Evidence map›Paper›PMID 26634899›Full record

ArticleScientific reports2015

Differential effect of DJ-1/PARK7 on development of natural and induced regulatory T cells.

Yogesh Singh, Hong Chen, Yuetao Zhou, Michael Föller, Tak W Mak, Madhuri S Salker, Florian Lang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
11.4field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Journal of immunology research · 2023
    Article
  7. Review
  8. Article
  9. PARK7/DJ-1 as a Therapeutic Target in Gut-Brain Axis Diseases.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Review
  12. Review
  13. An immunodominant NPNature immunology · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  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

7 authors at 2 institutions in 2 countries.

Yogesh SinghDepartment of Physiology I, Eberhard-Karls-University of Tübingen, Tübingen, D-72076, Germany.
Hong ChenDepartment of Physiology I, Eberhard-Karls-University of Tübingen, Tübingen, D-72076, Germany.
Yuetao ZhouDepartment of Physiology I, Eberhard-Karls-University of Tübingen, Tübingen, D-72076, Germany.
Michael FöllerDepartment of Physiology I, Eberhard-Karls-University of Tübingen, Tübingen, D-72076, Germany.
Tak W MakCampbell Family Institute for Breast Cancer Research, Ontario Cancer Institute, UHN, 620 University Ave Toronto, M5G 2C1, Canada.
Madhuri S SalkerDepartment of Physiology I, Eberhard-Karls-University of Tübingen, Tübingen, D-72076, Germany.
Florian LangDepartment of Physiology I, Eberhard-Karls-University of Tübingen, Tübingen, D-72076, Germany.
University of Tübingen · DEOntario Institute for Cancer Research · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cells (Tregs) are essential for maintaining an effective immune tolerance and a homeostatic balance of various other immune cells. To manipulate the immune response during infections and autoimmune disorders, it is essential to know which genes or key molecules are involved in the development of Tregs. Transcription factor Foxp3 is required for the development of Tregs and governs most of the suppressive functions of these cells. Inhibited PI3K/AKT/mTOR signalling is critical for Foxp3 stability. Previous studies have suggested that DJ-1 or PARK7 protein is a positive regulator of the PI3K/AKT/mTOR pathway by negatively regulating the activity of PTEN. Thus, we hypothesised that a lack of DJ-1 could promote the development of Tregs. As a result, loss of DJ-1 decreased the total CD4(+) T cell numbers but increased the fraction of thymic and peripheral nTregs. In contrast, Foxp3 generation was not augmented following differentiation of DJ-1-deficient naïve CD4(+) T cells. DJ-1-deficient-iTregs were imperfect in replication, proliferation and more prone to cell death. Furthermore, DJ-1 deficient iTregs were less sensitive to pSmad2 and pStat5 signalling but had activated AKT/mTOR signalling. These observations reveal an unexpected differential role of DJ-1 in the development of nTregs and iTregs.

Indexed as

AnimalsCD4-Positive T-LymphocytesCell DifferentiationForkhead Transcription FactorsImmune ToleranceIntracellular Signaling Peptides and ProteinsMiceMice, KnockoutOncogene ProteinsPhosphatidylinositol 3-KinasesProtein Deglycase DJ-1Proto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSignal TransductionT-Lymphocytes, RegulatoryTOR Serine-Threonine KinasesAkt1 protein, mouseForkhead Transcription FactorsFoxp3 protein, mouseIntracellular Signaling Peptides and ProteinsmTOR protein, mouseOncogene ProteinsPARK7 protein, humanPhosphatidylinositol 3-KinasesProtein Deglycase DJ-1Proto-Oncogene Proteins c-aktPTEN PhosphohydrolaseTOR Serine-Threonine Kinases

Identifiers

PMID26634899
PMCPMC4669505
OpenAlexW2277439873

What OpenQuestion holds

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LicenceCC BY
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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.