Evidence map›Paper›PMID 26514620›Full record

ArticleEuropean journal of immunology2016

p(⁷⁰S⁶K¹) in the TORC1 pathway is essential for the differentiation of Th17 Cells, but not Th1, Th2, or Treg cells in mice.

Carl Y Sasaki, Gang Chen, Rachel Munk, Erez Eitan, Jennifer Martindale, Dan L Longo, Paritosh Ghosh

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. Trial
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  12. PIR-B Regulates CD4Cellular and molecular gastroenterology and hepatology · 2021
    Article
  13. The Ups and Downs of Metabolism during the Lifespan of a T Cell.International journal of molecular sciences · 2020
    Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Metabolic regulation of TMolecular immunology · 2019
    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 3 institutions in 1 country.

Carl Y SasakiLaboratory of Genetics, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Gang ChenLaboratory of Genetics, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Rachel MunkLaboratory of Genetics, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Erez EitanLaboratory of Neurosciences, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Jennifer MartindaleLaboratory of Genetics, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Dan L LongoLaboratory of Genetics, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Paritosh GhoshLaboratory of Genetics, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
National Institutes of Health · USInstitute on Aging · USNational Institute on Aging · US

Funding

Rapamycin-sensitive pathway of T cell ActivationZIAAG000115 · NIA · NATIONAL INSTITUTE ON AGING · PI GHOSH, PARITOSH · 2009 to 2016
$4.1M
Intramural NIH HHS Z99 AG999999
6 · The paper itself

Abstract

The TORC1 pathway is necessary for ribosomal biogenesis and initiation of protein translation. Furthermore, the differentiation of Th1 and Th17 cells requires TORC1 activity. To investigate the role of the TORC1 pathway in the differentiation of Th1 and/or Th17 cells in more detail, we compared the differentiation capacity of naïve T cells from wild type and p70(S6K1) knockout mice. Expression of many of the genes associated with Th17-cell differentiation, such as IL17a, IL17f, and IL-23R, were reduced in p70(S6K1) knockout mice. In contrast, the development of Th1, Th2, and Treg cells was unaffected in the absence of p70(S6K1) . Furthermore, expression of the major transcription factor in Th17-cell differentiation, retinoic acid receptor-related orphan receptor gamma T, remained unchanged. However, the acetylation of histone 3 at the promoters of IL17a and IL17f was reduced in the absence of p70(S6K1) . In accordance with the in vitro data, the kinetics, but not the development, of EAE was affected with the loss of p70(S6K1) expression. Collectively, our findings suggested that both in vitro and in vivo differentiation of Th17 cells were positively regulated by p70(S6K1) .

Indexed as

AnimalsCell DifferentiationChromatin ImmunoprecipitationEncephalomyelitis, Autoimmune, ExperimentalFemaleFlow CytometryImmunoblottingLymphocyte ActivationMechanistic Target of Rapamycin Complex 1MiceMice, KnockoutMultiprotein ComplexesRibosomal Protein S6 Kinases, 70-kDaTh17 CellsTh1 CellsTh2 CellsMechanistic Target of Rapamycin Complex 1Multiprotein ComplexesRibosomal Protein S6 Kinases, 70-kDaTOR Serine-Threonine KinasesIL-17mTORp70S6K1T-cell differentiation

Identifiers

PMID26514620
PMCPMC5858723
OpenAlexW2133278646

What OpenQuestion holds

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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.