Evidence map›Paper›PMID 25387834›Full record

Trial reportJournal of leukocyte biology2015

Proline-rich tyrosine kinase 2 controls PI3-kinase activation downstream of the T cell antigen receptor in human T cells.

Nicole M Chapman, Ashley N Yoder, Kathryn M Barbón, Mahmood Y Bilal, Sean F Connolly, Jon C D Houtman

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Journal of leukocyte biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. The integrin adhesome and control of anti-tumour immunity.Biochemical Society transactions · 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

6 authors at 1 institution in 1 country.

Nicole M Chapman*Interdisciplinary Graduate Program in Immunology and Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Ashley N Yoder*Interdisciplinary Graduate Program in Immunology and Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Kathryn M Barbón*Interdisciplinary Graduate Program in Immunology and Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Mahmood Y Bilal*Interdisciplinary Graduate Program in Immunology and Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Sean F Connolly*Interdisciplinary Graduate Program in Immunology and Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Jon C D Houtman*Interdisciplinary Graduate Program in Immunology and Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA jon-houtman@uiowa.edu.
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
PREDOCTORAL TRAINING PROGRAM IN IMMUNOLOGYT32AI007485 · NIAID · UNIVERSITY OF IOWA · PI Kevin L Legge · 1995 to 2026
$5.4M
Cooperative SH2 and SH3 domain-mediated interactions at the adaptor protein Grb2R01CA136729 · NCI · UNIVERSITY OF IOWA · PI HOUTMAN, JON C.D. · 2010 to 2014
$1.6M
NCI NIH HHS R01 CA136729NCI NIH HHS R01-CA136729NIAID NIH HHS T32 AI007485
6 · The paper itself

Abstract

TCR-induced signaling controls T cell activation that drives adaptive immunity against infections, but it can also induce dysfunctional T cell responses that promote pathologic disease. The PI3K pathway regulates many downstream effector responses after TCR stimulation. However, the molecular mechanisms that induce PI3K function downstream of the TCR are not fully understood. We have previously shown that Pyk2 is activated downstream of the TCR in a PI3K-independent manner. Although Pyk2 controls adhesion, proliferation, and cytokine production in T cells, the mechanisms by which it controls these processes are not known. In this study, we generated Pyk2-deficient human T cells to elucidate further the role that this kinase plays in TCR-induced effector functions and signaling. We observed that Pyk2 localized with the p85 regulatory subunit of PI3K at the LAT complex and that PI3K-dependent signaling was impaired in Pyk2-deficient T cells. Likewise, functions downstream of PI3K, including IFN-γ production and proliferation, were also suppressed in human T cells deficient in Pyk2. Collectively, these data demonstrate that Pyk2 is a critical regulator of PI3K function downstream of the TCR.

Indexed as

Cell ProliferationCell AdhesionClass Ia Phosphatidylinositol 3-KinaseEnzyme ActivationFemaleFocal Adhesion Kinase 2HumansInterferon-gammaMaleReceptors, Antigen, T-CellT-LymphocytesClass Ia Phosphatidylinositol 3-KinaseFocal Adhesion Kinase 2IFNG protein, humanInterferon-gammaReceptors, Antigen, T-CellAktp85 phosphorylation

Identifiers

PMID25387834
PMCPMC4304419
OpenAlexW2007772975

What OpenQuestion holds

Textmetadata
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.