Evidence map›Paper›PMID 26830463›Full record

ArticleeLife2016

Fibroblastic reticular cell-derived lysophosphatidic acid regulates confined intranodal T-cell motility.

Akira Takeda, Daichi Kobayashi, Keita Aoi, Naoko Sasaki, Yuki Sugiura, Hidemitsu Igarashi, Kazuo Tohya, Asuka Inoue, Erina Hata, Noriyuki Akahoshi and 12 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. GPCRs: emerging targets for novel T cell immune checkpoint therapy.Cancer immunology, immunotherapy : CII · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Lysophospholipid Mediators in Health and Disease.Annual review of pathology · 2022
    Review
  11. Article
  12. Article
  13. Review
  14. LPA and Autotaxin: Potential Drug Targets in Asthma?Cell biochemistry and biophysics · 2021
    Review
  15. Review
  16. Article
  17. Review
  18. The roles of autotaxin/lysophosphatidic acid in immune regulation and asthma.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2020
    Review
  19. Article
  20. Review
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

22 authors at 7 institutions in 3 countries.

Akira TakedaLaboratory of Immunodynamics, Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Daichi KobayashiLaboratory of Immunodynamics, Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Keita AoiWPI Immunology Frontier Research Center, Osaka University, Osaka, Japan.
Naoko SasakiLaboratory of Immunodynamics, Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Yuki SugiuraDepartment of Biochemistry, Keio University School of Medicine, Tokyo, Japan.
Hidemitsu IgarashiDepartment of Immunology, Graduate School of Medicine, Akita University, Akita, Japan.
Kazuo TohyaDepartment of Anatomy, Kansai University of Health Sciences, Awaji, Japan.
Asuka InoueLaboratory of Molecular and Cellular Biochemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.
Erina HataLaboratory of Immunodynamics, Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Noriyuki AkahoshiDepartment of Immunology, Graduate School of Medicine, Akita University, Akita, Japan.
Haruko HayasakaLaboratory of Immunodynamics, Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Junichi KikutaWPI Immunology Frontier Research Center, Osaka University, Osaka, Japan.
Elke ScandellaInstitute of Immunobiology, Kantonal Hospital St. Gallen, St. Gallen, Switzerland.
Burkhard LudewigInstitute of Immunobiology, Kantonal Hospital St. Gallen, St. Gallen, Switzerland.
Satoshi IshiiDepartment of Immunology, Graduate School of Medicine, Akita University, Akita, Japan.
Junken AokiLaboratory of Molecular and Cellular Biochemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.
Makoto SuematsuDepartment of Biochemistry, Keio University School of Medicine, Tokyo, Japan.
Masaru IshiiWPI Immunology Frontier Research Center, Osaka University, Osaka, Japan.
Kiyoshi TakedaWPI Immunology Frontier Research Center, Osaka University, Osaka, Japan.
Sirpa JalkanenMediCity Research Laboratory, University of Turku, Turku, Finland.
Masayuki MiyasakaLaboratory of Immunodynamics, Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Eiji UmemotoLaboratory of Immunodynamics, Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, Osaka, Japan.
Osaka University · JPAkita University · JPUniversity of Turku · FIJapan Science and Technology Agency · JPKantonsspital St. Gallen · CHTohoku University · JPKansai University of Nursing and Health Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymph nodes (LNs) are highly confined environments with a cell-dense three-dimensional meshwork, in which lymphocyte migration is regulated by intracellular contractile proteins. However, the molecular cues directing intranodal cell migration remain poorly characterized. Here we demonstrate that lysophosphatidic acid (LPA) produced by LN fibroblastic reticular cells (FRCs) acts locally to LPA2 to induce T-cell motility. In vivo, either specific ablation of LPA-producing ectoenzyme autotaxin in FRCs or LPA2 deficiency in T cells markedly decreased intranodal T cell motility, and FRC-derived LPA critically affected the LPA2-dependent T-cell motility. In vitro, LPA activated the small GTPase RhoA in T cells and limited T-cell adhesion to the underlying substrate via LPA2. The LPA-LPA2 axis also enhanced T-cell migration through narrow pores in a three-dimensional environment, in a ROCK-myosin II-dependent manner. These results strongly suggest that FRC-derived LPA serves as a cell-extrinsic factor that optimizes T-cell movement through the densely packed LN reticular network.

Indexed as

Cell MovementAnimalsFibroblastsLysophospholipidsMice, Inbred C57BLMolecular Sequence DatarhoA GTP-Binding ProteinSequence Analysis, DNAT-Lymphocyteslysophosphatidic acidLysophospholipidsrhoA GTP-Binding Proteincell biologyFibroblastic reticular cellimmunologyLymph nodeLymphocyte migrationLysophospholipidmouse

Identifiers

PMID26830463
PMCPMC4755752
OpenAlexW2257922556

What OpenQuestion holds

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LicenceCC BY
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.