Evidence map›Paper›PMID 24576994›Full record

ReviewChannels (Austin, Tex.)2014

Pannexin-1 as a potentiator of ligand-gated receptor signaling.

Brant E Isakson, Roger J Thompson

Open access · goldAbstract readReview
In one paragraph

Review in Channels (Austin, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Pharmacology of pannexin channels.Current opinion in pharmacology · 2023
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. P2X7 Interactions and Signaling - Making Head or Tail of It.Frontiers in molecular neuroscience · 2019
    Review
  11. Article
  12. Article
  13. Therapeutic strategies targeting connexins.Nature reviews. Drug discovery · 2018
    Review
  14. Pannexin-1 channels on endothelial cells mediate vascular inflammation during lung ischemia-reperfusion injury.American journal of physiology. Lung cellular and molecular physiology · 2018
    Article
  15. Connexins and Pannexins in Vascular Function and Disease.International journal of molecular sciences · 2018
    Review
  16. Potential role for a specialized βJournal of orthopaedic research : official publication of the Orthopaedic Research Society · 2018
    Article
  17. Review
  18. Article
  19. Article
  20. Independent origins of neurons and synapses: insights from ctenophores.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    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

2 authors at 2 institutions in 3 countries.

Brant E IsaksonRobert M. Berne Cardiovascular Research Center; University of Virginia School of Medicine; Charlottesville, VA USA; Department of Molecular Physiology and Biophysics; University of Virginia School of Medicine; Charlottesville, VA USA.
Roger J ThompsonHotchkiss Brain Institute; Department of Cell Biology and Anatomy; University of Calgary; Calgary, AB Canada.
Allen Institute for Brain Science · USCharlottesville Medical Research · US

Funding

Mechanisms of Heterocellular Signaling at the Myoenothelial JunctionR01HL088554 · NHLBI · UNIVERSITY OF VIRGINIA · PI ISAKSON, BRANT E, WEISS, MITCHELL J · 2008 to 2017
$3.8M
Mechanism of PAI-1 Polarization to Myoendothelial JunctionsR21HL107963 · NHLBI · UNIVERSITY OF VIRGINIA · PI ISAKSON, BRANT E · 2012 to 2013
$414k
NHLBI NIH HHS HL088554NHLBI NIH HHS HL107963NHLBI NIH HHS R01 HL088554NHLBI NIH HHS R21 HL107963
6 · The paper itself

Abstract

Pannexins are a class of plasma membrane spanning proteins that presumably form a hexameric, non-selective ion channel. Although similar in secondary structure to the connexins, pannexins notably do not form endogenous gap junctions and act as bona fide ion channels. The pannexins have been primarily studied as ATP-release channels, but the overall diversity of their functions is still being elucidated. There is an intriguing theme with pannexins that has begun to develop. In this review we analyze several recent reports that converge on the idea that pannexin channels (namely Panx1) can potentiate ligand-gated receptor signaling. Although the literature remains sparse, this emerging concept appears consistent between both ionotropic and metabotropic receptors of several ligand families.

Indexed as

Adenosine TriphosphateConnexinsHumansLigandsNerve Tissue ProteinsNeuronsReceptors, AdrenergicReceptors, BradykininReceptors, HistamineReceptors, N-Methyl-D-AspartateReceptors, Purinergic P2X7Receptors, ThrombinSignal TransductionAdenosine TriphosphateConnexinsLigandsNerve Tissue ProteinsPANX1 protein, humanReceptors, AdrenergicReceptors, BradykininReceptors, HistamineReceptors, N-Methyl-D-AspartateReceptors, Purinergic P2X7Receptors, Thrombinadrenergic receptoralpha1Rgap junctionG-protein coupled receptorhemichannelionotropic receptorNMDA receptorpannexinpurinergic

Identifiers

PMID24576994
PMCPMC4048300
OpenAlexW2088569604

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.