Journal of Investigative Medicine | VOL. 54


Publication Date Mar 1, 2006


Rationale Modulation of pulmonary vascular barrier function is an important clinical goal given the devastating effects of vascular leak in ARDS. We and others have demonstrated that FTY720, an analog of the potent barrier-enhancing phospholipid sphingosine 1-phosphate (S1P), is also barrier protective through incompletely characterized mechanisms. We utilized various FTY analogs to better define FTY effects on endothelial cell (EC) barrier function. 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) but with a delayed onset and slower rate of TER rise relative to S1P (1 μM). Previous siRNA experiments have suggested that FTY does not exert its barrier-enhancing effects through the same S1P1R receptor required for S1P. We now report that FTY also increases TER in EC derived from embryonic S1P1R -/- mice, providing further support for a novel FTY barrier-enhancing pathway. In addition, S1P3R is not the responsible receptor as S1P3R siRNA did not alter FTY-induced TER increases. Increasing concentrations of phosphorylated FTY (0.1-50 μM) produced a faster TER elevation rate of onset than FTY itself but never reached the rate of rise observed with S1P. (R)-phosphonate and enephosphonate analogs of FTY (1-50 μM) produced rapid TER elevations similar to S1P, while the (S)-analogs were less potent or even barrier-disruptive. Both (R)- and (S)-regioisomers of FTY were barrier disruptive. Conclusion T...


Transendothelial Electrical Resistance Sphingosine 1-phosphate Endothelial Cell Barrier Function Barrier Enhancing Effects Pulmonary Barrier Function Endothelial Cell Endothelial Cell Barrier Barrier Function Pulmonary Barrier Pulmonary Endothelial Cell Barrier

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