Evidence map›Paper›PMID 21071745›Full record

ArticleInvestigative ophthalmology & visual science2011

Activation of P2X receptors induces apoptosis in human retinal pigment epithelium.

Dongli Yang, Susan G Elner, Andrea J Clark, Bret A Hughes, Howard R Petty, Victor M Elner

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-weighted citation impact, top 11% 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

31 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Role of P2X7R in Retinal Diseases: A Review.Immunity, inflammation and disease · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. Osmotic regulation ofMolecular vision · 2017
    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 3 institutions in 2 countries.

Dongli YangDepartment of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, Michigan 48105-0714, USA.
Susan G Elner
Andrea J Clark
Bret A Hughes
Howard R Petty
Victor M Elner
Bipar · FRLaboratoire d’immunologie intégrative du cancer · FRUniversity of Michigan–Ann Arbor · US

Funding

VIVARIUM MODULEP30EY007003 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI David Antonetti · 1987 to 2026
$17.6M
ION CONDUCTANCES IN THE RETINAL PIGMENT EPITHELIUMR01EY008850 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HUGHES, BRET A · 1991 to 2017
$6.8M
RPE-Mphi Binding: Ca++_&O2-_Dependent AMD ResponsesR01EY009441 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELNER, VICTOR M · 1992 to 2008
$3.2M
Signaling Dynamics of Leukocyte-Tumor Cell InteractionsR01CA074120 · NCI · WAYNE STATE UNIVERSITY · PI PETTY, HOWARD R · 1998 to 2008
$2.1M
NCI NIH HHS CA74120NCI NIH HHS R01 CA074120NEI NIH HHS EY08850NEI NIH HHS EY09441NEI NIH HHS P30 EY007003NEI NIH HHS P30EY07003NEI NIH HHS R01 EY008850NEI NIH HHS R01 EY009441
6 · The paper itself

Abstract

purposeThe retinal pigment epithelium (RPE) is considered a primary site of pathology in age-related macular degeneration (AMD), which is the most prevalent form of irreversible blindness worldwide in the elderly population. Extracellular adenosine triphosphate (ATP) acts as a key signaling molecule in numerous cellular processes, including cell death. The purpose of this study was to determine whether extracellular ATP induces apoptosis in cultured human RPE.

methodsRPE apoptosis was evaluated by caspase-3 activation, Hoechst staining, and DNA fragmentation. Intracellular Ca(2+) levels were determined by both a cell-based fluorometric Ca(2+) assay and a ratiometric Ca(2+) imaging technique. P2X(7) mRNA and protein expression were detected by reverse transcription-polymerase chain reaction (RT-PCR) and confocal microscopy, respectively.

resultsThe authors found that both the endogenous P2X(7) agonist ATP and the synthetic, selective P2X(7) agonist 2',3'-O-(4-benzoylbenzoyl)-ATP (BzATP) induced RPE apoptosis, which was significantly inhibited by P2X(7) antagonist oxidized ATP (oATP) but not by the P2 receptor antagonist suramin; both ATP and BzATP increase intracellular Ca(2+) via extracellular Ca(2+) influx; both ATP- and BzATP-induced Ca(2+) responses were significantly inhibited by oATP but not by suramin; ATP-induced apoptosis was significantly inhibited or blocked by BAPTA-AM or by low or no extracellular Ca(2+); and P2X(7) receptor mRNA and protein were expressed in RPE cells.

conclusionsThese findings suggest that P2X receptors, especially P2X(7) receptors, contribute to ATP- and BzATP-induced Ca(2+) signaling and apoptosis in the RPE. Abnormal Ca(2+) homeostasis through the activation of P2X receptors could cause the dysfunction and apoptosis of RPE that underlie AMD.

Indexed as

Adenosine TriphosphateApoptosisCalciumCalcium SignalingCaspase 3Cells, CulturedDNA FragmentationEnzyme ActivationEnzyme-Linked Immunosorbent AssayFluorometryHumansMicroscopy, ConfocalReceptors, Purinergic P2XRetinal Pigment EpitheliumReverse Transcriptase Polymerase Chain ReactionRNA, Messenger3'-O-(4-benzoyl)benzoyladenosine 5'-triphosphateAdenosine TriphosphateCalciumCaspase 3Receptors, Purinergic P2XRNA, Messenger

Identifiers

PMID21071745
PMCPMC3101688
OpenAlexW2004380591

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.