Evidence map›Paper›PMID 27697837›Full record

ArticleThe Journal of experimental medicine2016

NFATC3 promotes IRF7 transcriptional activity in plasmacy--toid dendritic cells.

Musheng Bao, York Wang, Ying Liu, Peiqing Shi, Hongbo Lu, Wenwen Sha, Leiyun Weng, Shino Hanabuchi, Jun Qin, Joel Plumas and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  5. Review
  6. Review
  7. Article
  8. Type I Interferon Production of Plasmacytoid Dendritic Cells under Control.International journal of molecular sciences · 2021
    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

13 authors at 4 institutions in 2 countries.

Musheng BaoBaylor Institute for Immunology Research, Dallas, TX 75204.ORCID 0000-0002-3567-6583
York WangBaylor Institute for Immunology Research, Dallas, TX 75204.ORCID 0000-0002-0077-0772
Ying LiuBaylor Institute for Immunology Research, Dallas, TX 75204.ORCID 0000-0002-6343-2498
Peiqing ShiBaylor Institute for Immunology Research, Dallas, TX 75204.ORCID 0000-0002-4526-7484
Hongbo LuBaylor Institute for Immunology Research, Dallas, TX 75204.
Wenwen ShaBaylor Institute for Immunology Research, Dallas, TX 75204.
Leiyun WengBaylor Institute for Immunology Research, Dallas, TX 75204.ORCID 0000-0003-2438-577X
Shino HanabuchiBaylor Institute for Immunology Research, Dallas, TX 75204.
Jun QinVerna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX 77030.
Joel PlumasEtablissement Français du Sang Rhone-Alpes, 38701 La Tronche, France.
Laurence ChaperotEtablissement Français du Sang Rhone-Alpes, 38701 La Tronche, France.ORCID 0000-0002-1479-9410
Zhiqiang ZhangImmunobiology and Transplant Research, Houston Methodist Research Institute, Houston, TX 77030.
Yong-Jun LiuBaylor Institute for Immunology Research, Dallas, TX 75204 yjliuanderson@yahoo.com.
Baylor University · USÉtablissement Français du Sang · FRBaylor College of Medicine · USHouston Methodist · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmacytoid dendritic cells (pDCs) rapidly produce large amounts of type 1 interferon (IFN) after Toll-like receptor 7 and 9 engagements. This specialized function of type 1 IFN production is directly linked to the constitutive expression of IRF7, the master transcription factor for type 1 IFN production. However, the IRF7 regulatory network in pDCs remains largely unknown. In this study, we identify that the transcription factor NFATC3 specifically binds to IRF7 and enhances IRF7-mediated IFN production. Furthermore, knockout of NFATC3 greatly reduced the CpG DNA-induced nuclear translocation of IRF7, which resulted in impaired type 1 IFN production in vitro and in vivo. In addition, we found that NFATC3 and IRF7 both bound to type 1 IFN promoters and that the NFAT binding site in IFN promoters was required for IRF7-mediated IFN expression. Collectively, our study shows that the transcription factor NFATC3 binds to IRF7 and functions synergistically to enhance IRF7-mediated IFN expression in pDCs.

Indexed as

Transcription, GeneticAnimalsBase SequenceCell NucleusCells, CulturedCRISPR-Cas SystemsDendritic CellsGene Knockdown TechniquesHEK293 CellsHumansInterferon Regulatory Factor-7Interferon Type IMiceNFATC Transcription FactorsOligodeoxyribonucleotidesPromoter Regions, GeneticCPG-oligonucleotideInterferon Regulatory Factor-7Interferon Type IIRF7 protein, humanIrf7 protein, mouseNFATC Transcription FactorsOligodeoxyribonucleotidestranscription factor NF-AT c3

Identifiers

PMID27697837
PMCPMC5068237
OpenAlexW2528722070

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.