Edg-6 as a putative sphingosine 1-phosphate receptor coupling to Ca2+ signaling pathway

Citation
Y. Yamazaki et al., Edg-6 as a putative sphingosine 1-phosphate receptor coupling to Ca2+ signaling pathway, BIOC BIOP R, 268(2), 2000, pp. 583-589
Citations number
50
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
268
Issue
2
Year of publication
2000
Pages
583 - 589
Database
ISI
SICI code
0006-291X(20000216)268:2<583:EAAPS1>2.0.ZU;2-Q
Abstract
The endothelial differentiation gene-6 (Edg-6) was recently identified as a n orphan G-protein-coupled receptor. Its predicted amino acid sequence is v ery close to Edg family of receptor proteins whose ligand is supposed to be lysophosphatidic acid (LPA) or lysosphingolipid such as sphingosine 1-phos phate (S1P) and sphingosylphosphorylcholine (SPC), Transfection of the Edg- 6 into Chinese hamster ovary (CHO) cells and K562 cells resulted in the app earance of high-affinity [H-3]SIP binding activity. Among lipids employed, S1P and, even though less potent, SPC, displaced the [H-3]S1P binding, but LPA was inactive. In Edg-6-transfected CHO cells, an increase in cytosolic Ca2+ concentration in response to S1P or SPC was clearly enhanced without c hange in the LPA-induced action as compared with the vector-transfected cel ls. The enhancement of the Ca2+ response was associated with a significant accumulation of inositol phosphate, reflecting activation of phospholipase C. Similar enhancement of Ca2+ response to S1P or SPC was also observed in Edg-6-expressing K562 cells. These lipid-induced actions in CHO cells and K 562 cells expressing Edg-6 were markedly suppressed by pertussis toxin trea tment. We conclude that Edg-6 is one of S1P or lysosphingolipid receptors t hat couple to phospholipase C-Ca2+ system through pertussis toxin-sensitive G-proteins, 2000 Academic Press.