Evidence map›Paper›PMID 26109639›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Cutting Edge: Synchronization of IRF1, JunB, and C/EBPβ Activities during TLR3-TLR7 Cross-Talk Orchestrates Timely Cytokine Synergy in the Proinflammatory Response.

Qian Liu, Yong Zhu, Wai Khang Yong, Newman Siu Kwan Sze, Nguan Soon Tan, Jeak Ling Ding

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 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
2.2field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Nanoparticle-MediatedACS nano · 2021
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Innate Control of Adaptive Immunity: Beyond the Three-Signal Paradigm.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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

6 authors at 2 institutions in 1 country.

Qian LiuDepartment of Biological Sciences, Faculty of Science, National University of Singapore, Singapore 117543; and.
Yong ZhuDepartment of Biological Sciences, Faculty of Science, National University of Singapore, Singapore 117543; and.
Wai Khang YongDepartment of Biological Sciences, Faculty of Science, National University of Singapore, Singapore 117543; and.
Newman Siu Kwan SzeSchool of Biological Sciences, Nanyang Technological University, Singapore 637511.
Nguan Soon TanSchool of Biological Sciences, Nanyang Technological University, Singapore 637511.
Jeak Ling DingDepartment of Biological Sciences, Faculty of Science, National University of Singapore, Singapore 117543; and dbsdjl@nus.edu.sg.
National University of Singapore · SGNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple pathogen-associated molecular pattern-induced TLR pathway cross-talk provokes proinflammatory cytokine synergy in macrophages, which is important for pathogen resistance and immune homeostasis. However, the detailed mechanisms are unclear. In this article, we demonstrate viral RNA analog-induced transcription synergy of Il6 and Il12b via IFN regulatory factor (IRF)1 (TLR3-TIR domain-containing adaptor inducing IFN-β [TRIF] responsive), C/EBPβ (TLR7-MyD88 responsive), and JunB (all responsive). Coactivation of the TLR3 and TLR7 pathways synchronizes the interaction of IRF1, JunB, and C/EBPβ with the Il6 and Il12b promoters, facilitating maximal gene expression. MyD88 pathway activation suppresses TRIF-induced IRF1 in a delayed manner, controlling the magnitude and timing of cytokine expression. Our findings provide novel mechanisms of cooperation of different TLR pathways to achieve optimal immune responses, with the potential for immunomodulatory strategies.

Indexed as

Activating Transcription Factor 6Adaptor Proteins, Vesicular TransportAnimalsCells, CulturedInflammationInterferon Regulatory Factor-1Interleukin-12 Subunit p40Interleukin-6MacrophagesMembrane GlycoproteinsMiceMyeloid Differentiation Factor 88Promoter Regions, GeneticReceptor Cross-TalkRNA, MessengerSignal TransductionActivating Transcription Factor 6Adaptor Proteins, Vesicular TransportAtf6b protein, mouseInterferon Regulatory Factor-1Interleukin-12 Subunit p40Interleukin-6Irf1 protein, mouseJunB protein, mouseMembrane GlycoproteinsMyd88 protein, mouseMyeloid Differentiation Factor 88RNA, MessengerTicam1 protein, mouseTLR3 protein, mouseTlr7 protein, mouseToll-Like Receptor 3Toll-Like Receptor 7Transcription Factors

Identifiers

PMID26109639
PMCPMC4505950
OpenAlexW1840371537

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.