Different response patterns of several ligands at the sphingosine-1- phosphate receptor subtype 3 (S1P 3)

Abstract

Background and purpose: Recently, some ligands targeting the sphingosine-1-phosphate receptor subtype 3 (S1P 3) have become available. The characterization of these compounds was mainly based on one functional read-out system, although S1P 3 receptors are known to activate different signal transduction pathways. Therefore, this study pharmacologically characterizes these compounds using different assays. Experimental approach: Using CHO-FlpIn cells expressing the human S1P 3 receptor the potencies and maximal effects of S1P, FTY720-P, VPC23019, VPC23153 and VPC24191 were determined in three different assays [inhibition of cAMP accumulation, elevation of intracellular calcium concentrations ([Ca 2+] i) and S1P 3 receptor internalization]. Key results: All compounds tested inhibited forskolin-induced cAMP accumulation, increased [Ca 2+] i and induced S1P 3 receptor internalization but with different potencies and maximal effects. S1P was the most potent compound in all assays followed by FTY720-P. The VPC compounds were generally less potent than S1P and FTY720-P. Regarding the maximal effects, all compounds except VPC23153, behaved as full agonists in the cAMP accumulation assay. In the calcium assay, FTY720-P, VPC23019 and VPC24191 displayed partial and VPC23153 weak partial agonist activity, relative to S1P. Interestingly, treatment with the G i inactivator Pertussis toxin, did not affect S1P-induced [Ca 2+] i elevations but inhibited those in response to the other compounds, by about 50%. Conclusions and implications: This study demonstrated differential response patterns at the S1P 3 receptor for a range of ligands. These differences could indicate the presence of functional selectivity at this receptor as FTY720-P and the VPC compounds seemed to signal predominantly via G i - whereas S1P activated G i and G q-coupled pathways. © 2009 The British Pharmacological Society.