Evidence map›Paper›PMID 15254086›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2004

Reanalysis of P2X7 receptor expression in rodent brain.

Joan A Sim, Mark T Young, Hye-Youn Sung, R Alan North, Annmarie Surprenant

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed
11.3field-weighted citation impact, top 1% 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

110 citing papers in PubMed, 262 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. P2XBrain, behavior, and immunity · 2023
    Article
  9. Animal Models for the Investigation of P2X7 Receptors.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Article
  12. Functional P2XThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. P2X7 Receptors Amplify CNS Damage in Neurodegenerative Diseases.International journal of molecular sciences · 2020
    Review
  17. Article
  18. The P2X7 Receptor: Central Hub of Brain Diseases.Frontiers in molecular neuroscience · 2020
    Review
  19. P2X7 Receptor Signaling in Stress and Depression.International journal of molecular sciences · 2019
    Review
  20. Review

50 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

5 authors at 4 institutions in 2 countries.

Joan A SimInstitute of Molecular Physiology, University of Sheffield, Western Bank, Sheffield S10 2TN, United Kingdom.
Mark T Young
Hye-Youn Sung
R Alan North
Annmarie Surprenant
University of Sheffield · GBProvidence College · USUniversity of Birmingham · GBUniversity of Manchester · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

P2X receptors are cationic-selective ion channels gated by extracellular ATP. There are seven subunits (P2X1-7), the first six of which are expressed throughout the peripheral and central nervous systems. P2X7 receptors are rapidly upregulated and activated as a result of inflammatory stimuli in immune cells, where they act not only as cationic channels but uniquely couple with rapid release of proinflammatory cytokines, cytoskeletal rearrangements, and apoptosis or necrotic cell death. The P2X7 receptor has been termed the cytolytic non-neuronal P2X receptor because it had not been detected in neurons until recently when it has been immunolocalized to several brain regions, particularly the hippocampus, and has been suggested to be involved in presynaptic modulation of transmitter release. Because its expression in brain neurons may have substantial functional implications, we have performed detailed immunocytochemical, immunoblot, and immunoprecipitation studies on brain and non-neuronal tissue using all currently available antibodies. We first examined rats, but staining patterns were inconsistent among antibodies; we therefore studied mice for which there are two P2X7 knock-out mice constructs available, one expressing the LacZ transgene. We found that P2X7 receptor protein is strongly and reliably detected in the submandibular gland and lung of wild-type mice but not in either of the P2X7-/- mice. However, we failed to find evidence for P2X7 receptor protein in hippocampal neurons or their input-output projections. Either the P2X7 protein in the hippocampus is below the limits of detection by the currently available methods or it is not present.

Indexed as

Brain ChemistryAnimalsAntibodies, MonoclonalCrosses, GeneticEpitopesHippocampusImmunoprecipitationLac OperonLungMaleMiceMice, Inbred C57BLMice, Inbred DBAMice, KnockoutNerve Tissue ProteinsNeuronsAntibodies, MonoclonalEpitopesNerve Tissue ProteinsP2rx7 protein, mouseReceptors, Purinergic P2Receptors, Purinergic P2X7

Identifiers

PMID15254086
PMCPMC6729549
OpenAlexW2131072721

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.