Sphingosine 1-phosphate regulation of extracellular signal regulated kinase-1/2 in embyronic stem cells

A. Rodgers, D. Mormeneo, J.S. Long, A. Delgado, N.J. Pyne, S. Pyne

Research output: Contribution to journalArticlepeer-review

31 Citations (Scopus)

Abstract

Recent evidence suggests that sphingosine 1-phosphate (S1P) regulates self-renewal of human embryonic stem (ES) cells and differentiation of mouse embryoid bodies (derived from mouse ES cells) to cardiomyocytes. We have investigated the role of S1P in regulating ERK-1/2 signaling in mouse ES cells. In this regard, we found that both mouse ES-D3 and CGR8 cells express S1P1, S1P2, S1P3, and S1P5 but lack S1P4. The treatment of ES cells with S1P induced the activation of ERK-1/2 via a mechanism that was not mediated by S1P1, S1P2, or S1P3. This was based on: (i) the failure of S1P1, S1P2, or S1P3 antagonists to inhibit S1P-stimulated ERK-1/2 activation and (ii) the failure of SEW 2871 (S1P1 receptor agonist) to stimulate ERK-1/2 activation. The treatment of ES cells with phytosphingosine 1-phosphate (phyto-S1P), which we show here is an agonist of the S1P5 receptor, stimulated ERK-1/2 activation. These findings therefore suggest that S1P5 may mediate the effects of S1P in terms of regulating ERK-1/2 signaling in ES cells. The S1P-dependent activation of ERK-1/2 was sensitive to inhibition by pertussis toxin (uncouples the G-protein, Gi from GPCR), bisindolylmaleimide I (PKC inhibitor), and PP2 (c-Src inhibitor), but was not reduced by LY29004 (PI3K inhibitor) suggesting that S1P uses Gi-, PKC-, and c-Src-dependent mechanisms to activate the ERK-1/2 pathway in ES cells.
Original languageEnglish
Pages (from-to)1319-1330
Number of pages11
JournalStem Cells and Development
Volume18
Issue number9
DOIs
Publication statusPublished - 2009

Keywords

  • DNA
  • biosynthesis
  • embryonic stem cells
  • cytology
  • metabolism
  • gene expression
  • pharmacology

Cite this