Evidence map›Paper›PMID 25800869›Full record

ArticleBiochemical and biophysical research communications2015

Fluid shear stress promotes proprotein convertase-dependent activation of MT1-MMP.

Hojin Kang, Camille L Duran, Colette A Abbey, Roland R Kaunas, Kayla J Bayless

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
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  9. Article
  10. Piezo1 mediates angiogenesis through activation of MT1-MMP signaling.American journal of physiology. Cell physiology · 2019
    Article
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  13. Review
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

5 authors at 2 institutions in 1 country.

Hojin KangMolecular & Cellular Medicine, Texas A&M Health Science Center, College Station, TX, USA.
Camille L DuranMolecular & Cellular Medicine, Texas A&M Health Science Center, College Station, TX, USA.
Colette A AbbeyMolecular & Cellular Medicine, Texas A&M Health Science Center, College Station, TX, USA.
Roland R KaunasDepartment of Biomedical Engineering, Texas A&M University, College Station, TX, USA.
Kayla J BaylessMolecular & Cellular Medicine, Texas A&M Health Science Center, College Station, TX, USA. Electronic address: kbayless@medicine.tamhsc.edu.
Texas A&M Health Science Center · USTexas A&M University · US

Funding

Mechanisms of Angiogenic Switch Activation During Wound RepairR01HL095786 · NHLBI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI BAYLESS, KAYLA J · 2010 to 2014
$1.8M
NHLBI NIH HHS HL095786NHLBI NIH HHS R01 HL095786
6 · The paper itself

Abstract

During angiogenesis, endothelial cells (ECs(1)) initiate new blood vessel growth and invade into the extracellular matrix (ECM). Membrane type-1 matrix metalloproteinase (MT1-MMP) facilitates this process and translocates to the plasma membrane following activation to promote ECM cleavage. The N-terminal pro-domain within MT1-MMP must be processed for complete activity of the proteinase. This study investigated whether MT1-MMP activation was altered by sphingosine 1-phosphate (S1P) and wall shear stress (WSS), which combine to stimulate EC invasion in three dimensional (3D) collagen matrices. MT1-MMP was activated rapidly and completely by WSS but not S1P. Proprotein convertases (PCs) promoted MT1-MMP processing, prompting us to test whether WSS or S1P treatments increased PC activity. Like MT1-MMP, PC activity increased with WSS, while S1P had no effect. A pharmacological PC inhibitor completely blocked S1P- and WSS-induced EC invasion and MT1-MMP translocation to the plasma membrane. Further, a recombinant PC inhibitor reduced MT1-MMP activation and decreased lumen formation in invading ECs, a process known to be controlled by MT1-MMP. Thus, we conclude that PC and MT1-MMP activation are mechanosensitive events that are required for EC invasion into 3D collagen matrices.

Indexed as

Stress, MechanicalEnzyme ActivationHumansHuman Umbilical Vein Endothelial CellsMatrix Metalloproteinase 14Proprotein ConvertasesMatrix Metalloproteinase 14MMP14 protein, humanProprotein ConvertasesAngiogenesisFurinMechanotransductionSprouting

Identifiers

PMID25800869
PMCPMC4428763
OpenAlexW1996516927

What OpenQuestion holds

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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.