Evidence map›Paper›PMID 16025270›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2005

Evidence for the existence of P2Y1,2,4 receptor subtypes in HEK-293 cells: reactivation of P2Y1 receptors after repetitive agonist application.

Wolfgang Fischer, Heike Franke, Helke Gröger-Arndt, Peter Illes

Abstract read
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In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 24% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  3. Genetically-encoded BRET probes shed light on ligand bias-induced variable ion selectivity in TRPV1 and P2X5/7.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  14. G-protein-mediated inhibition of the Trp channel TRPM1 requires the Gβγ dimer.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  15. Cation-pi interaction regulates ligand-binding affinity and signaling of integrin alpha4beta7.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  16. Echinacea-induced cytosolic Ca2+ elevation in HEK293.BMC complementary and alternative medicine · 2010
    Article
  17. Animal cells connected by nanotubes can be electrically coupled through interposed gap-junction channels.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  18. Article
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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

4 authors at 1 institution in 1 country.

Wolfgang FischerRudolf-Boehm-Institut für Pharmakologie und Toxikologie, Universität Leipzig, Haertelstrasse 16-18, 04107 Leipzig, Germany. Wolfgang.Fischer@medizin.uni-leipzig.de
Heike Franke
Helke Gröger-Arndt
Peter Illes
Leipzig University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ATP, ADPbetaS and UTP induced a comparable rise in the intracellular Ca2+ concentration ([Ca2+]i) in HEK-293 cells using fura-2 microfluorimetry. The responses persisted in Ca2+-free medium, but were abolished following depletion of intracellular Ca2+ stores by cyclopiazonic acid. Cross-desensitisation experiments demonstrated that exposure to ADPbetaS has no marked effect on UTP-induced [Ca2+]i transients and vice versa. Whereas the P2Y1 receptor-selective antagonist 2'-deoxy-N6-methyladenosine 3',5'-diphosphate (MRS 2179) abolished the responses to ADPbetaS, it decreased and did not alter the responses to ATP and UTP respectively. Although the P2Y1/P2Y4 receptor-preferential antagonist pyridoxalphosphate-6-azophenyl-2',4'-disulphonic acid (PPADS) abolished the responses to ADPbetaS, and decreased those to ATP, it also depressed the UTP-induced [Ca2+]i transients. Suramin, an antagonist with preference for P2Y2 receptors decreased both the ATP- and UTP-induced [Ca2+]i reactions. After numerous splittings, HEK-293 cells failed to react to ADPbetaS; however, repeated superfusion with this P2Y1 receptor agonist restored the [Ca2+]i signals. In agreement with the functional data, real-time polymerase chain reaction and immunocytochemical studies indicated the presence of P2Y1, P2Y2 and P2Y4 receptors. Our findings raise doubt with respect to the reliability of HEK-293 cells as expression systems for recombinant P2X receptors, because of a possible functional interaction with endogenous P2Y receptors.

Indexed as

Adenosine TriphosphateCalcium SignalingCell LineChelating AgentsFluorescent DyesFura-2Gene ExpressionHumansPurinergic P2 Receptor AgonistsReceptors, Purinergic P2Receptors, Purinergic P2Y1Receptors, Purinergic P2Y2RNA, MessengerThionucleotidesUridine Triphosphateadenosine 5'-O-(2-thiotriphosphate)Adenosine TriphosphateChelating AgentsFluorescent DyesFura-2P2RY1 protein, humanP2RY2 protein, humanPurinergic P2 Receptor Agonistspurinoceptor P2Y4Receptors, Purinergic P2Receptors, Purinergic P2Y1Receptors, Purinergic P2Y2RNA, MessengerThionucleotidesUridine Triphosphate

Identifiers

PMID16025270
OpenAlexW1978714719

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.