Evidence map›Paper›PMID 28740220›Full record

ArticleScientific reports2017

The Tnfaip8-PE complex is a novel upstream effector in the anti-autophagic action of insulin.

Ji-Soo Kim, Jimin Park, Mi-Sun Kim, Ji-Young Ha, Ye-Won Jang, Dong Hae Shin, Jin H Son

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. TNFAIP8: Inflammation, Immunity and Human Diseases.Journal of cellular immunology · 2019
    Article
  10. Article
  11. Review
  12. Article
  13. TIPE Family of Proteins and Its Implications in Different Chronic Diseases.International journal of molecular sciences · 2018
    Review
  14. 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

7 authors at 1 institution in 1 country.

Ji-Soo KimCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Global Top5 Research Program, Ewha W. University, Seoul, 03760, Republic of Korea.
Jimin ParkCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Global Top5 Research Program, Ewha W. University, Seoul, 03760, Republic of Korea.
Mi-Sun KimCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Global Top5 Research Program, Ewha W. University, Seoul, 03760, Republic of Korea.
Ji-Young HaCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Global Top5 Research Program, Ewha W. University, Seoul, 03760, Republic of Korea.
Ye-Won JangCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Global Top5 Research Program, Ewha W. University, Seoul, 03760, Republic of Korea.
Dong Hae ShinCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Global Top5 Research Program, Ewha W. University, Seoul, 03760, Republic of Korea. dhshin55@ewha.ac.kr.
Jin H SonCollege of Pharmacy and Graduate School of Pharmaceutical Sciences, Global Top5 Research Program, Ewha W. University, Seoul, 03760, Republic of Korea. hjson@ewha.ac.kr.
Ewha Womans University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defective hepatic autophagy is observed in obesity and diabetes, whereas autophagy is inhibited by insulin in hepatocytes. Insulin-induced anti-autophagy is mediated by non-canonical Gαi3 signaling via an unknown mechanism. Previously, we identified the anti-autophagic activity of Tnfaip8 via activation of mammalian target of rapamycin (mTOR) in the nervous system. Here, we demonstrate that insulin temporally induces Tnfaip8, which mediates the anti-autophagic action of insulin through formation of a novel ternary complex including Tnfaip8, phosphatidylethanolamine (PE) and Gαi3. Specifically, an X-ray crystallographic study of Tnfaip8 from Mus musculus (mTnfaip8) at 2.03 Å together with LC-MS analyses reveals PE in the hydrophobic cavity. However, an mTnfaip8 mutant lacking PE does not interact with Gαi3, indicating that the PE component is critical for the anti-autophagic action of mTnfaip8 via interaction with Gαi3. Therefore, the mTnfaip8-PE complex may act as an essential upstream effector via ternary complex formation most likely with active Gαi3 during insulin-induced anti-autophagy.

Indexed as

AutophagyAmino Acid SequenceAnimalsApoptosis Regulatory ProteinsCrystallography, X-RayGTP-Binding Protein alpha Subunits, Gi-GoInsulinMicePhosphatidylethanolaminesProtein BindingProtein ConformationSequence HomologyApoptosis Regulatory ProteinsGTP-Binding Protein alpha Subunits, Gi-GoInsulinphosphatidylethanolaminePhosphatidylethanolaminesTNFAIP8 protein, mouse

Identifiers

PMID28740220
PMCPMC5524748
OpenAlexW2736494644

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.