Evidence map›Paper›PMID 20067788›Full record

ArticleExperimental cell research2010

Mesenchymal cells stimulate capillary morphogenesis via distinct proteolytic mechanisms.

Cyrus M Ghajar, Suraj Kachgal, Ekaterina Kniazeva, Hidetoshi Mori, Sylvain V Costes, Steven C George, Andrew J Putnam

Open access · greenAbstract read
In one paragraph

Article in Experimental cell research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

98 citing papers in PubMed, 156 citations in OpenAlex.

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38 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Cyrus M GhajarDepartment of Biomedical Engineering, University of California, Irvine, Irvine, CA 92697, USA.
Suraj Kachgal
Ekaterina Kniazeva
Hidetoshi Mori
Sylvain V Costes
Steven C George
Andrew J Putnam
University of California, Irvine · USLawrence Berkeley National Laboratory · US

Funding

Regulation and Enhancement of Angiogenesis in Dense Fibrin MatricesR01HL085339 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTNAM, ANDREW J · 2007 to 2024
$5.4M
Mechanisms of Subepithelial Fibrosis in AsthmaR01HL067954 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI GEORGE, STEVEN CARL · 2003 to 2012
$3.7M
NHLBI NIH HHS R01 HL067954NHLBI NIH HHS R01HL067954NHLBI NIH HHS R01 HL085339NHLBI NIH HHS R01HL085339
6 · The paper itself

Abstract

During angiogenesis, endothelial cells (ECs) degrade their surrounding extracellular matrix (ECM) to facilitate invasion. How interactions between ECs and other cells within their microenvironment facilitate this process is only partially understood. We have utilized a tractable 3D co-culture model to investigate the proteolytic mechanisms by which pre-committed or more highly committed mesenchymal cells stimulate capillary formation. On their own, ECs invade their surrounding matrix, but do not form capillaries. However, in the presence of either mesenchymal stem cells (MSCs) or fibroblasts, ECs form polarized, tubular structures that are intimately associated with mesenchymal cells. Further, ECs up-regulate gene expression of several extracellular proteases upon co-culture with either mesenchymal cell type. The administration of both broad spectrum and specific protease inhibitors demonstrated that MSC-stimulated capillary formation relied solely on membrane-type matrix metalloproteinases (MT-MMPs) while fibroblast-mediated sprouting proceeded independent of MMP inhibition unless the plasminogen activator/plasmin axis was inhibited in concert. While other studies have established a role for the ECM itself in dictating proteolysis and matrix degradation during capillary morphogenesis, the present study illustrates that heterotypic cellular interactions within the microenvironment can direct the proteolytic mechanisms required for capillary formation.

Indexed as

CapillariesCells, CulturedCoculture TechniquesEndothelial CellsExtracellular MatrixFibroblastsHumansHydrolysisMesodermMorphogenesisNeovascularization, PhysiologicProtease InhibitorsRNAProtease InhibitorsRNA

Identifiers

PMID20067788
PMCPMC2845480
OpenAlexW2115368694

What OpenQuestion holds

Textmetadata
LicenceTDM
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.