Evidence map›Paper›PMID 26481905›Full record

ArticleTraffic (Copenhagen, Denmark)2016

Endocytosis of Ligand-Activated Sphingosine 1-Phosphate Receptor 1 Mediated by the Clathrin-Pathway.

Patrick M Reeves, Yuan-Lin Kang, Tom Kirchhausen

Open access · bronzeAbstract read
In one paragraph

Article in Traffic (Copenhagen, Denmark), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Transmembrane protein CD69 acts as an S1PR1 agonist.bioRxiv : the preprint server for biology · 2023
    Article
  7. aPC/PAR1 confers endothelial anti-apoptotic activity via a discrete, β-arrestin-2-mediated SphK1-S1PR1-Akt signaling axis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Tetraspanin CD82 regulates S1PRStem cell reports · 2021
    Article
  9. Proton-gated coincidence detection is a common feature of GPCR signaling.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Article
  11. Article
  12. Morpholino Analogues of Fingolimod as Novel and Selective S1PInternational journal of molecular sciences · 2020
    Article
  13. Post-translational modifications of S1PR1 and endothelial barrier regulation.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2020
    Review
  14. Glycosylation and raft endocytosis in cancer.Cancer metastasis reviews · 2020
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. S1PBioscience reports · 2018
    Article
  20. Article
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

3 authors at 2 institutions in 1 country.

Patrick M ReevesDepartment of Cell Biology, Harvard Medical School and Program in Cellular and Molecular Medicine at Boston Children's Hospital, Boston, MA, USA.
Yuan-Lin KangDepartment of Cell Biology, Harvard Medical School and Program in Cellular and Molecular Medicine at Boston Children's Hospital, Boston, MA, USA.
Tom KirchhausenDepartment of Cell Biology, Harvard Medical School and Program in Cellular and Molecular Medicine at Boston Children's Hospital, Boston, MA, USA.
Boston Children's Hospital · USHarvard University · US

Funding

Dynamics of Clathrin Coat Formation in CellsR01GM075252 · NIGMS · IMMUNE DISEASE INSTITUTE, INC. · PI KIRCHHAUSEN, TOMAS · 2005 to 2018
$4.6M
NIGMS NIH HHS GM-075252NIGMS NIH HHS R01 GM075252
6 · The paper itself

Abstract

The sphingosine 1-phosphate receptor 1 (S1PR1) is one of five G protein-coupled receptors activated by the lipid sphingosine 1-phosphate (S1P). Stimulation of S1PR1 by binding S1P or the synthetic agonist FTY720P results in rapid desensitization, associated in part with depletion of receptor from the cell surface. We report here combining spinning disc confocal fluorescence microscopy and flow cytometry to show that rapid internalization of activated S1PR1 relies on a functional clathrin-mediated endocytic pathway. Uptake of activated S1PR1 was strongly inhibited in cells disrupted in their clathrin-mediated endocytosis by depleting clathrin or AP-2 or by treating cells with dynasore-OH. The uptake of activated S1P1R was strongly inhibited in cells lacking both β-arrestin 1 and β-arrestin 2, indicating that activated S1PR1 follows the canonical route of endocytosis for G-protein coupled receptor's (GPCR)'s.

Indexed as

EndocytosisAnimalsArrestinsbeta-Arrestin 1beta-Arrestin 2beta-ArrestinsClathrinHEK293 CellsHeLa CellsHumansMiceOrganophosphatesReceptors, LysosphingolipidSphingosineSphingosine-1-Phosphate ReceptorsARRB1 protein, humanArrb1 protein, mouseARRB2 protein, humanArrb2 protein, mouseArrestinsbeta-Arrestin 1beta-Arrestin 2beta-ArrestinsClathrinFTY 720POrganophosphatesReceptors, LysosphingolipidS1PR1 protein, humanSphingosineSphingosine-1-Phosphate ReceptorsclathrindownregulationG-protein coupled receptorsvesicular traffic

Identifiers

PMID26481905
PMCPMC4688054
OpenAlexW1810974063

What OpenQuestion holds

Textmetadata
LicenceTDM
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.