Control 4.22 ± 0.16 4.56 ± 0.21 1.81 ± 0.12 1.72 ± 0.21 4.19 ± 0.21 4.33 ± 0.31
Thrombin 8.78 ± 0.34 9.13 ± 0.57 3.11 ± 0.31 2.95 ± 0.37 7.94 ± 0.52 8.03 ± 0.41
Tryptase 8.19 ± 0.48 8.56 ± 0.41 2.78 ± 0.42 2.56 ± 0.18 8.31 ± 0.47 8.55 ± 0.18
Cytosol Control 0.42 ± 0.05 0.51 ± 0.06 0.19 ± 0.04 0.21 ± 0.04 0.29 ± 0.05 0.31 ± 0.08
Thrombin 0.48 ± 0.12 0.51 ± 0.12 0.22 ± 0.02 0.16 ± 0.03 0.32 ± 0.04 0.31 ± 0.09
Tryptase 0.45 ± 0.09 0.53 ± 0.12 0.17 ± 0.02 0.23 ± 0.02 0.29 ± 0.03 0.27 ± 0.05