Journal of Investigative Medicine | VOL. 53


Publication Date Mar 1, 2005


Rationale Disruption of pulmonary vascular integrity occurs during inflammatory disease processes such as acute lung injury and sepsis, and as a result, regulation of this barrier is an important clinical objective. We have described rapid endothelial cell (EC) barrier enhancement by the platelet-derived phospholipid, sphingosine 1-phosphate (S1P), mediated via S1P1 receptor (S1P1R) ligation. FTY720, an immunosuppressive drug currently in phase III clinical trials, is phosphorylated in vivo to form a structural analogue of S1P. We and others have demonstrated that FTY720 also induces EC barrier enhancement, and we now explore the role of S1P1R ligation in this process. Methods/Results FTY (1 μM) significantly increased cultured human pulmonary artery EC barrier function in a sustained manner as measured by transendothelial electrical resistance (TER), with a delayed onset and slower rate of rise relative to S1P (1 μM). Lipid extraction and 2-phase thin layer chromatography studies revealed that phosphorylation of FTY is not required for barrier enhancement. Both S1P- and FTY-induced barrier enhancement were abolished by pretreatment with pertussis toxin; however, reduction of S1P1R expression via siRNA significantly inhibited S1P-, but not FTY-induced TER elevation. Both S1P and FTY rapidly (within 5 min) induced S1P1R accumulation in membrane lipid rafts, but only S1P stimulated threonine phosphorylation of S1P1R. Inhibition of this phosphorylation by preincubation with the PI3 kinase inhibitor LY294002 (10 μM) blocked S1P-...


Sphingosine 1-phosphate Endothelial Cell Barrier Transendothelial Electrical Resistance S1P1 Receptor Barrier Enhancement Endothelial Cell Barrier Enhancement PI3 Kinase Inhibitor LY294002 Endothelial Cell Barrier Function Endothelial Cell Membrane Lipid Rafts

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