2. Academic Validation
  3. Sphingosine 1-phosphate (S1P) suppresses the collagen-induced activation of human platelets via S1P4 receptor

Sphingosine 1-phosphate (S1P) suppresses the collagen-induced activation of human platelets via S1P4 receptor

  • Thromb Res. 2017 Aug;156:91-100. doi: 10.1016/j.thromres.2017.06.001.
Takashi Onuma 1,  Kumiko Tanabe 2,  Yuko Kito 1,  Masanori Tsujimoto 3,  Kodai Uematsu 3,  Yukiko Enomoto 4,  Rie Matsushima-Nishiwaki 5,  Tomoaki Doi 6,  Kiyoshi Nagase 2,  Shigeru Akamatsu 7,  Haruhiko Tokuda 8,  Shinji Ogura 6,  Toru Iwama 4,  Osamu Kozawa 9,  Hiroki Iida 2
Affiliations

Affiliations

  • 1 Department of Anesthesiology and Pain Medicine, Gifu University Graduate School of Medicine, Gifu, Japan; Department of Pharmacology, Gifu University Graduate School of Medicine, Gifu, Japan.
  • 2 Department of Anesthesiology and Pain Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • 3 Department of Pharmacology, Gifu University Graduate School of Medicine, Gifu, Japan; Department of Neurosurgery, Gifu University Graduate School of Medicine, Gifu, Japan.
  • 4 Department of Neurosurgery, Gifu University Graduate School of Medicine, Gifu, Japan.
  • 5 Department of Pharmacology, Gifu University Graduate School of Medicine, Gifu, Japan.
  • 6 Department of Emergency and Disaster Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
  • 7 Department of Anesthesiology and Critical Care Medicine, Chuno Kosei Hospital, Seki, Japan.
  • 8 Department of Clinical Laboratory and Biobank, National Center for Geriatrics and Gerontology, Obu, Japan.
  • 9 Department of Pharmacology, Gifu University Graduate School of Medicine, Gifu, Japan. Electronic address: okozawa@gifu-u.ac.jp.
PMID: 28609704 DOI: 10.1016/j.thromres.2017.06.001
Abstract

Sphingosine 1-phosphate (S1P) is as an extracellular factor that acts as a potent lipid mediator by binding to specific receptors, S1P receptors (S1PRs). However, the precise role of S1P in human platelets that express S1PRs has not yet been fully clarified. We previously reported that heat shock protein 27 (HSP27) is released from human platelets accompanied by its phosphorylation stimulated by collagen. In the present study, we investigated the effect of S1P on the collagen-induced platelet activation. S1P pretreatment markedly attenuated the collagen-induced aggregation. Co-stimulation with S1P and collagen suppressed collagen-induced platelet activation, but the effect was weaker than that of S1P-pretreatment. The collagen-stimulated secretion of platelet-derived growth factor (PDGF)-AB and the soluble CD40 ligand (sCD40L) release were significantly reduced by S1P. In addition, S1P suppressed the collagen-induced release of HSP27 as well as the phosphorylation of HSP27. S1P significantly suppressed the collagen-induced phosphorylation of p38 mitogen-activated protein kinase. S1P increased the levels of GTP-bound Gαi and GTP-bound Gα13 coupled to S1PPR1 and/or S1PR4. CYM50260, a selective S1PR4 Agonist, but not SEW2871, a selective S1PR1 Agonist, suppressed the collagen-stimulated platelet aggregation, PDGF-AB secretion and sCD40L release. In addition, CYM50260 reduced the release of phosphorylated-HSP27 by collagen as well as the phosphorylation of HSP27. The selective S1PR4 Antagonist CYM50358, which failed to affect collagen-induced HSP27 phosphorylation, reversed the S1P-induced attenuation of HSP27 phosphorylation by collagen. These results strongly suggest that S1P inhibits the collagen-induced human platelet activation through S1PR4 but not S1PR1.

Keywords

Collagen; HSP27; Phosphorylation; Platelet; Receptor; Sphingosine 1-phosphate.

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