Evidence map›Paper›PMID 21148815›Full record

ArticleBlood2011

Differential requirements for the Ets transcription factor Elf-1 in the development of NKT cells and NK cells.

Hak-Jong Choi, Yanbiao Geng, Hoonsik Cho, Sha Li, Pramod Kumar Giri, Kyrie Felio, Chyung-Ru Wang

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

39 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Elf1 Deficiency Impairs Macrophage Development in Zebrafish Model Organism.International journal of molecular sciences · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Self-Renewing Islet TCF1Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  16. microRNA dynamic expression regulates invariant NKT cells.Cellular and molecular life sciences : CMLS · 2021
    Review
  17. Mitochondrial metabolism is essential for invariant natural killer T cell development and function.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. Article
  19. Article
  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.

Hak-Jong ChoiDepartment of Microbiology and Immunology, Northwestern University, Chicago, IL 60611, USA.
Yanbiao Geng
Hoonsik Cho
Sha Li
Pramod Kumar Giri
Kyrie Felio
Chyung-Ru Wang
Northwestern University · US

Funding

The Regulation and Function of Murine CD1 MoleculesR01AI043407 · NIAID · UNIVERSITY OF CHICAGO · PI WANG, CHYUNG-RU · 1998 to 2017
$5.2M
NIAID NIH HHS R01 AI043407NIAID NIH HHS R01 AI43407
6 · The paper itself

Abstract

E26 Transformation specific (Ets) family transcription factors control the expression of a large number of genes regulating hematopoietic cell development and function. Two such transcription factors, Ets-1 and myeloid Elf-1-like factor (MEF), have been shown to play critical roles in both natural killer (NK)- and NKT-cell development, but not in the development of conventional T cells. In this study, we address the role of E74-like factor 1 (Elf-1), another Ets family transcription factor that is closely related to MEF but divergent from Ets-1, in NK- and NKT-cell development using Elf-1-deficient (Elf-1(-/-)) mice. Whereas the proportion of NK cells in Elf-1(-/-) mice was normal, the proportion of NKT cells was significantly reduced in the thymus and periphery of Elf-1(-/-) mice compared with wild-type (WT) mice. Although Ets-1-deficient mice lack NKT cells altogether, Elf-1(-/-) mice exhibited only a partial block in NKT-cell development caused by a cell-intrinsic defect in the selection, survival, and maturation of NKT cells. In addition, residual NKT cells found in Elf-1(-/-) mice produced less cytokine upon antigen stimulation compared with WT NKT cells. Our data demonstrate that Elf-1 plays an important and nonredundant role in the development and function of NKT cells, but is not involved in NK-cell development.

Indexed as

AnimalsAntigen PresentationAntigens, CD1dCell DifferentiationCell SurvivalCytokinesDNA-Binding ProteinsGenes, T-Cell Receptor alphaIn Vitro TechniquesKiller Cells, NaturalMiceMice, CongenicMice, Inbred C57BLMice, KnockoutNatural Killer T-CellsNuclear ProteinsAntigens, CD1dCytokinesDNA-Binding ProteinsElf1 protein, mouseElf4 protein, mouseEts1 protein, mouseNuclear ProteinsProto-Oncogene Protein c-ets-1Transcription Factors

Identifiers

PMID21148815
PMCPMC3056637
OpenAlexW2334436011

What OpenQuestion holds

Textmetadata
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.