Evidence map›Paper›PMID 22499153›Full record

ArticleGlia2012

ATP signaling is deficient in cultured Pannexin1-null mouse astrocytes.

Sylvia O Suadicani, Rodolfo Iglesias, Junjie Wang, Gerhard Dahl, David C Spray, Eliana Scemes

Open access · greenAbstract read
In one paragraph

Article in Glia, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

92 citing papers in PubMed, 159 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Disease-relevant upregulation of P2YNature communications · 2024
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Pannexin1 channels in the liver: an open enemy.Frontiers in cell and developmental biology · 2023
    Review
  18. Article
  19. Review
  20. Review

32 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Sylvia O SuadicaniDominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Rodolfo Iglesias
Junjie Wang
Gerhard Dahl
David C Spray
Eliana Scemes
Albert Einstein College of Medicine · USUniversity of Miami · US

Funding

Project4: INTERACTION OF AUTOPHAGIC AND HETEROPHAGIC PATHWAYS IN LIVERP01DK041918 · NIDDK · YESHIVA UNIVERSITY · PI WOLKOFF, ALLAN W · 1990 to 2012
$19.1M
The Astrocyte Nexus: CX43-Protein InteractionsR01NS041282 · NINDS · YESHIVA UNIVERSITY · PI SPRAY, DAVID C · 2002 to 2011
$3.3M
Structural, Molecular, and Functional Specialization in Osteocyte MechanosensingR01AR057139 · NIAMS · CITY COLLEGE OF NEW YORK · PI SCHAFFLER, MITCHELL B, SPRAY, DAVID C · 2010 to 2014
$2.5M
Urothelial ATP Signaling and Diabetic Bladder DysfunctionR01DK081435 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SUADICANI, SYLVIA OTTILIE · 2009 to 2013
$1.7M
Mechanisms of ATP Release from Glial ProgenitorsR01NS052245 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SCEMES, ELIANA · 2007 to 2011
$1.6M
NIAMS NIH HHS R01 AR057139NIDDK NIH HHS P01 DK041918NIDDK NIH HHS R01 DK081435NINDS NIH HHS NS041282NINDS NIH HHS NS052245NINDS NIH HHS R01 NS041282NINDS NIH HHS R01 NS052245
6 · The paper itself

Abstract

Pannexins (Panx1, 2, and 3) comprise a group of proteins expressed in vertebrates that share weak yet significant sequence homology with the invertebrate gap junction proteins, the innexins. In contrast to the other vertebrate gap junction protein family (connexin), pannexins do not form intercellular channels, but at least Panx1 forms nonjunctional plasma membrane channels. Panx1 is ubiquitously expressed and has been shown to form large conductance (500 pS) channels that are voltage dependent, mechanosensitive, and permeable to relatively large molecules such as ATP. Pharmacological and knockdown approaches have indicated that Panx1 is the molecular substrate for the so-called "hemichannel" originally attributed to connexin43 and that Panx1 is the pore-forming unit of the P2X(7) receptor. Here, we describe, for the first time, conductance and permeability properties of Panx1-null astrocytes. The electrophysiological and fluorescence imaging analyses performed on these cells fully support our previous pharmacological and Panx1 knockdown studies that showed profoundly lower dye uptake and ATP release than wild-type untreated astrocytes. As a consequence of decreased ATP paracrine signaling, intercellular calcium wave spread is altered in Panx1-null astrocytes. Moreover, we found that in astrocytes as in Panx1-expressing oocytes, elevated extracellular K(+) activates Panx1 channels independently of membrane potential. Thus, on the basis of our present findings and our previous report, we propose that Panx1 channels serve as K(+) sensors for changes in the extracellular milieu such as those occurring under pathological conditions.

Indexed as

Adenosine TriphosphateAnimalsAstrocytesCalciumCalcium SignalingCells, CulturedConnexinsGap JunctionsMiceMice, KnockoutNerve Tissue ProteinsAdenosine TriphosphateCalciumConnexinsNerve Tissue ProteinsPanx1 protein, mouse

Identifiers

PMID22499153
PMCPMC3348971
OpenAlexW2081308255

What OpenQuestion holds

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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.