Evidence map›Paper›PMID 26655903›Full record

ArticleCell reports2015

Inactivation of the Class II PI3K-C2β Potentiates Insulin Signaling and Sensitivity.

Samira Alliouachene, Benoit Bilanges, Gaëtan Chicanne, Karen E Anderson, Wayne Pearce, Khaled Ali, Colin Valet, York Posor, Pei Ching Low, Claire Chaussade and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Phosphoinositides as membrane organizers.Nature reviews. Molecular cell biology · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Phosphoinositide 3-Kinases as Potential Targets for Thrombosis Prevention.International journal of molecular sciences · 2022
    Review
  13. An Overview of Class II Phosphoinositide 3-Kinases.Current topics in microbiology and immunology · 2022
    Article
  14. PI3K Isoforms in B Cells.Current topics in microbiology and immunology · 2022
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Phosphatidylinositol 3-monophosphate: A novel actor in thrombopoiesis and thrombosis.Research and practice in thrombosis and haemostasis · 2020
    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

17 authors at 6 institutions in 3 countries.

Samira AlliouacheneUCL Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK. Electronic address: s.alliouachene@ucl.ac.uk.
Benoit BilangesUCL Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
Gaëtan ChicanneInserm/UPS UMR 1048, Institut des Maladies Métaboliques et Cardiovasculaires, 1 Avenue Jean Poulhès BP 84225, 31432 Toulouse Cedex 4, France.
Karen E AndersonInositide Laboratory, The Babraham Institute, Cambridge CB22 3AT, UK.
Wayne PearceUCL Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
Khaled AliUCL Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
Colin ValetInserm/UPS UMR 1048, Institut des Maladies Métaboliques et Cardiovasculaires, 1 Avenue Jean Poulhès BP 84225, 31432 Toulouse Cedex 4, France.
York PosorUCL Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
Pei Ching LowUCL Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
Claire ChaussadeUCL Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK.
Cheryl L ScudamoreMary Lyon Centre, MRC Harwell, Harwell Science and Innovation Campus, Harwell OX11 0RD, UK.
Rachel S SalamonDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Jonathan M BackerDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Len StephensInositide Laboratory, The Babraham Institute, Cambridge CB22 3AT, UK.
Phill T HawkinsInositide Laboratory, The Babraham Institute, Cambridge CB22 3AT, UK.
Bernard PayrastreInserm/UPS UMR 1048, Institut des Maladies Métaboliques et Cardiovasculaires, 1 Avenue Jean Poulhès BP 84225, 31432 Toulouse Cedex 4, France.
Bart VanhaesebroeckUCL Cancer Institute, University College London, 72 Huntley Street, London WC1E 6DD, UK. Electronic address: bart.vanh@ucl.ac.uk.
University College London · GBBabraham Institute · GBAlbert Einstein College of Medicine · USUniversité Toulouse III - Paul Sabatier · FRInstitut des Maladies Métaboliques et Cardiovasculaires · FRMary Lyon Centre at MRC Harwell · GB

Funding

Stable Isotope and Metabolomics CoreP60DK020541 · NIDDK · YESHIVA UNIVERSITY · PI PESSIN, JEFFREY E. · 1986 to 2014
$29.8M
Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Special Animal CoreP30DK041296 · NIDDK · YESHIVA UNIVERSITY · PI GUPTA, SANJEEV · 1989 to 2018
$22.9M
Biotechnology and Biological Sciences Research Council BB/I003916/1Biotechnology and Biological Sciences Research Council BB/I007806/1Biotechnology and Biological Sciences Research Council BB/J004456/1Biotechnology and Biological Sciences Research Council BBS/E/B/000C0413Biotechnology and Biological Sciences Research Council BBS/E/B/000C0415Cancer Research UK C23338/A15965Department of HealthMedical Research Council G0901338Medical Research Council MC_UP_1502/1NIDDK NIH HHS DK 20541NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P30 DK041296NIDDK NIH HHS P60 DK020541
6 · The paper itself

Abstract

In contrast to the class I phosphoinositide 3-kinases (PI3Ks), the organismal roles of the kinase activity of the class II PI3Ks are less clear. Here, we report that class II PI3K-C2β kinase-dead mice are viable and healthy but display an unanticipated enhanced insulin sensitivity and glucose tolerance, as well as protection against high-fat-diet-induced liver steatosis. Despite having a broad tissue distribution, systemic PI3K-C2β inhibition selectively enhances insulin signaling only in metabolic tissues. In a primary hepatocyte model, basal PI3P lipid levels are reduced by 60% upon PI3K-C2β inhibition. This results in an expansion of the very early APPL1-positive endosomal compartment and altered insulin receptor trafficking, correlating with an amplification of insulin-induced, class I PI3K-dependent Akt signaling, without impacting MAPK activity. These data reveal PI3K-C2β as a critical regulator of endosomal trafficking, specifically in insulin signaling, and identify PI3K-C2β as a potential drug target for insulin sensitization.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAutophagyBlood GlucoseCells, CulturedClass II Phosphatidylinositol 3-KinasesDiet, High-FatEndosomesFatty LiverGene Knock-In TechniquesHepatocytesInsulinLiverMiceMice, Inbred C57BLMitogen-Activated Protein KinasesAdaptor Proteins, Signal TransducingAppl1 protein, mouseBlood GlucoseClass II Phosphatidylinositol 3-KinasesInsulinMitogen-Activated Protein KinasesProto-Oncogene Proteins c-akt

Identifiers

PMID26655903
PMCPMC4675724
OpenAlexW2180533394

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.