Evidence map›Paper›PMID 29133412›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Cell-autonomous adiposity through increased cell surface GLUT4 due to ankyrin-B deficiency.

Damaris N Lorenzo, Vann Bennett

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

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  12. Frontiers in oncology · 2021
    Article
  13. Review
  14. Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  15. Obesity: Ankyrin-B in susceptibility to obesity.Nature reviews. Endocrinology · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Damaris N LorenzoHoward Hughes Medical Institute, Duke University, Durham, NC 27710; dlorenzo@email.unc.edu benne012@mc.duke.edu.ORCID 0000-0002-6856-2988
Vann BennettHoward Hughes Medical Institute, Duke University, Durham, NC 27710; dlorenzo@email.unc.edu benne012@mc.duke.edu.
Howard Hughes Medical Institute · US

Funding

UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Ian Michael Carroll · 1999 to 2026
$31.6M
Howard Hughes Medical InstituteNIDDK NIH HHS P30 DK056350
6 · The paper itself

Abstract

Obesity typically is linked to caloric imbalance as a result of overnutrition. Here we propose a cell-autonomous mechanism for adiposity as a result of persistent cell surface glucose transporter type 4 (GLUT4) in adipocytes resulting from impaired function of ankyrin-B (AnkB) in coupling GLUT4 to clathrin-mediated endocytosis. Adipose tissue-specific AnkB-KO mice develop obesity and progressive pancreatic islet dysfunction with age or high-fat diet (HFD). AnkB-deficient adipocytes exhibit increased lipid accumulation associated with increased glucose uptake and impaired endocytosis of GLUT4. AnkB binds directly to GLUT4 and clathrin and promotes their association in adipocytes. AnkB variants that fail to restore normal lipid accumulation and GLUT4 localization in adipocytes are present in 1.3% of European Americans and 8.4% of African Americans, and are candidates to contribute to obesity susceptibility in humans.

Indexed as

AdipocytesAdiposityAnimalsAnkyrinsBiological TransportBlack or African AmericanBlack PeopleClathrinDiet, High-FatEndocytosisGene Expression RegulationGlucoseGlucose Transporter Type 4HumansIslets of LangerhansMaleAnk2 protein, mouseAnkyrinsClathrinGlucoseGlucose Transporter Type 4Slc2a4 protein, mouseankyrin-BclathrinGlut4membrane transportobesity

Identifiers

PMID29133412
PMCPMC5715754
OpenAlexW2770620441

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.