Evidence map›Paper›PMID 10049948›Full record

ArticleThe Journal of experimental medicine1999

Expression of stromelysin-3 in atherosclerotic lesions: regulation via CD40-CD40 ligand signaling in vitro and in vivo.

U Schönbeck, F Mach, G K Sukhova, E Atkinson, E Levesque, M Herman, P Graber, P Basset, P Libby

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 153 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. CD40L and Its Receptors in Atherothrombosis-An Update.Frontiers in cardiovascular medicine · 2017
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Clinical study of the hypothesis of endogenous collateral wind on acute coronary syndrome: a review.African journal of traditional, complementary, and alternative medicines : AJTCAM · 2014
    Review
  12. Review
  13. The role of matrix metalloproteinases in atherothrombosis.Current atherosclerosis reports · 2011
    Review
  14. Review
  15. Macrophage heterogeneity in atherosclerotic plaques.Current opinion in lipidology · 2009
    Review
  16. Article
  17. Article
  18. Review
  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

9 authors at 2 institutions in 1 country.

U SchönbeckVascular Medicine and Atherosclerosis Unit, Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
F Mach
G K Sukhova
E Atkinson
E Levesque
M Herman
P Graber
P Basset
P Libby
Brigham and Women's Hospital · USHarvard University · US

Funding

PATHOGENESIS OF TRANSPLANT-ASSOCIATED ARTERIOSCLEROSISR01HL043364 · NHLBI · TUFTS MEDICAL CENTER · PI MITCHELL, RICHARD N · 1990 to 2003
$1.2M
NHLBI NIH HHS HL-43364
6 · The paper itself

Abstract

Stromelysin-3 is an unusual matrix metalloproteinase, being released in the active rather than zymogen form and having a distinct substrate specificity, targeting serine proteinase inhibitors (serpins), which regulate cellular functions involved in atherosclerosis. We report here that human atherosclerotic plaques (n = 7) express stromelysin-3 in situ, whereas fatty streaks (n = 5) and normal arterial specimens (n = 5) contain little or no stromelysin-3. Stromelysin-3 mRNA and protein colocalized with endothelial cells, smooth muscle cells, and macrophages within the lesion. In vitro, usual inducers of matrix metalloproteinases such as interleukin-1, interferon-gamma, or tumor necrosis factor alpha did not augment stromelysin-3 in vascular wall cells. However, T cell-derived as well as recombinant CD40 ligand (CD40L, CD154), an inflammatory mediator recently localized in atheroma, induced de novo synthesis of stromelysin-3. In addition, stromelysin-3 mRNA and protein colocalized with CD40L and CD40 within atheroma. In accordance with the in situ and in vitro data obtained with human material, interruption of the CD40-CD40L signaling pathway in low density lipoprotein receptor-deficient hyperlipidemic mice substantially decreased expression of the enzyme within atherosclerotic plaques. These observations establish the expression of the unusual matrix metalloproteinase stromelysin-3 in human atherosclerotic lesions and implicate CD40-CD40L signaling in its regulation, thus providing a possible new pathway that triggers complications within atherosclerotic lesions.

Indexed as

AnimalsAortaArteriosclerosisCarotid ArteriesCD40 AntigensCD40 LigandEndothelium, VascularHumansHyperlipidemiasMacrophagesMatrix Metalloproteinase 11Membrane GlycoproteinsMetalloendopeptidasesMiceMice, Mutant StrainsMuscle, Smooth, VascularCD40 AntigensCD40 LigandMatrix Metalloproteinase 11Membrane GlycoproteinsMetalloendopeptidasesReceptors, LDL

Identifiers

PMID10049948
PMCPMC2192948
OpenAlexW2162474560

What OpenQuestion holds

Texttitle and abstract
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.