Evidence map›Paper›PMID 19506088›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2009

Cell death-associated ADAMTS4 and versican degradation in vascular tissue.

Richard D Kenagy, Seung-Kee Min, Alexander W Clowes, John D Sandy

Open access · bronzeAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

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  8. Pathogenic mechanisms and the potential of drug therapies for aortic aneurysm.American journal of physiology. Heart and circulatory physiology · 2020
    Review
  9. A role for proteoglycans in vascular disease.Matrix biology : journal of the International Society for Matrix Biology · 2018
    Review
  10. Role of ADAMTS-5 in Aortic Dilatation and Extracellular Matrix Remodeling.Arteriosclerosis, thrombosis, and vascular biology · 2018
    Article
  11. Article
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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

4 authors at 2 institutions in 1 country.

Richard D KenagyCenter for Cardiovascular Biology, PO Box 358050, University of Washington School of Medicine, 815 Mercer St., Seattle, WA 98109. rkenagy@u.washington.edu.
Seung-Kee Min
Alexander W Clowes
John D Sandy
University of Washington · USRush University · US

Funding

YILMA SIV VACCINIA VACCINE TRIALP51RR000166 · NCRR · UNIVERSITY OF WASHINGTON · PI HU, SHIU-LOK · 1985 to 2011
$161.1M
CARDIOVASCULAR RESEARCH TRAINING PROGRAMT32HL007828 · NHLBI · UNIVERSITY OF WASHINGTON · PI Francis Kim, Farid Moussavi-Harami · 1997 to 2026
$10.2M
MECHANISMS OF ARTERIAL GRAFT HEALINGR01HL030946 · NHLBI · UNIVERSITY OF WASHINGTON · PI SOBEL, MICHAEL · 1985 to 2015
$7.3M
NCRR NIH HHS P51 RR000166NHLBI NIH HHS R01 HL030946NHLBI NIH HHS T32 HL007828
6 · The paper itself

Abstract

High blood flow through baboon polytetrafluorethylene aorto-iliac grafts increases neointimal vascular smooth muscle cell (SMC) death, neointimal atrophy, and cleavage of versican to generate the DPEAAE neoepitope, a marker of ADAMTS-mediated proteolysis. In this study, we have determined the effect of high blood flow on transcript abundance in the neointima for ADAMTS1, -4, -5, -8, -9, -15, and -20. We found that after 24 hr of flow, the mRNA for ADAMTS4 was significantly increased, whereas that for the other family members was unchanged. Because vascular SMC death is markedly increased in the graft after 24 hr of high flow, we next examined the possibility that the ADAMTS4 induction and the cell death are causally related. The addition of Fas ligand to SMC cultures increased both ADAMTS4 mRNA and cell death approximately 5-fold, consistent with the idea that ADAMTS4-dependent cleavage of versican may be partly responsible for cell death and tissue atrophy under these conditions.

Indexed as

ADAM ProteinsAnimalsAorta, AbdominalAorta, ThoracicAtrophyBlood Vessel ProsthesisCell DeathCells, CulturedDisease Models, AnimalFas Ligand ProteinHumansIliac ArteryMaleMuscle, Smooth, VascularMyocytes, Smooth MusclePapio cynocephalusADAM ProteinsFas Ligand ProteinPolytetrafluoroethyleneRNA, MessengerVersicans

Identifiers

PMID19506088
PMCPMC2728133
OpenAlexW1974344071

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.