Evidence map›Paper›PMID 27936140›Full record

ArticlePloS one2016

Time-Dependent Regulation of IL-2R α-Chain (CD25) Expression by TCR Signal Strength and IL-2-Induced STAT5 Signaling in Activated Human Blood T Lymphocytes.

Alla N Shatrova, Elena V Mityushova, Irina O Vassilieva, Nikolay D Aksenov, Valery V Zenin, Nikolay N Nikolsky, Irina I Marakhova

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

42 citing papers in PubMed, 66 citations in OpenAlex.

  1. The Antigen Presenting Potential of CD21Frontiers in immunology · 2020
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  9. Advanced Identification of Trypanosoma cruzi-Specific CD4Methods in molecular biology (Clifton, N.J.) · 2026
    Article
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  15. Review
  16. Extracellular Delivery of Functional Mitochondria Rescues the Dysfunction of CD4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  17. Article
  18. Article
  19. Review
  20. 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

7 authors at 1 institution in 1 country.

Alla N ShatrovaDepartment of Intracellular Signaling and Transport, Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russia.
Elena V MityushovaDepartment of Intracellular Signaling and Transport, Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russia.
Irina O VassilievaDepartment of Intracellular Signaling and Transport, Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russia.
Nikolay D AksenovDepartment of Intracellular Signaling and Transport, Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russia.
Valery V ZeninDepartment of Intracellular Signaling and Transport, Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russia.
Nikolay N NikolskyDepartment of Intracellular Signaling and Transport, Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russia.
Irina I MarakhovaDepartment of Intracellular Signaling and Transport, Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russia.
Institute of Cytology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of the IL-2R α-chain (IL-2Rα) is regulated at the transcriptional level via TCR- and IL-2R-signaling. The question is how to precede in time the activation signals to induce the IL-2Rα expression in native primary T cells. By comparing the effects of selective drugs on the dynamics of CD25 expression during the mitogen stimulation of human peripheral blood lymphocytes, we identified distinct Src- and JAK-dependent stages of IL-2Rα upregulation. PP2, a selective inhibitor of TCR-associated Src kinase, prevents CD25 expression at initial stages of T cell activation, prior to the cell growth. This early IL-2Rα upregulation underlies the T cell competence and the IL-2 responsiveness. We found that the activated with "weak" mitogen, the population of blood lymphocytes has some pool of competent CD25+ cells bearing a high affinity IL-2R. A distinct pattern of IL-2R signaling in resting and competent T lymphocytes has been shown. Based on the inhibitory effect of WHI-P131, a selective drug of JAK3 kinase activity, we concluded that in quiescent primary T lymphocytes, the constitutive STAT3 and the IL-2-induced prolonged STAT5 activity (assayed by tyrosine phosphorylation) is mostly JAK3-independent. In competent T cells, in the presence of IL-2 JAK3/STAT5 pathway is switched to maintain the higher and sustained IL-2Rα expression as well as cell growth and proliferation. We believe that understanding the temporal coordination of antigen- and cytokine-evoked signals in primary T cells may be useful for improving immunotherapeutic strategies.

Indexed as

Blotting, WesternCell CycleCell ProliferationCells, CulturedGene Expression RegulationHumansInterleukin-2Interleukin-2 Receptor alpha SubunitJanus Kinase 3Lymphocyte ActivationPhosphorylationPhytohemagglutininsQuinazolinesReceptors, Antigen, T-CellReverse Transcriptase Polymerase Chain ReactionSignal TransductionInterleukin-2Interleukin-2 Receptor alpha SubunitJAK3 protein, humanJanus Kinase 3PhytohemagglutininsQuinazolinesReceptors, Antigen, T-CellSTAT5 Transcription FactorWHI P131

Identifiers

PMID27936140
PMCPMC5172478
OpenAlexW2560324574

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.