Evidence map›Paper›PMID 33762632›Full record

ArticleScientific reports2021

Controlling T cells spreading, mechanics and activation by micropatterning.

Anaïs Sadoun, Martine Biarnes-Pelicot, Laura Ghesquiere-Dierickx, Ambroise Wu, Olivier Théodoly, Laurent Limozin, Yannick Hamon, Pierre-Henri Puech

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Advances in Regulating Cellular Behavior Using Micropatterns.The Yale journal of biology and medicine · 2023
    Review
  9. Light-inducible T cell engagers trigger, tune, and shape the activation of primary T cells.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. 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

8 authors at 3 institutions in 2 countries.

Anaïs SadounAdhesion and Inflammation Lab (LAI), Aix Marseille University, LAI UM 61, 13288, Marseille, France.
Martine Biarnes-PelicotAdhesion and Inflammation Lab (LAI), Aix Marseille University, LAI UM 61, 13288, Marseille, France.
Laura Ghesquiere-DierickxAdhesion and Inflammation Lab (LAI), Aix Marseille University, LAI UM 61, 13288, Marseille, France.
Ambroise WuCentre d'Immunologie de Marseille Luminy (CIML), Aix-Marseille University, CNRS, Inserm, CIML Marseille, 13288, Marseille, France.
Olivier ThéodolyAdhesion and Inflammation Lab (LAI), Aix Marseille University, LAI UM 61, 13288, Marseille, France.
Laurent LimozinAdhesion and Inflammation Lab (LAI), Aix Marseille University, LAI UM 61, 13288, Marseille, France.
Yannick HamonCentre d'Immunologie de Marseille Luminy (CIML), Aix-Marseille University, CNRS, Inserm, CIML Marseille, 13288, Marseille, France. hamon@ciml.univ-mrs.fr.
Pierre-Henri PuechAdhesion and Inflammation Lab (LAI), Aix Marseille University, LAI UM 61, 13288, Marseille, France. pierre-henri.puech@inserm.fr.
Aix-Marseille Université · FRCentre National de la Recherche Scientifique · FRHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We designed a strategy, based on a careful examination of the activation capabilities of proteins and antibodies used as substrates for adhering T cells, coupled to protein microstamping to control at the same time the position, shape, spreading, mechanics and activation state of T cells. Once adhered on patterns, we examined the capacities of T cells to be activated with soluble anti CD3, in comparison to T cells adhered to a continuously decorated substrate with the same density of ligands. We show that, in our hand, adhering onto an anti CD45 antibody decorated surface was not affecting T cell calcium fluxes, even adhered on variable size micro-patterns. Aside, we analyzed the T cell mechanics, when spread on pattern or not, using Atomic Force Microscopy indentation. By expressing MEGF10 as a non immune adhesion receptor in T cells we measured the very same spreading area on PLL substrates and Young modulus than non modified cells, immobilized on anti CD45 antibodies, while retaining similar activation capabilities using soluble anti CD3 antibodies or through model APC contacts. We propose that our system is a way to test activation or anergy of T cells with defined adhesion and mechanical characteristics, and may allow to dissect fine details of these mechanisms since it allows to observe homogenized populations in standardized T cell activation assays.

Indexed as

AnimalsBiomarkersCalciumCell AdhesionCell Line, TumorCell ShapeChemotaxis, LeukocyteEctopic Gene ExpressionHumansLeukocyte Common AntigensLymphocyte ActivationMolecular ImagingT-LymphocytesBiomarkersCalciumLeukocyte Common Antigens

Identifiers

PMID33762632
PMCPMC7991639
OpenAlexW3138575739

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.