Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-178 |
Sentence |
denotes |
Localization of endothelial nitric-oxide synthase phosphorylated on serine 1179 and nitric oxide in Golgi and plasma membrane defines the existence of two pools of active enzyme. |
T1 |
0-178 |
Sentence |
denotes |
Localization of endothelial nitric-oxide synthase phosphorylated on serine 1179 and nitric oxide in Golgi and plasma membrane defines the existence of two pools of active enzyme. |
TextSentencer_T2 |
179-341 |
Sentence |
denotes |
The subcellular localization of endothelial nitric-oxide synthase (eNOS) is critical for optimal coupling of extracellular stimulation to nitric oxide production. |
T2 |
179-341 |
Sentence |
denotes |
The subcellular localization of endothelial nitric-oxide synthase (eNOS) is critical for optimal coupling of extracellular stimulation to nitric oxide production. |
TextSentencer_T3 |
342-545 |
Sentence |
denotes |
Because eNOS is activated by Akt-dependent phosphorylation to produce nitric oxide (NO), we determined the subcellular distribution of eNOS phosphorylated on serine 1179 using a variety of methodologies. |
T3 |
342-545 |
Sentence |
denotes |
Because eNOS is activated by Akt-dependent phosphorylation to produce nitric oxide (NO), we determined the subcellular distribution of eNOS phosphorylated on serine 1179 using a variety of methodologies. |
TextSentencer_T4 |
546-690 |
Sentence |
denotes |
Based on sucrose gradient fractionation, phosphorylated-eNOS (P-eNOS) was found in both caveolin-1-enriched membranes and intracellular domains. |
T4 |
546-690 |
Sentence |
denotes |
Based on sucrose gradient fractionation, phosphorylated-eNOS (P-eNOS) was found in both caveolin-1-enriched membranes and intracellular domains. |
TextSentencer_T5 |
691-933 |
Sentence |
denotes |
Co-transfection of eNOS with Akt and stimulation of endothelial cells with vascular endothelial growth factor (VEGF) increased the ratio of P-eNOS to total eNOS but did not change the relative intracellular distribution between these domains. |
T5 |
691-933 |
Sentence |
denotes |
Co-transfection of eNOS with Akt and stimulation of endothelial cells with vascular endothelial growth factor (VEGF) increased the ratio of P-eNOS to total eNOS but did not change the relative intracellular distribution between these domains. |
TextSentencer_T6 |
934-1176 |
Sentence |
denotes |
The proper localization of eNOS to intracellular membranes was required for agonist-dependent phosphorylation on serine 1179, since VEGF did not increase eNOS phosphorylation in cells transfected with a non-acylated, mistargeted form of eNOS. |
T6 |
934-1176 |
Sentence |
denotes |
The proper localization of eNOS to intracellular membranes was required for agonist-dependent phosphorylation on serine 1179, since VEGF did not increase eNOS phosphorylation in cells transfected with a non-acylated, mistargeted form of eNOS. |
TextSentencer_T7 |
1177-1340 |
Sentence |
denotes |
Confocal imaging of P-eNOS and total eNOS pools demonstrated co-localization in the Golgi region and plasmalemma of transfected cells and native endothelial cells. |
T7 |
1177-1340 |
Sentence |
denotes |
Confocal imaging of P-eNOS and total eNOS pools demonstrated co-localization in the Golgi region and plasmalemma of transfected cells and native endothelial cells. |
TextSentencer_T8 |
1341-1475 |
Sentence |
denotes |
Finally, VEGF stimulated a large increase in NO localized in both the perinuclear region and the plasma membrane of endothelial cells. |
T8 |
1341-1475 |
Sentence |
denotes |
Finally, VEGF stimulated a large increase in NO localized in both the perinuclear region and the plasma membrane of endothelial cells. |
TextSentencer_T9 |
1476-1598 |
Sentence |
denotes |
Thus, activated, phosphorylated eNOS resides in two cellular compartments and both pools are VEGF-regulated to produce NO. |
T9 |
1476-1598 |
Sentence |
denotes |
Thus, activated, phosphorylated eNOS resides in two cellular compartments and both pools are VEGF-regulated to produce NO. |