Evidence map›Paper›PMID 10794715›Full record

ArticleThe Biochemical journal2000

Sphingosine 1-phosphate stimulates proliferation and migration of human endothelial cells possibly through the lipid receptors, Edg-1 and Edg-3.

T Kimura, T Watanabe, K Sato, J Kon, H Tomura, K Tamama, A Kuwabara, T Kanda, I Kobayashi, H Ohta and 2 more

Open access · greenAbstract read
In one paragraph

Article in The Biochemical journal, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
6.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

78 citing papers in PubMed, 233 citations in OpenAlex.

  1. Article
  2. Endothelial Surface Glycocalyx in Vascular Functions and Diseases.Advances in experimental medicine and biology · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. HDL and Endothelial Function.Advances in experimental medicine and biology · 2022
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Crossing signals: bioactive lipids in the microvasculature.American journal of physiology. Heart and circulatory physiology · 2020
    Review
  14. Sphingolipid Signature of Human Feto-Placental Vasculature in Preeclampsia.International journal of molecular sciences · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Bioactive lysolipids in cancer and angiogenesis.Pharmacology & therapeutics · 2019
    Review
  19. Review
  20. Article

18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

T KimuraLaboratory of Signal Transduction, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi 371-8512, Japan.
T Watanabe
K Sato
J Kon
H Tomura
K Tamama
A Kuwabara
T Kanda
I Kobayashi
H Ohta
M Ui
F Okajima
Gunma University · JPKirin (Japan) · JPTokyo Metropolitan Institute of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingosine 1-phosphate (S1P) stimulates thymidine incorporation (DNA synthesis), cell growth and cell migration in human aortic endothelial cells (HAECs). The extent of the S1P-induced responses are comparable to those stimulated by vascular endothelial growth factor, one of the most potent stimulators of angiogenesis. These responses to S1P were mimicked by dihydrosphingosine 1-phosphate, an S1P receptor agonist, and inhibited by pertussis toxin (PTX), an inactivator of G(i)/G(o)-proteins. S1P also induced activation of extracellular signal-regulated kinase (ERK) and p38 mitogen-activated protein kinase (p38 MAP kinase). The activation of these enzymes was inhibited again by PTX and also by suramin, a non-selective receptor antagonist. S1P-induced DNA synthesis and ERK activation were inhibited by PD98059, an ERK kinase inhibitor, but not by SB203580, a p38 MAP kinase inhibitor. In contrast, cell migration and p38 MAP kinase activation, in response to S1P, were inhibited by SB203580 but not by PD98059. In HAECs, high-affinity S1P binding activity and expression of Edg-1 and Edg-3 mRNA were detected. These results suggest that S1P might be a novel angiogenesis factor and that the lipid-induced proliferation and migration of endothelial cells are possibly mediated through cell-surface S1P receptors, Edg-1 and Edg-3, which are linked to signalling pathways.

Indexed as

I-kappa B ProteinsLysophospholipidsReceptors, Cell SurfaceReceptors, G-Protein-CoupledAntineoplastic AgentsBinding, CompetitiveCell DivisionCell MovementCells, CulturedDNADNA-Binding ProteinsEndothelium, VascularGTP-Binding ProteinsHumansImmediate-Early ProteinsMitogen-Activated Protein KinasesAntineoplastic AgentsDNADNA-Binding ProteinsGTP-Binding ProteinsI-kappa B ProteinsImmediate-Early ProteinsLysophospholipidsMitogen-Activated Protein KinasesNF-KappaB Inhibitor alphaNFKBIA protein, humanp38 Mitogen-Activated Protein KinasesPertussis ToxinReceptors, Cell SurfaceReceptors, G-Protein-CoupledReceptors, LysophospholipidRNA, MessengerSphingosinesphingosine 1-phosphateSuraminVirulence Factors, Bordetella

Identifiers

PMID10794715
PMCPMC1221037
OpenAlexW2166848649

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.