Evidence map›Paper›PMID 24419036›Full record

ReviewChannels (Austin, Tex.)2014

Intrinsic properties and regulation of Pannexin 1 channel.

Yu-Hsin Chiu, Kodi S Ravichandran, Douglas A Bayliss

Abstract 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 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Gap Junctions in Ctenophora.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  9. Article
  10. Role of ATP in migraine mechanisms: focus on P2X3 receptors.The journal of headache and pain · 2023
    Review
  11. Article
  12. Endogenous pannexin1 channels form functional intercellular cell-cell channels with characteristic voltage-dependent properties.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Pannexin1 channels-a potential therapeutic target in inflammation.Frontiers in cell and developmental biology · 2022
    Review
  14. On the molecular nature of large-pore channels.Journal of molecular biology · 2021
    Review
  15. Article
  16. Review
  17. Pannexin 1 Transgenic Mice: Human Diseases and Sleep-Wake Function Revision.International journal of molecular sciences · 2021
    Article
  18. Article
  19. Article
  20. Article
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

3 authors.

Yu-Hsin ChiuDepartment of Pharmacology; University of Virginia; Charlottesville, VA USA.
Kodi S RavichandranBeirne B. Carter Center for Immunology Research; University of Virginia; Charlottesville, VA USA; Center for Cell Clearance; University of Virginia; Charlottesville, VA USA; Department of Microbiology; Immunology and Cancer Research; University of Virginia; Charlottesville, VA USA.
Douglas A BaylissDepartment of Pharmacology; University of Virginia; Charlottesville, VA USA.

Funding

Role of ELMO and DOCK 180 in signaling to engulfmentR01GM064709 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LORENZ, ULRIKE, RAVICHANDRAN, KODI S · 2003 to 2016
$3.6M
Molecular Bases for Motoneuronal NeuromodulationR01NS033583 · NINDS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BAYLISS, DOUGLAS A. · 2001 to 2011
$3.2M
Release of find-me signals during apoptotic cell clearanceR01GM107848 · NIGMS · UNIVERSITY OF VIRGINIA · PI BAYLISS, DOUGLAS A., RAVICHANDRAN, KODI S · 2013 to 2016
$1.2M
DEVELOPMENT OF BRAINSTEM NEUROTRANSMITTER SYSTEMSR29NS033583 · NINDS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BAYLISS, DOUGLAS A · 1995 to 1999
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NIGMS NIH HHS GM064709NIGMS NIH HHS GM107848NIGMS NIH HHS R01 GM064709NIGMS NIH HHS R01 GM107848NINDS NIH HHS NS033583NINDS NIH HHS R01 NS033583NINDS NIH HHS R29 NS033583
6 · The paper itself

Abstract

Pannexin 1 (Panx1) channels are generally represented as non-selective, large-pore channels that release ATP. Emerging roles have been described for Panx1 in mediating purinergic signaling in the normal nervous, cardiovascular, and immune systems, where they may be activated by mechanical stress, ionotropic and metabotropic receptor signaling, and via proteolytic cleavage of the Panx1 C-terminus. Panx1 channels are widely expressed in various cell types, and it is now thought that targeting these channels therapeutically may be beneficial in a number of pathophysiological contexts, such as asthma, atherosclerosis, hypertension, and ischemic-induced seizures. Even as interest in Panx1 channels is burgeoning, some of their basic properties, mechanisms of modulation, and proposed functions remain controversial, with recent reports challenging some long-held views regarding Panx1 channels. In this brief review, we summarize some well-established features of Panx1 channels; we then address some current confounding issues surrounding Panx1 channels, especially with respect to intrinsic channel properties, in order to raise awareness of these unsettled issues for future research.

Indexed as

Adenosine TriphosphateConnexinsHumansNerve Tissue ProteinsProtein Structure, TertiaryReceptors, Purinergic P2XSignal TransductionAdenosine TriphosphateConnexinsNerve Tissue ProteinsPANX1 protein, humanReceptors, Purinergic P2XATP releaseionic selectivityP2X receptorPannexin 1unitary conductance

Identifiers

PMID24419036
PMCPMC4048298

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.