Evidence map›Paper›PMID 24227775›Full record

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

Batf3 and Id2 have a synergistic effect on Irf8-directed classical CD8α+ dendritic cell development.

Hemant Jaiswal, Monika Kaushik, Rachid Sougrat, Monica Gupta, Anup Dey, Rohit Verma, Keiko Ozato, Prafullakumar Tailor

Open access · greenAbstract 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 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Mutation inFrontiers in immunology · 2021
    Article
  12. Article
  13. Cell-autonomous FLT3L shedding via ADAM10 mediates conventional dendritic cell development in mouse spleen.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  14. Article
  15. Article
  16. Regulation of myelopoiesis by the transcription factor IRF8.International journal of hematology · 2015
    Review
  17. Article
  18. Article
  19. Review
  20. Dendritic cell-targeted vaccines.Frontiers in immunology · 2014
    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 at 3 institutions in 3 countries.

Hemant JaiswalLaboratory of Innate Immunity, National Institute of Immunology, New Delhi 110067, India;
Monika Kaushik
Rachid Sougrat
Monica Gupta
Anup Dey
Rohit Verma
Keiko Ozato
Prafullakumar Tailor
National Institute of Immunology · INNational Institutes of Health · USKing Abdullah University of Science and Technology · SA

Funding

Gene Regulation In The Immune SystemZIAHD001310 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI OZATO, KEIKO · 2009 to 2025
$15.0M
Intramural NIH HHS Z99 HD999999
6 · The paper itself

Abstract

Dendritic cells (DCs) are heterogeneous cell populations represented by different subtypes, each varying in terms of gene expression patterns and specific functions. Recent studies identified transcription factors essential for the development of different DC subtypes, yet molecular mechanisms for the developmental program and functions remain poorly understood. In this study, we developed and characterized a mouse DC progenitor-like cell line, designated DC9, from Irf8(-/-) bone marrow cells as a model for DC development and function. Expression of Irf8 in DC9 cells led to plasmacytoid DCs and CD8α(+) DC-like cells, with a concomitant increase in plasmacytoid DC- and CD8α(+) DC-specific gene transcripts and induction of type I IFNs and IL12p40 following TLR ligand stimulation. Irf8 expression in DC9 cells led to an increase in Id2 and Batf3 transcript levels, transcription factors shown to be important for the development of CD8α(+) DCs. We show that, without Irf8, expression of Id2 and Batf3 was not sufficient for directing classical CD8α(+) DC development. When coexpressed with Irf8, Batf3 and Id2 had a synergistic effect on classical CD8α(+) DC development. We demonstrate that Irf8 is upstream of Batf3 and Id2 in the classical CD8α(+) DC developmental program and define the hierarchical relationship of transcription factors important for classical CD8α(+) DC development.

Indexed as

AnimalsBasic-Leucine Zipper Transcription FactorsCD8 AntigensCell DifferentiationCell LineDendritesDendritic CellsGene Expression RegulationHematopoietic Stem CellsInhibitor of Differentiation Protein 2Interferon-alphaInterferon Regulatory Factor-8Interferon Regulatory FactorsInterleukin-12 Subunit p40Membrane ProteinsMiceBasic-Leucine Zipper Transcription FactorsCD8 antigen, alpha chainCD8 Antigensflt3 ligand proteinIdb2 protein, mouseInhibitor of Differentiation Protein 2Interferon-alphaInterferon Regulatory Factor-8Interferon Regulatory FactorsInterleukin-12 Subunit p40Membrane ProteinsRecombinant Fusion ProteinsRepressor ProteinsRNA, MessengerSNFT protein, mouse

Identifiers

PMID24227775
PMCPMC4805111
OpenAlexW2140066353

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.