Evidence map›Paper›PMID 19169262›Full record

ArticleNature immunology2009

The gene encoding early growth response 2, a target of the transcription factor NFAT, is required for the development and maturation of natural killer T cells.

Vanja Lazarevic, Alfred J Zullo, Michelle N Schweitzer, Tracy L Staton, Elena M Gallo, Gerald R Crabtree, Laurie H Glimcher

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

109 citing papers in PubMed, 161 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Invariant natural killer T cells in lung diseases.Experimental & molecular medicine · 2023
    Review
  6. Article
  7. Article
  8. Markers and makers of NKT17 cells.Experimental & molecular medicine · 2023
    Review
  9. Article
  10. Article
  11. METTL14-dependent mCell reports · 2022
    Article
  12. Article
  13. The impact of the gut microbiota on T cell ontogeny in the thymus.Cellular and molecular life sciences : CMLS · 2022
    Review
  14. Review
  15. Development of αβ T Cells with Innate Functions.Advances in experimental medicine and biology · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

49 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Vanja LazarevicDepartment of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
Alfred J Zullo
Michelle N Schweitzer
Tracy L Staton
Elena M Gallo
Gerald R Crabtree
Laurie H Glimcher
Harvard University · USHoward Hughes Medical Institute · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
The function of T Bet in EAEP01NS038037 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI WEINER, HOWARD L · 2000 to 2010
$12.8M
Signaling in T Lymphocyte DevelopmentR01AI060037 · NIAID · STANFORD UNIVERSITY · PI CRABTREE, GERALD R. · 2004 to 2010
$2.4M
NFAT Signaling and Down SyndromeR01HD055391 · NICHD · STANFORD UNIVERSITY · PI CRABTREE, GERALD R. · 2008 to 2012
$1.4M
NIAID NIH HHS R01 AI060037NIAID NIH HHS T32 AI007290NICHD NIH HHS R01 HD055391NINDS NIH HHS P01 NS038037NINDS NIH HHS P0NS038037PHS HHS UOAI31541
6 · The paper itself

Abstract

The influence of signals transmitted by the phosphatase calcineurin and the transcription factor NFAT on the development and function of natural killer T (NKT) cells is unclear. In this report, we demonstrate that the transcription factor early growth response 2 (Egr2), a target gene of NFAT, was specifically required for the ontogeny of NKT cells but not that of conventional CD4(+) or CD8(+) T cells. NKT cells developed normally in the absence of Egr1 or Egr3, which suggests that Egr2 is a specific regulator of NKT cell differentiation. We found that Egr2 was important in the selection, survival and maturation of NKT cells. Our findings emphasize the importance of the calcineurin-NFAT-Egr2 pathway in the development of the NKT lymphocyte lineage.

Indexed as

Cell DifferentiationAnimalsCalcineurinCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCells, CulturedEarly Growth Response Protein 2HumansMiceMice, Inbred C57BLMice, KnockoutNatural Killer T-CellsNFATC Transcription FactorsCalcineurinEarly Growth Response Protein 2Egr2 protein, mouseNFATC Transcription Factors

Identifiers

PMID19169262
PMCPMC2728767
OpenAlexW2004736287

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.