Evidence map›Paper›PMID 31413071›Full record

ArticleJournal of cell science2019

Distinct actin cytoskeleton behaviour in primary and immortalised T-cells.

Huw Colin-York, Sudha Kumari, Liliana Barbieri, Lena Cords, Marco Fritzsche

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 46 citations in OpenAlex.

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  13. Sourcing cells forFrontiers in medical technology · 2022
    Review
  14. Article
  15. Review
  16. Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells.Frontiers in cell and developmental biology · 2021
    Review
  17. Article
  18. Review
  19. Article
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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

5 authors at 2 institutions in 2 countries.

Huw Colin-YorkMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK.ORCID 0000-0002-6585-3237
Sudha KumariKoch Institute of Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge 02139, USA kumars04@mit.edu marco.fritzsche@rdm.ox.ac.uk.
Liliana BarbieriMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK.ORCID 0000-0002-1804-7451
Lena CordsMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK.
Marco FritzscheMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK kumars04@mit.edu marco.fritzsche@rdm.ox.ac.uk.ORCID 0000-0002-8712-7471
University of Oxford · GBMassachusetts Institute of Technology · US

Funding

Medical Research CouncilWellcome Trust 212343/Z/18/Z
6 · The paper itself

Abstract

Cytoskeletal actin dynamics are crucial for the activation of T-cells. Immortalised Jurkat T-cells have been the model system of choice to examine and correlate the dynamics of the actin cytoskeleton and the immunological synapse leading to T-cell activation. However, it has remained unclear whether immortalised cellular systems, such as Jurkat T-cells can recapitulate the cytoskeletal behaviour of primary T-cells. Studies delineating the cytoskeletal behaviour of Jurkat T-cells in comparison to primary T-cells are lacking. Here, we employ live-cell super-resolution microscopy to investigate the cytoskeletal actin organisation and dynamics of living primary and immortalised Jurkat T-cells at the appropriate spatiotemporal resolution. Under comparable activation conditions, we found differences in the architectural organisation and dynamics of Jurkat and primary mouse and human T-cells. Although the three main actin network architectures in Jurkat T-cells were reminiscent of primary T-cells, there were differences in the organisation and molecular mechanisms underlying these networks. Our results highlight mechanistic distinctions in the T-cell model system most utilised to study cytoskeletal actin dynamics.

Indexed as

Actin CytoskeletonActinsAnimalsGene Rearrangement, T-LymphocyteHumansImmunological SynapsesJurkat CellsLymphocyte ActivationMiceModels, BiologicalReceptors, Antigen, T-CellSignal TransductionT-LymphocytesActinsReceptors, Antigen, T-CellActin cytoskeletonImmune synapseJurkat cellsPrimary T-cells

Identifiers

PMID31413071
PMCPMC6898998
OpenAlexW2967293767

What OpenQuestion holds

Textmetadata
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.