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. 2013 Jun 10;3(2):316–333. doi: 10.3390/biom3020316

Table 2.

The effect of FTY720 vinylphosphonate on S1P formation from sphingosine in human lung endothelial cells. [32P]-labeled cells were treated with sphingosine (2 μM) for 30 min. Cells were preteated with either 10 μM (S)-FTY720 vinylphosphonate ((S)-vinylPn) or 10 μM (R)-FTY720 vinylphosphonate ((R)-vinylPn) for (A) 3 h or (B) 24 h. The [32P] S1P formed is normalized to 100,000 dpm in total lipid extracts. Results are means +/− SD for n = 3 samples.

(A) [32P] S1P formed (dpm)
Vehicle 878 +/− 6
Sphingosine 4025 +/− 47
(S)-vinylPn + Vehicle 1124 +/− 58
(S)-vinylPn + Sphingosine 5150 +/− 18
(R)-vinylPn + Vehicle 640 +/− 40
(R)-vinylPn + Sphingosine 2326 +/− 32
(B) [32P] S1P formed (dpm)
Vehicle 1015 +/− 69
Sphingosine 3665 +/− 264
(S)-vinylPn + Vehicle 1011 +/− 35
(S)-vinylPn + Sphingosine 5530 +/− 358
(R)-vinylPn + Vehicle 724 +/− 84
(R)-vinylPn + Sphingosine 2627 +/− 178