Evidence map›Paper›PMID 22987361›Full record

ArticlePurinergic signalling2013

Endothelial P2X7 receptors' expression is reduced by schistosomiasis.

Suellen D'Arc Dos Santos Oliveira, Robson Coutinho-Silva, Claudia Lucia Martins Silva

Open access · bronzeAbstract read
In one paragraph

Article in Purinergic signalling, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Endothelial c-IAP2 loss amplifies P2X7 receptor-driven inflammation and worsens schistosomiasis-associated pulmonary hypertension.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Review
  3. Altered purinergic P2X7 and ABiomedical journal · 2024
    Article
  4. P2YFrontiers in immunology · 2023
    Article
  5. Review
  6. Review
  7. Review
  8. P2RX7 at the Host-Pathogen Interface of Infectious Diseases.Microbiology and molecular biology reviews : MMBR · 2021
    Review
  9. Review
  10. P2X7 Receptors: An Untapped Target for the Management of Cardiovascular Disease.Arteriosclerosis, thrombosis, and vascular biology · 2021
    Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. 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 at 2 institutions in 1 country.

Suellen D'Arc Dos Santos OliveiraInstituto de Ciências Biomédicas, Laboratory of Biochemical and Molecular Pharmacology, Universidade Federal do Rio de Janeiro, Av. Carlos Chagas Filho, 373, CCS, room J-17, Cidade Universitária, Rio de Janeiro, 21941-599, Brazil.
Robson Coutinho-Silva
Claudia Lucia Martins Silva
Universidade Federal do Rio de Janeiro · BRNational Council for Scientific and Technological Development · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial cells control vascular tone, permeability and leukocyte transmigration and are modulated by pro-inflammatory mediators. Schistosomiasis is an intravascular disease associated with inflammation, therefore altering endothelial cells' phenotype. Purinergic P2X7 receptors (P2X7R) play an important role in inflammation; however, the impact of the disease upon endothelial P2X7R function or expression has not been explored. Using ethidium bromide uptake to investigate P2X7R function, we observed that the effects of ATP (3 mM) and the P2X7R agonist 3'-O-(4-benzoyl)-ATP (BzATP) were smaller in mesenteric endothelial cells from the Schistosoma mansoni-infected group than in the control group. In the control group, BzATP induced endothelial nitric oxide production, which was blocked by the P2X7R antagonists KN-62 and A740003. However, in the infected group, we observed a reduced effect of BzATP and no effect of both P2X7R antagonists, suggesting a downregulation of endothelial P2X7R in schistosomiasis. We observed similar results in both infected and P2X7R(-/-) groups, which were also comparable to data obtained with KN-62- or A740004-treated control cells. Data from Western blot and immunocytochemistry assays confirmed the reduced expression of P2X7R in the infected group. In conclusion, our data show a downregulation of P2X7R in schistosomiasis infection, which likely limits the infection-related endothelial damage.

Indexed as

Adenosine TriphosphateAnimalsBlotting, WesternCell Membrane PermeabilityCells, CulturedData Interpretation, StatisticalEndothelium, VascularFluorescent DyesImmunohistochemistryMaleMiceMice, Inbred C57BLNitric OxideReceptors, Purinergic P2X7Schistosomiasis mansoni3'-O-(4-benzoyl)benzoyladenosine 5'-triphosphateAdenosine TriphosphateFluorescent DyesNitric OxideReceptors, Purinergic P2X7

Identifiers

PMID22987361
PMCPMC3568429
OpenAlexW1994793091

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.