Evidence map›Paper›PMID 9410905›Full record

ArticleThe Journal of clinical investigation1997

Tissue factor expression in human arterial smooth muscle cells. TF is present in three cellular pools after growth factor stimulation.

A D Schecter, P L Giesen, O Taby, C L Rosenfield, M Rossikhina, B S Fyfe, D S Kohtz, J T Fallon, Y Nemerson, M B Taubman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 146 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Exosomes and Atherogenesis.Frontiers in cardiovascular medicine · 2021
    Review
  8. Review
  9. Article
  10. PDGF Restores the Defective Phenotype of Adipose-Derived Mesenchymal Stromal Cells from Diabetic Patients.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Host cell invasion by Staphylococcus aureus stimulates the shedding of microvesicles.Biochemical and biophysical research communications · 2013
    Article
  17. Article
  18. Review
  19. Tissue factor-bearing microparticles and thrombus formation.Arteriosclerosis, thrombosis, and vascular biology · 2011
    Review
  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

10 authors at 2 institutions in 1 country.

A D SchecterThe Cardiovascular Institute, Department of Medicine, The Mount Sinai School of Medicine, New York 10029, USA.
P L Giesen
O Taby
C L Rosenfield
M Rossikhina
B S Fyfe
D S Kohtz
J T Fallon
Y Nemerson
M B Taubman
Icahn School of Medicine at Mount Sinai · USMount Sinai Hospital · US

Funding

TISSUE FACTOR, THROMBOSIS AND THE ARTERIAL WALLP50HL054469 · NHLBI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BADIMON, JUAN JOSE · 1996 to 2005
$11.5M
TISSUE FACTOR IN BLOOD COAGULATIONP01HL029019 · NHLBI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GUHA, ARABINDA · 1985 to 2002
$5.8M
TISSUE FACTOR EXPRESSION &REGULATION IN ARTERIAL INJURYF32HL009402 · NHLBI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SCHECTER, ALISON D · 1995 to 1997
–
NHLBI NIH HHS HL09402NHLBI NIH HHS HL29019NHLBI NIH HHS HL54469
6 · The paper itself

Abstract

Tissue factor (TF) is a transmembrane glycoprotein that initiates the coagulation cascade. Because of the potential role of TF in mediating arterial thrombosis, we have examined its expression in human aortic and coronary artery smooth muscle cells (SMC). TF mRNA and protein were induced in SMC by a variety of growth agonists. Exposure to PDGF AA or BB for 30 min provided all of the necessary signals for induction of TF mRNA and protein. This result was consistent with nuclear runoff analyses, demonstrating that PDGF-induced TF transcription occurred within 30 min. A newly developed assay involving binding of digoxigenin-labeled FVIIa (DigVIIa) and digoxigenin-labeled Factor X (DigX) was used to localize cellular TF. By light and confocal microscopy, prominent TF staining was seen in the perinuclear cytoplasm beginning 2 h after agonist treatment and persisting for 10-12 h. Surface TF activity, measured on SMC monolayers under flow conditions, increased transiently, peaking 4-6 h after agonist stimulation and returning to baseline within 16 h. Peak surface TF activity was only approximately 20% of total TF activity measured in cell lysates. Surface TF-blocking experiments demonstrated that the remaining TF was found as encrypted surface TF, and also in an intracellular pool. The relatively short-lived surface expression of TF may be critical for limiting the thrombotic potential of intact SMC exposed to growth factor stimulation. In contrast, the encrypted surface and intracellular pools may provide a rich source of TF under conditions associated with SMC damage, such as during atherosclerotic plaque rupture or balloon arterial injury.

Indexed as

AortaCell CompartmentationCells, CulturedFactor VIIaFactor XGene ExpressionHumansMuscle, Smooth, VascularPlatelet-Derived Growth FactorRheologyRNA, MessengerThromboplastinTranscription, GeneticFactor VIIaFactor XPlatelet-Derived Growth FactorRNA, MessengerThromboplastin

Identifiers

PMID9410905
PMCPMC508423
OpenAlexW2078372594

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.