Evidence map›Paper›PMID 26413467›Full record

ArticleMolecular metabolism2015

Pannexin 1 is required for full activation of insulin-stimulated glucose uptake in adipocytes.

Samantha E Adamson, Akshaya K Meher, Yu-Hsin Chiu, Joanna K Sandilos, Nathaniel P Oberholtzer, Natalie N Walker, Stefan R Hargett, Scott A Seaman, Shayn M Peirce-Cottler, Brant E Isakson and 5 more

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

46 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
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  6. Adipose tissue releases nucleosides.American journal of physiology. Cell physiology · 2026
    Article
  7. Article
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  9. Novel Naphthyridones Targeting Pannexin 1 for Colitis Management.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

15 authors at 1 institution in 1 country.

Samantha E AdamsonDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA ; Cardiovascular Research Center, University of Virginia, Charlottesville, VA 22908, USA.
Akshaya K MeherDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA.
Yu-Hsin ChiuDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA.
Joanna K SandilosDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA.
Nathaniel P OberholtzerDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA.
Natalie N WalkerDepartment of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Stefan R HargettDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA 22908, USA.
Scott A SeamanCardiovascular Research Center, University of Virginia, Charlottesville, VA 22908, USA ; Department of Biomedical Engineering, University of Virginia, Charlottesville, VA 22908, USA.
Shayn M Peirce-CottlerCardiovascular Research Center, University of Virginia, Charlottesville, VA 22908, USA ; Department of Biomedical Engineering, University of Virginia, Charlottesville, VA 22908, USA.
Brant E IsaksonCardiovascular Research Center, University of Virginia, Charlottesville, VA 22908, USA ; Department of Physiology, University of Virginia, Charlottesville, VA 22908, USA.
Coleen A McNamaraCardiovascular Research Center, University of Virginia, Charlottesville, VA 22908, USA ; Department of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Susanna R KellerDepartment of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Thurl E HarrisDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA.
Douglas A BaylissDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA.
Norbert LeitingerDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA ; Cardiovascular Research Center, University of Virginia, Charlottesville, VA 22908, USA.
University of Virginia · US

Funding

Role of Pannexins in Vascular Smooth Muscle CellsP01HL120840 · NHLBI · UNIVERSITY OF VIRGINIA · PI BAYLISS, DOUGLAS A., RAVICHANDRAN, KODI S · 2014 to 2023
$24.0M
BASIC CARDIOVASCULAR RESEARCH TRAINING GRANTT32HL007284 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Brant E Isakson, Gary K Owens · 1985 to 2026
$19.6M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007267 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GARCIA-BLANCO, MARIANO A. · 1985 to 2024
$13.4M
BIOTECHNOLOGY TRAINING PROGRAMT32GM008715 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LAURIE, GORDON WILLIAM · 2000 to 2019
$6.6M
Mechanisms of Heterocellular Signaling at the Myoenothelial JunctionR01HL088554 · NHLBI · UNIVERSITY OF VIRGINIA · PI ISAKSON, BRANT E, WEISS, MITCHELL J · 2008 to 2017
$3.8M
Role of Oxidized neutral lipids in adipocyte functionR01DK101946 · NIDDK · UNIVERSITY OF VIRGINIA · PI HARRIS, THURL E. · 2014 to 2018
$1.7M
Becton Dickinson LSR IIS10RR025460 · NCRR · UNIVERSITY OF VIRGINIA · PI BENDER, TIMOTHY P. · 2009 to 2009
$379k
NCRR NIH HHS S10 RR025460NHLBI NIH HHS P01 HL120840NHLBI NIH HHS R01 HL088554NHLBI NIH HHS T32 HL007284NIDDK NIH HHS R01 DK101946NIGMS NIH HHS T32 GM007267NIGMS NIH HHS T32 GM008715
6 · The paper itself

Abstract

objectiveDefective glucose uptake in adipocytes leads to impaired metabolic homeostasis and insulin resistance, hallmarks of type 2 diabetes. Extracellular ATP-derived nucleotides and nucleosides are important regulators of adipocyte function, but the pathway for controlled ATP release from adipocytes is unknown. Here, we investigated whether Pannexin 1 (Panx1) channels control ATP release from adipocytes and contribute to metabolic homeostasis.

methodsWe assessed Panx1 functionality in cultured 3T3-L1 adipocytes and in adipocytes isolated from murine white adipose tissue by measuring ATP release in response to known activators of Panx1 channels. Glucose uptake in cultured 3T3-L1 adipocytes was measured in the presence of Panx1 pharmacologic inhibitors and in adipocytes isolated from white adipose tissue from wildtype (WT) or adipocyte-specific Panx1 knockout (AdipPanx1 KO) mice generated in our laboratory. We performed in vivo glucose uptake studies in chow fed WT and AdipPanx1 KO mice and assessed insulin resistance in WT and AdipPanx1 KO mice fed a high fat diet for 12 weeks. Panx1 channel function was assessed in response to insulin by performing electrophysiologic recordings in a heterologous expression system. Finally, we measured Panx1 mRNA in human visceral adipose tissue samples by qRT-PCR and compared expression levels with glucose levels and HOMA-IR measurements in patients.

resultsOur data show that adipocytes express functional Pannexin 1 (Panx1) channels that can be activated to release ATP. Pharmacologic inhibition or selective genetic deletion of Panx1 from adipocytes decreased insulin-induced glucose uptake in vitro and in vivo and exacerbated diet-induced insulin resistance in mice. Further, we identify insulin as a novel activator of Panx1 channels. In obese humans Panx1 expression in adipose tissue is increased and correlates with the degree of insulin resistance.

conclusionsWe show that Panx1 channel activity regulates insulin-stimulated glucose uptake in adipocytes and thus contributes to control of metabolic homeostasis.

Indexed as

AdipocyteExtracellular ATPGlucose uptakePannexin 1

Identifiers

PMID26413467
PMCPMC4563021
OpenAlexW2128291544

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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.