Evidence map›Paper›PMID 10960067›Full record

ArticleBritish journal of pharmacology2000

Study of A(2A) adenosine receptor gene deficient mice reveals that adenosine analogue CGS 21680 possesses no A(2A) receptor-unrelated lymphotoxicity.

S G Apasov, J F Chen, P T Smith, M A Schwarzschild, J S Fink, M V Sitkovsky

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 31 citations in OpenAlex.

  1. Remote control of movement disorders using a photoactive adenosine AJournal of controlled release : official journal of the Controlled Release Society · 2018
    Article
  2. Immune Alterations in CD8Molecular neurobiology · 2018
    Article
  3. Review
  4. Article
  5. Article
  6. Purinergic signalling and immune cells.Purinergic signalling · 2014
    Review
  7. Article
  8. Adenosine A2A receptor activation protects CD4+ T lymphocytes against activation-induced cell death.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    Article
  9. Article
  10. A2A adenosine receptor protects tumors from antitumor T cells.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  11. Article
  12. 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

6 authors at 2 institutions in 1 country.

S G ApasovLaboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, MD 20892-1892, USA.
J F Chen
P T Smith
M A Schwarzschild
J S Fink
M V Sitkovsky
Massachusetts General Hospital · USNational Institute of Allergy and Infectious Diseases · US

Funding

ADENOSINE A2 RECEPTORS AND PSYCHOSTIMULANT INTERACTIONSR01DA007496 · NIDA · MASSACHUSETTS GENERAL HOSPITAL · PI SCHWARZSCHILD, MICHAEL A · 1992 to 1999
–
PURINERGIC REGULATION OF IMMUNE RESPONSEZ01AI000626 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI SITKOVSKY, MICHAIL · 1992 to 2003
–
NIDA NIH HHS DA07496
6 · The paper itself

Abstract

Cell surface A(2A) adenosine receptor (A(2A)R) mediated signalling affects a variety of important processes and adenosine analogues possess promising pharmacological properties. Demonstrating the receptor specificity of potentially lymphotoxic adenosine-based drugs facilitates their development for clinical applications. To distinguish between the receptor-dependent and -independent lymphotoxicity and apoptotic activity of adenosine and its analogues we used lymphocytes from A(2A)R-deficient mice. Comparison of A(2A)R-expressing (+/+) and A(2A)R-deficient (-/-) cells in cyclic AMP accumulation assays confirmed that the A(2A)R agonist CGS 21680 is indeed selective for A(2A) receptors in T-lymphocytes. Incubation of A(2A)R-expressing thymocytes with extracellular adenosine or CGS 21680 in vitro results in the death of about 7-15% of thymocytes. In contrast, no death was induced in parallel assays in cells from A(2A)R-deficient mice, providing genetic evidence that CGS 21680 does not display adenosine receptor-independent intracellular cytotoxicity. The A(2A) receptor-specific lymphotoxicity of CGS 21680 is also demonstrated in a long-term (6-day) in vitro model of thymocyte positive selection where addition of A(2A)R antagonist ZM 241,385 did block the effects of CGS 21680, allowing the survival of T cells. The use of cells from adenosine receptor-deficient animals is proposed as a part of the screening process for potential adenosine-based drugs for their receptor-independent cytotoxicity and lymphotoxicity.

Indexed as

AdenosineAnimalsApoptosisCell SurvivalCyclic AMPMicePhenethylaminesReceptors, Antigen, T-CellReceptors, Purinergic P1T-Lymphocytes2-(4-(2-carboxyethyl)phenethylamino)-5'-N-ethylcarboxamidoadenosineAdenosineCyclic AMPPhenethylaminesReceptors, Antigen, T-CellReceptors, Purinergic P1

Identifiers

PMID10960067
PMCPMC1572291
OpenAlexW2071368114

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.