Evidence map›Paper›PMID 3584243›Full record

ArticleThe Journal of cell biology1987

The platelet fibrinogen receptor: an immunogold-surface replica study of agonist-induced ligand binding and receptor clustering.

W M Isenberg, R P McEver, D R Phillips, M A Shuman, D F Bainton

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1987. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 184 citations in OpenAlex.

  1. Article
  2. Article
  3. The anticoagulant properties of cadmium telluride quantum dots.Journal of interdisciplinary nanomedicine · 2018
    Article
  4. RGDfK-functionalized gold nanorods bind only to activated platelets.Journal of biomedical materials research. Part A · 2017
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Disrupting integrin transmembrane domain heterodimerization increases ligand binding affinity, not valency or clustering.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  10. Article
  11. Article
  12. Article
  13. Expression of alpha v and beta 3 integrin chains on murine lymphocytes.Proceedings of the National Academy of Sciences of the United States of America · 1996
    Article
  14. Article
  15. Article
  16. Article
  17. Glycoprotein IIb-IIIa and the translocation of Rap2B to the platelet cytoskeleton.Proceedings of the National Academy of Sciences of the United States of America · 1994
    Article
  18. Article
  19. Article
  20. 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

5 authors.

W M Isenberg
R P McEver
D R Phillips
M A Shuman
D F Bainton

Funding

MATURATION AND FUNCTION OF BONE MARROW CELLSR01AM010486 · AM · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI BAINTON, DOROTHY F · 1985 to 1985
–
IMMUNOCHEMICAL LOCALIZATION OF MEGAKARYOCYTE PROTEINSR01HL031610 · NHLBI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI BAINTON, DOROTHY F · 1985 to 1985
–
IMMUNOCYTOCHEMISTRY OF MEGAKARYOCYTES AND PLATELETSR37HL031610 · NHLBI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI BAINTON, DOROTHY F · 1986 to 1995
–
NHLBI NIH HHS HL-31610NIADDK NIH HHS AM-10486
6 · The paper itself

Abstract

Platelet aggregation requires the binding of fibrinogen to its receptor, a heterodimer consisting of the plasma-membrane glycoproteins (GP) IIb and IIIa. Although the GPIIb-IIIa complex is present on the surface of unstimulated platelets, it binds fibrinogen only after platelet activation. We have used an immunogold-surface replica technique to study the distribution of GPIIb-IIIa and bound fibrinogen over broad areas of surface membranes in unstimulated, as well as thrombin-activated and ADP-activated human platelets. We found that the immunogold-labeled GPIIb-IIIa was monodispersed over the surface of unstimulated platelets, although the cell surface lacked immunoreactive fibrinogen. On thrombin-stimulated platelets, approximately 65% of the GPIIb-IIIa molecules were in clusters within the plane of the membrane. Fibrinogen, which had been released from the alpha-granules of these cells, bound to GPIIb-IIIa on the cell surface and was similarly clustered. To determine whether the receptors clustered before ligand binding, or as a consequence thereof, we studied the surface distribution of GPIIb-IIIa after stimulation with ADP, which causes activation of the fibrinogen receptor function of GPIIb-IIIa without inducing the release of fibrinogen. In the absence of added fibrinogen, the unoccupied, yet binding-competent receptors on ADP-stimulated platelets were monodispersed. The addition of fibrinogen caused the GPIIb-IIIa molecules to cluster on the cell surface. Clustering was also induced by the addition of the GPIIb-IIIa-binding domains of fibrinogen, namely the tetrapeptide Arg-Gly-Asp-Ser on the alpha-chain or the gamma-chain decapeptide gamma 402-411. These results show that receptor occupancy causes clustering of GPIIb-IIIa in activated platelets.

Indexed as

Adenosine DiphosphateBlood PlateletsCell MembraneFibrinogenHumansMicroscopy, ElectronPlatelet AggregationPlatelet Membrane GlycoproteinsReceptor AggregationThrombinAdenosine DiphosphateFibrinogenPlatelet Membrane GlycoproteinsThrombin

Identifiers

PMID3584243
PMCPMC2114491
OpenAlexW2010711286

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.