Evidence map›Paper›PMID 24040204›Full record

ArticlePloS one2013

TRAIL-deficiency accelerates vascular calcification in atherosclerosis via modulation of RANKL.

Belinda A Di Bartolo, Siân P Cartland, Hanis H Harith, Yuri V Bobryshev, Michael Schoppet, Mary M Kavurma

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Article
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  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. [miRNA-26a reduces vascular smooth muscle cell calcification by regulating connective tissue growth factor].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  11. Review
  12. Pro-Calcific Environment Impairs Ischaemia-Driven Angiogenesis.International journal of molecular sciences · 2022
    Article
  13. Review
  14. Article
  15. Article
  16. C/EBPβ is a key transcription factor of ox-LDL inducing THP-1 cells to release multiple pro-inflammatory cytokines.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    Article
  17. Review
  18. TRAIL signals, extracellular matrix and vessel remodelling.Vascular biology (Bristol, England) · 2020
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

6 authors at 2 institutions in 3 countries.

Belinda A Di BartoloCentre for Vascular Research, University of New South Wales, Sydney, NSW, Australia.
Siân P Cartland
Hanis H Harith
Yuri V Bobryshev
Michael Schoppet
Mary M Kavurma
UNSW Sydney · AUPhilips (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The osteoprotegerin (OPG) and receptor activator of nuclear factor-κB ligand (RANKL) cytokine system, not only controls bone homeostasis, but has been implicated in regulating vascular calcification. TNF-related apoptosis-inducing ligand (TRAIL) is a second ligand for OPG, and although its effect in vascular calcification in vitro is controversial, its role in vivo is not yet established. This study aimed to investigate the role of TRAIL in vascular calcification in vitro using vascular smooth muscle cells (VSMCs) isolated from TRAIL(-/-) and wild-type mice, as well as in vivo, in advanced atherosclerotic lesions of TRAIL(-/-)ApoE(-/-) mice. The involvement of OPG and RANKL in this process was also examined. TRAIL dose-dependently inhibited calcium-induced calcification of human VSMCs, while TRAIL(-/-) VSMCs demonstrated accelerated calcification induced by multiple concentrations of calcium compared to wild-type cells. Consistent with this, RANKL mRNA was significantly elevated with 24 h calcium treatment, while OPG and TRAIL expression in human VSMCs was inhibited. Brachiocephalic arteries from TRAIL(-/-)ApoE(-/-) and ApoE(-/-) mice fed a high fat diet for 12 w demonstrated increased chondrocyte-like cells in atherosclerotic plaque, as well as increased aortic collagen II mRNA expression in TRAIL(-/-)ApoE(-/-) mice, with significant increases in calcification observed at 20 w. TRAIL(-/-)ApoE(-/-) aortas also had significantly elevated RANKL, BMP-2, IL-1β, and PPAR-γ expression at 12 w. Our data provides the first evidence that TRAIL deficiency results in accelerated cartilaginous metaplasia and calcification in atherosclerosis, and that TRAIL plays an important role in the regulation of RANKL and inflammatory markers mediating bone turn over in the vasculature.

Indexed as

AnimalsAortaApolipoproteins EAtherosclerosisBrachiocephalic TrunkCalciumCells, CulturedChondrocytesCollagen Type IIDiet, High-FatGene Expression RegulationHumansMiceMice, KnockoutMuscle, Smooth, VascularMyocytes, Smooth MuscleApolipoproteins ECalciumCollagen Type IIOsteoprotegerinRANK LigandRNA, MessengerTNF-Related Apoptosis-Inducing LigandTNFRSF11B protein, human

Identifiers

PMID24040204
PMCPMC3764101
OpenAlexW1977668440

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.