Study on Action Mode of Sphingosine 1-Phosphate in Rat Hepatocytes

Abstract

Sphingosine-1-phosphate (S1P) acts on a set of G protein-coupled receptors in the plasma membrane and also as a second messenger in certain cell types. There are two possible pathways to mobilize intracellular Ca²⁺ concentration by S1P. One is through phospholipase C, and the other is through intracellular Ca²⁺ channels operated by S1P. The Mn²⁺ quenching method was applied to elucidate the action mode of S1P-induced Ca²⁺ mobilization in rat hepatocytes. In permeabilized hepatocytes, inositol trisphosphate induced Mn²⁺ quenching, and it was blocked by heparin. However, S1P did not induce Mn²⁺ quenching. Results suggest that S1P did not mobilize Ca²⁺ through intracellular Ca²⁺ channels.