Evidence map›Paper›PMID 24123679›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Increased level of E protein activity during invariant NKT development promotes differentiation of invariant NKT2 and invariant NKT17 subsets.

Taishan Hu, Hongcheng Wang, Amie Simmons, Sandra Bajaña, Ying Zhao, Susan Kovats, Xiao-Hong Sun, Jose Alberola-Ila

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. T Cell Development: From T-Lineage Specification to Intrathymic Maturation.Advances in experimental medicine and biology · 2025
    Review
  3. Review
  4. Development of αβ T Cells with Innate Functions.Advances in experimental medicine and biology · 2022
    Article
  5. ILC Differentiation in the Thymus.Advances in experimental medicine and biology · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Id2 Collaborates with Id3 To Suppress Invariant NKT and Innate-like Tumors.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  13. Article
  14. Transcriptional regulator Bhlhe40 works as a cofactor of T-bet in the regulation of IFN-γ production in iNKT cells.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  15. Development of invariant natural killer T cells.Current opinion in immunology · 2016
    Review
  16. Review
  17. Article
  18. Review
  19. 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

8 authors.

Taishan HuImmunobiology and Cancer Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104.
Hongcheng Wang
Amie Simmons
Sandra Bajaña
Ying Zhao
Susan Kovats
Xiao-Hong Sun
Jose Alberola-Ila

Funding

Notch-induced protein degradation in lymphopoiesisR01AI056129 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI SUN, XIAO-HONG · 2003 to 2013
$3.8M
Role of GATA-3 During CD4/CD8 Lineage CommitmentR01AI059302 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI ALBEROLA-ILA, JOSE · 2005 to 2009
$1.7M
Regulation of NKT cell development and function by c-MybR21AI088546 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI ALBEROLA-ILA, JOSE · 2010 to 2011
$446k
NIAID NIH HHS AI059302NIAID NIH HHS AI56129NIAID NIH HHS R01 AI056129NIAID NIH HHS R01 AI059302NIAID NIH HHS R21 AI088546
6 · The paper itself

Abstract

E protein transcription factors and their natural inhibitors, Id proteins, play critical and complex roles during lymphoid development. In this article, we report that partial maintenance of E protein activity during positive selection results in a change in the cell fate determination of developing iNKT cells, with a block in the development of iNKT1 cells and a parallel increase in the iNKT2 and iNKT17 subsets. Because the expression levels of the transcription factors that drive these alternative functional fates (GATA-3, RORγT, T-bet, and Runx-3) are not altered, our results suggest that E protein activity controls a novel checkpoint that regulates the number of iNKT precursors that choose each fate.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationCell ProliferationCells, CulturedCore Binding Factor Alpha 3 SubunitInterferon-gammaInterleukin-2 Receptor beta SubunitLymphocyte ActivationLymphocyte SubsetsMiceMice, Inbred C57BLMice, TransgenicNatural Killer T-CellsRNA, UntranslatedSignal TransductionBasic Helix-Loop-Helix ProteinsCore Binding Factor Alpha 3 SubunitGt(ROSA)26Sor non-coding RNA, mouseInterferon-gammaInterleukin-2 Receptor beta SubunitRNA, UntranslatedRunx3 protein, mouseT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID24123679
PMCPMC3832958

What OpenQuestion holds

Textmetadata
LicenceTDM
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.