Evidence map›Paper›PMID 29563527›Full record

ArticleScientific reports2018

MFSD2B is a sphingosine 1-phosphate transporter in erythroid cells.

Naoki Kobayashi, Shoko Kawasaki-Nishi, Masato Otsuka, Yu Hisano, Akihito Yamaguchi, Tsuyoshi Nishi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

52 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
  2. Observational
  3. Review
  4. Erythrocytes as a Source of Exerkines.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Article
  7. Review
  8. Regulation of cellular and systemic sphingolipid homeostasis.Nature reviews. Molecular cell biology · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Mfsd2a utilizes a flippase mechanism to mediate omega-3 fatty acid lysolipid transport.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Article
  17. Sphingolipids in Atherosclerosis: Chimeras in Structure and Function.International journal of molecular sciences · 2022
    Review
  18. Article
  19. Review
  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

6 authors at 4 institutions in 1 country.

Naoki KobayashiDepartment of Biochemistry, Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata, Osaka, 573-0101, Japan.
Shoko Kawasaki-NishiDepartment of Biomolecular Science and Regulation, Osaka University, Ibaraki, Osaka, 567-0047, Japan.
Masato OtsukaDepartment of Biochemistry, Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata, Osaka, 573-0101, Japan.
Yu HisanoDepartment of Biomolecular Science and Regulation, Osaka University, Ibaraki, Osaka, 567-0047, Japan.
Akihito YamaguchiDepartment of Cell Membrane Structural Biology, Institute of Scientific and Industrial Research, Osaka University, Ibaraki, Osaka, 567-0047, Japan.ORCID 0000-0001-8083-7609
Tsuyoshi NishiDepartment of Biomolecular Science and Regulation, Osaka University, Ibaraki, Osaka, 567-0047, Japan. tnishi@sanken.osaka-u.ac.jp.
Setsunan University · JPThe University of Osaka · JPOsaka Research Institute of Industrial Science and Technology · JPOsaka University of Economics · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingosine 1-phosphate (S1P) is an intercellular signaling molecule present in blood. Erythrocytes have a central role in maintaining the S1P concentration in the blood stream. We previously demonstrated that S1P is exported from erythrocytes by a glyburide-sensitive S1P transporter. However, the gene encoding the S1P transporter in erythrocytes is unknown. In this study, we found that the mouse erythroid cell line, MEDEP-E14, has S1P export activity and exhibits properties that are consistent with those of erythrocytes. Using microarray analysis of MEDEP-E14 cells and its parental cell line, E14TG2a, we identified several candidate genes for S1P export activity. Of those genes, only one gene, Mfsd2b, showed S1P transport activity. The properties of S1P release by MFSD2B were similar to those in erythrocytes. Moreover, knockout of MFSD2B in MEDEP-E14 cells decreased S1P export from the cells. These results strongly suggest that MFSD2B is a novel S1P transporter in erythroid cells.

Indexed as

AnimalsCell LineCHO CellsCricetulusErythroid CellsGene Knockout TechniquesLysophospholipidsMembrane ProteinsMiceMicroarray AnalysisPhosphotransferases (Alcohol Group Acceptor)Recombinant ProteinsSphingosineSphingosine KinaseLysophospholipidsMembrane ProteinsMfsd2b protein, humanMfsd2b protein, mousePhosphotransferases (Alcohol Group Acceptor)Recombinant ProteinsSphingosinesphingosine 1-phosphateSphingosine Kinase

Identifiers

PMID29563527
PMCPMC5862976
OpenAlexW2806198870

What OpenQuestion holds

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Registered trials

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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.