Evidence map›Paper›PMID 26490636›Full record

ArticleMolecular immunology2015

Cell-autonomous requirement for TCF1 and LEF1 in the development of Natural Killer T cells.

Rosa Berga-Bolaños, Wandi S Zhu, Farrah C Steinke, Hai-Hui Xue, Jyoti Misra Sen

Abstract read
In one paragraph

Article in Molecular immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
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  7. TCF-1 Is Required for CD4 T Cell Persistence Functions during AlloImmunity.International journal of molecular sciences · 2023
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  12. Review
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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

5 authors.

Rosa Berga-BolañosImmune Cells and Inflammation Section, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States.
Wandi S ZhuImmune Cells and Inflammation Section, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States.
Farrah C SteinkeDepartment of Microbiology, Interdisciplinary Immunology Graduate Program, University of Iowa, Iowa City, IA 52242, United States.
Hai-Hui XueDepartment of Microbiology, Interdisciplinary Immunology Graduate Program, University of Iowa, Iowa City, IA 52242, United States.
Jyoti Misra SenImmune Cells and Inflammation Section, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, United States; Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States. Electronic address: Jyoti-Sen@nih.gov.

Funding

T cell development in the thymus and age-dependent thymic involutionZIAAG000768 · NIA · NATIONAL INSTITUTE ON AGING · PI EGAN, JOSEPHINE · 2009 to 2025
$4.0M
Signal Transduction in T cell development, function and agingZ01AG000768 · NIA · NATIONAL INSTITUTE ON AGING · PI SEN, JYOTI · 2004 to 2008
$1.5M
Intramural NIH HHS Z01 AG000768
6 · The paper itself

Abstract

Natural killer T (NKT) cells develop from common CD4(+) CD8(+) thymocyte precursors. Transcriptional programs that regulate the development of NKT cells in the thymus development remain to be fully delineated. Here, we demonstrate a cell-intrinsic requirement for transcription factors TCF1 and LEF1 for the development of all subsets of NKT cells. Conditional deletion of TCF1 alone results in a substantial reduction in NKT cells. The remaining NKT cells are eliminated when TCF1 and LEF1 are both deleted. These data reveal an essential role for TCF1 and LEF1 in development of NKT cells.

Indexed as

AnimalsCell DifferentiationHepatocyte Nuclear Factor 1-alphaLymphoid Enhancer-Binding Factor 1MiceMice, Inbred C57BLMice, KnockoutNatural Killer T-CellsThymocytesHepatocyte Nuclear Factor 1-alphaHnf1a protein, mouseLef1 protein, mouseLymphoid Enhancer-Binding Factor 1LEF1NKT cellsTCF1

Identifiers

PMID26490636
PMCPMC4636915

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Registered trials

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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.