Evidence map›Paper›PMID 26678074›Full record

ArticleInflammation2016

The Golgi-Associated Plant Pathogenesis-Related Protein GAPR-1 Enhances Type I Interferon Signaling Pathway in Response to Toll-Like Receptor 4.

Qing Zhou, Lu Hao, Weiren Huang, Zhiming Cai

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. CAP superfamily proteins in human: a new target for cancer therapy.Medical oncology (Northwood, London, England) · 2024
    Review
  6. Article
  7. The Wheel of p53 Helps to Drive the Immune System.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Human microsporidian pathogenJournal of cell science · 2021
    Article
  10. Article
  11. Article
  12. Article
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

4 authors at 2 institutions in 1 country.

Qing ZhouKey Laboratory of Medical Reprogramming Technology, Shenzhen Second People's Hospital, First Affiliated Hospital of Shenzhen University, Shenzhen, 518039, China.
Lu HaoInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, 116044, China. haolu19860813@126.com.
Weiren HuangKey Laboratory of Medical Reprogramming Technology, Shenzhen Second People's Hospital, First Affiliated Hospital of Shenzhen University, Shenzhen, 518039, China. pony8980@163.com.
Zhiming CaiKey Laboratory of Medical Reprogramming Technology, Shenzhen Second People's Hospital, First Affiliated Hospital of Shenzhen University, Shenzhen, 518039, China. caizhiming2000@163.com.
Shenzhen Second People's Hospital · CNDalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipopolysaccharide (LPS) activates Toll-like receptor 4 (TLR4) through the TIRAP-MyD88 dependent and TRAM-TRIF dependent signaling pathways, respectively. However, the underlying relevance between two signaling pathways remains largely elusive. Here, we investigated the role of the Golgi-Associated plant Pathogenesis-Related protein (GAPR-1) in type I interferon (IFN) signaling pathway in response to TLR4. We found that TIRAP-MyD88 dependent kinase IRAK1 phosphorylated GAPR-1 at Serine 58 site. The phosphorylation of GAPR-1 promoted its interaction with TRAM-TRIF dependent inhibitor TMED7, and impaired TMED7-mediated disruption of the TRAM-TRIF complex to trigger IFN-β and the IL10 secretion. Collectively, our study identified a previously unrecognized role for GAPR-1 to control a unifying TLR4 signaling complex and to regulate type I IFN signaling activation. Understanding the mechanism of GAPR-1 in type I IFN signaling pathway would provide strategies for treatment of infectious diseases.

Indexed as

Adaptor Proteins, Vesicular TransportCell LineEnzyme ActivationHEK293 CellsHumansImmunity, InnateInterferon-betaInterleukin-10Interleukin-1 Receptor-Associated KinasesLipopolysaccharidesMembrane GlycoproteinsMembrane ProteinsMembrane Transport ProteinsMyeloid Differentiation Factor 88PhosphorylationReceptors, Interleukin-1Adaptor Proteins, Vesicular TransportGLIPR2 protein, humanIL10 protein, humanInterferon-betaInterleukin-10Interleukin-1 Receptor-Associated KinasesIRAK1 protein, humanLipopolysaccharidesMembrane GlycoproteinsMembrane ProteinsMembrane Transport ProteinsMYD88 protein, humanMyeloid Differentiation Factor 88Receptors, Interleukin-1TICAM1 protein, humanTIRAP protein, humanTLR4 protein, humanTMED7 protein, humanToll-Like Receptor 4TRAM1 protein, humanVesicular Transport ProteinsGAPR-1innate immunekinase phosphorylationtoll-like receptor 4type I IFN

Identifiers

PMID26678074
OpenAlexW2215370340

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.