Journal of Pharmacological Sciences (Jan 2005)

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

  • Young-Jin Im,
  • Dong-Soon Im,
  • Yun-Kyung Lee,
  • Eun-Hee Lee,
  • Koichi Sato,
  • Hideaki Tomura,
  • Toshiaki Katada,
  • Michio Ui,
  • Fumikazu Okajima

Journal volume & issue
Vol. 97, no. 3
pp. 443 – 446

Abstract

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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. Keywords:: hepatocyte, sphingosine 1-phosphate, second messenger