Evidence map›Paper›PMID 35757762›Full record

ArticleFrontiers in immunology2022

Ena/VASP Protein-Mediated Actin Polymerization Contributes to Naïve CD8

Monique M Waldman, Jeremy T Rahkola, Ashton L Sigler, Jeffrey W Chung, Benjamin A S Willett, Ross M Kedl, Rachel S Friedman, Jordan Jacobelli

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
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  4. Batf3Cell reports · 2024
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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

8 authors at 1 institution in 1 country.

Monique M WaldmanDepartment of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Jeremy T RahkolaRocky Mountain Regional Veterans Affairs (VA) Medical Center, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Ashton L SiglerDepartment of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Jeffrey W ChungDepartment of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Benjamin A S WillettDepartment of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Ross M KedlDepartment of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Rachel S FriedmanDepartment of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Jordan JacobelliDepartment of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
University of Colorado Anschutz Medical Campus · US

Funding

University of Colorado Anschutz Medical Campus DRCP30DK116073 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LORI SUSSEL · 2020 to 2026
$10.8M
TRAINING PROGRAM IN IMMUNOLOGYT32AI007405 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Laurel L Lenz, Raul Martin Torres · 1991 to 2026
$10.5M
MerTK Mediated T Cell Suppression in the Pancreatic Islets During Type 1 DiabetesR01DK111733 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Rachel S Friedman · 2017 to 2026
$4.1M
Regulation of T Cell Extravasation and Activation by Ena/Vasp ProteinsR01AI125553 · NIAID · UNIVERSITY OF COLORADO DENVER · PI JACOBELLI, JORDAN · 2017 to 2021
$2.0M
NIAID NIH HHS R01 AI125553NIAID NIH HHS T32 AI007405NIDDK NIH HHS P30 DK116073NIDDK NIH HHS R01 DK111733
6 · The paper itself

Abstract

Naïve T cell activation in secondary lymphoid organs such as lymph nodes (LNs) occurs upon recognition of cognate antigen presented by antigen presenting cells (APCs). T cell activation requires cytoskeleton rearrangement and sustained interactions with APCs. Enabled/vasodilator-stimulated phosphoprotein (Ena/VASP) proteins are a family of cytoskeletal effector proteins responsible for actin polymerization and are frequently found at the leading edge of motile cells. Ena/VASP proteins have been implicated in motility and adhesion in various cell types, but their role in primary T cell interstitial motility and activation has not been explored. Our goal was to determine the contribution of Ena/VASP proteins to T cell-APC interactions, T cell activation, and T cell expansion

Indexed as

ActinsCD8-Positive T-LymphocytesCell Adhesion MoleculesMicrofilament ProteinsPhosphoproteinsT-LymphocytesAnimalsCytoskeletal ProteinsLymphocyte ActivationMicePolymerizationVasodilator-Stimulated PhosphoproteinActinsCell Adhesion MoleculesCytoskeletal ProteinsMicrofilament ProteinsPhosphoproteinsVasodilator-Stimulated PhosphoproteincytoskeletonEVLimmunological synapseT cellT cell activationT cell motilitytwo-photon microscopyVASP

Identifiers

PMID35757762
PMCPMC9222560
OpenAlexW4281735665

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.