Evidence map›Paper›PMID 30279692›Full record

ArticleFrontiers in immunology2018

T Cells on Engineered Substrates: The Impact of TCR Clustering Is Enhanced by LFA-1 Engagement.

Emmanuelle Benard, Jacques A Nunès, Laurent Limozin, Kheya Sengupta

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Tetraspanin-5-mediated MHC class I clustering is required for optimal CD8 T cell activation.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Review
  7. Article
  8. Review
  9. Unraveling the mechanobiology of immune cells.Current opinion in biotechnology · 2020
    Review
  10. Review
  11. Article
  12. Biphasic mechanosensitivity of T cell receptor-mediated spreading of lymphocytes.Proceedings of the National Academy of Sciences of the United States of America · 2019
    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

4 authors at 3 institutions in 1 country.

Emmanuelle BenardCNRS, CINaM UMR 7325, Aix-Marseille Université, Marseille, France.
Jacques A NunèsCNRS, UMR7258, Centre de Recherche en Cancerologie de Marseille, Immunity and Cancer Team, Institut Paoli-Calmettes, Inserm, U1068, Aix-Marseille Université UM 105, Marseille, France.
Laurent LimozinLAI, CNRS UMR 7333, INSERM UMR 1067, Aix-Marseille Université, Marseille, France.
Kheya SenguptaCNRS, CINaM UMR 7325, Aix-Marseille Université, Marseille, France.
Centre National de la Recherche Scientifique · FRAix-Marseille Université · FRCentre Interdisciplinaire de Nanoscience de Marseille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We created APC-mimetic synthetic substrates to study the impact of ligand clustering on T cell activation and spreading. The substrates exhibit antibodies directed against the TCR-complex in the form of a patterned array of sub micrometric dots surrounded by a fluid supported lipid bilayer (SLB) which may itself be functionalized with another bio-molecule. We show that for T cell adhesion mediated by T cell receptor (TCR) alone, in the patterned, but not in the corresponding homogeneous controls, the TCR, ZAP-70 and actin are present in the form of clusters or patches that co-localize with the ligand-dots. However, global cell scale parameters like cell area and actin distribution are only weakly impacted by ligand clustering. In presence of ICAM-1 - the ligand of the T cell integrin LFA-1 - on the SLB, the TCR is still clustered due to the patterning of its ligands, but now global parameters are also impacted. The actin organization changes to a peripheral ring, resembling the classical actin distribution seen on homogeneous substrates, the patterned membrane topography disappears and the membrane is flat, whereas the cell area increases significantly. These observations taken together point to a possible pivotal role for LFA-1 in amplifying the effect of TCR-clustering. No such effect is evident for co-engagement of CD28, affected

Indexed as

ActinsAntigen-Presenting CellsBiomimeticsCD28 AntigensHumansIntercellular Adhesion Molecule-1Jurkat CellsLipid BilayersLymphocyte ActivationLymphocyte Function-Associated Antigen-1Multiprotein ComplexesReceptor AggregationReceptor Cross-TalkReceptors, Antigen, T-CellSignal TransductionT-LymphocytesActinsCD28 AntigensIntercellular Adhesion Molecule-1Lipid BilayersLymphocyte Function-Associated Antigen-1Multiprotein ComplexesReceptors, Antigen, T-CellZAP70 protein, humanZAP-70 Protein-Tyrosine Kinaseactin organizationcell spreadingco-stimulationprotein nano-patterningsurface bio-engineeringT cell adhesionTCR micro-clustersZAP-70 clusters

Identifiers

PMID30279692
PMCPMC6154019
OpenAlexW2891659622

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.