Evidence map›Paper›PMID 19465549›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2009

Interstitial flow promotes vascular fibroblast, myofibroblast, and smooth muscle cell motility in 3-D collagen I via upregulation of MMP-1.

Zhong-Dong Shi, Xin-Ying Ji, Henry Qazi, John M Tarbell

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2009. 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 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

57 citing papers in PubMed, 96 citations in OpenAlex.

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  13. Mechanical regulation of the early stages of angiogenesis.Journal of the Royal Society, Interface · 2022
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Zhong-Dong ShiDepartment of Biomedical Engineering, City College of New York, City University of New York, New York 10031, USA.
Xin-Ying Ji
Henry Qazi
John M Tarbell
City College of New York · US

Funding

WALL SHEAR STRESS IN THE CARDIOVASCULAR SYSTEMR01HL035549 · NHLBI · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI TARBELL, JOHN M · 1986 to 2003
$1.1M
NHLBI NIH HHS HL-35549NHLBI NIH HHS HL-57093
6 · The paper itself

Abstract

Neointima formation often occurs in regions where the endothelium has been damaged and the transmural interstitial flow is elevated. Vascular smooth muscle cells (SMCs) and fibroblasts/myofibroblasts (FBs/MFBs) contribute to intimal thickening by migrating from the media and adventitia into the site of injury. In this study, for the first time, the direct effects of interstitial flow on SMC and FB/MFB migration were investigated in an in vitro three-dimensional system. Collagen I gels were used to mimic three-dimensional extracellular matrix (ECM) for rat aortic SMCs and FBs/MFBs. Exposure to interstitial flow induced by 1 cmH(2)O pressure differential (shear stress, approximately 0.05 dyn/cm(2); flow velocity, approximately 0.5 microm/s; and Darcy permeability, approximately 10(-11) cm(2)) substantially enhanced cell motility. Matrix metalloproteinase (MMP) inhibitor (GM-6001) abolished flow-induced migration augmentation, which suggested that the enhanced motility was MMP dependent. The upregulation of MMP-1 played a critical role for the flow-enhanced motility, which was further confirmed by silencing MMP-1 gene expression. Longer exposures to higher flows suppressed the number of migrated cells, although MMP-1 gene expression remained high. This suppression was a result of both flow-induced tissue inhibitor of metalloproteinase-1 upregulation and increased apoptotic and necrotic cell death. Interstitial flow did not affect MMP-2 gene expression or activity in the collagen I gel for any cell type. Our findings shed light on the mechanism by which vascular SMCs and FBs/MFBs contribute to intimal thickening in regions of vascular injury where interstitial flow is elevated.

Indexed as

Cell MovementMechanotransduction, CellularPulsatile FlowAnimalsApoptosisBlood PressureCells, CulturedCollagen Type IDipeptidesFibroblastsGelsMatrix Metalloproteinase 1Matrix Metalloproteinase 2Matrix Metalloproteinase InhibitorsModels, BiologicalMuscle, Smooth, VascularCollagen Type IDipeptidesGelsMatrix Metalloproteinase 1Matrix Metalloproteinase 2Matrix Metalloproteinase InhibitorsMmp2 protein, ratN-(2(R)-2-(hydroxamidocarbonylmethyl)-4-methylpentanoyl)-L-tryptophan methylamideProtease InhibitorsTissue Inhibitor of Metalloproteinase-1

Identifiers

PMID19465549
PMCPMC2770759
OpenAlexW2130214432

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.