Evidence map›Paper›PMID 27566939›Full record

ArticleImmunity2016

Phosphoproteomic Analyses of Interleukin 2 Signaling Reveal Integrated JAK Kinase-Dependent and -Independent Networks in CD8(+) T Cells.

Sarah H Ross, Christina Rollings, Karen E Anderson, Phillip T Hawkins, Len R Stephens, Doreen A Cantrell

Open access · hybridAbstract read
In one paragraph

Article in Immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

58 citing papers in PubMed, 91 citations in OpenAlex.

  1. Review
  2. The moonlighting functions of glycolytic enzymes in tumorigenesis.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
  3. Review
  4. Dynamics and variegation in the Treg response to Interleukin-2.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. IRG1/Itaconate inhibits proliferation and promotes apoptosis of CD69Apoptosis : an international journal on programmed cell death · 2024
    Article
  9. IL-2 delivery to CD8Nature communications · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Resilient T-cell responses in patients with advanced cancers.International journal of hematology · 2023
    Review
  20. Review
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 2 institutions in 1 country.

Sarah H RossDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK.
Christina RollingsDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK.
Karen E AndersonInositide Laboratory, Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Phillip T HawkinsInositide Laboratory, Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Len R StephensInositide Laboratory, Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Doreen A CantrellDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK. Electronic address: d.a.cantrell@dundee.ac.uk.
Babraham Institute · GBUniversity of Dundee · GB

Funding

Biotechnology and Biological Sciences Research CouncilWellcome Trust 097418/Z/11/Z
6 · The paper itself

Abstract

Interleukin-2 (IL-2) is a fundamental cytokine that controls proliferation and differentiation of T cells. Here, we used high-resolution mass spectrometry to generate a comprehensive and detailed map of IL-2 protein phosphorylations in cytotoxic T cells (CTL). The data revealed that Janus kinases (JAKs) couple IL-2 receptors to the coordinated phosphorylation of transcription factors, regulators of chromatin, mRNA translation, GTPases, vesicle trafficking, and the actin and microtubule cytoskeleton. We identified an IL-2-JAK-independent SRC family Tyr-kinase-controlled signaling network that regulates ∼10% of the CTL phosphoproteome, the production of phosphatidylinositol (3,4,5)-trisphosphate (PIP3), and the activity of the serine/threonine kinase AKT. These data reveal a signaling framework wherein IL-2-JAK-controlled pathways coordinate with IL-2-independent networks of kinase activity and provide a resource toward the further understanding of the networks of protein phosphorylation that program CTL fate.

Indexed as

ActinsAnimalsCD8-Positive T-LymphocytesCell DifferentiationCell ProliferationGTP PhosphohydrolasesInterleukin-2Janus KinasesMicePhosphorylationProtein Serine-Threonine KinasesProteomeRNA, MessengerSignal TransductionTrans-ActivatorsActinsGTP PhosphohydrolasesInterleukin-2Janus KinasesProtein Serine-Threonine KinasesProteomeRNA, MessengerTrans-Activators

Identifiers

PMID27566939
PMCPMC5040828
OpenAlexW2512028013

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.