Evidence map›Paper›PMID 23236386›Full record

ArticlePloS one2012

Effect of lumican on the migration of human mesenchymal stem cells and endothelial progenitor cells: involvement of matrix metalloproteinase-14.

Mariusz Malinowski, Katarzyna Pietraszek, Corinne Perreau, Mateusz Boguslawski, Véronique Decot, Jean-François Stoltz, Laurent Vallar, Jolanta Niewiarowska, Czeslaw Cierniewski, François-Xavier Maquart and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.0field-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

26 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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  9. Communications via the Small Leucine-rich Proteoglycans: Molecular Specificity in Inflammation and Autoimmune Diseases.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2020
    Review
  10. In vitro and bioinformatics mechanistic-based approach for cadmium carcinogenicity understanding.Toxicology in vitro : an international journal published in association with BIBRA · 2020
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

12 authors at 8 institutions in 3 countries.

Mariusz MalinowskiLaboratoire de Biochimie Médicale et de Biologie Moléculaire, CNRS FRE 3481, Université de Reims Champagne-Ardenne, Reims, France.
Katarzyna Pietraszek
Corinne Perreau
Mateusz Boguslawski
Véronique Decot
Jean-François Stoltz
Laurent Vallar
Jolanta Niewiarowska
Czeslaw Cierniewski
François-Xavier Maquart
Yanusz Wegrowski
Stéphane Brézillon
Centre National de la Recherche Scientifique · FRUniversité de Reims Champagne-Ardenne · FRCentre de Médecine Préventive · FRCentre Hospitalier Universitaire de Reims · FRInstitute for Medical Biology · PLLaboratoire National de Santé · LUMedical University of Lodz · PLUniversité de Lorraine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIncreasing number of evidence shows that soluble factors and extracellular matrix (ECM) components provide an optimal microenvironment controlling human bone marrow mesenchymal stem cell (MSC) functions. Successful in vivo administration of stem cells lies in their ability to migrate through ECM barriers and to differentiate along tissue-specific lineages, including endothelium. Lumican, a protein of the small leucine-rich proteoglycan (SLRP) family, was shown to impede cell migration and angiogenesis. The aim of the present study was to analyze the role of lumican in the control of MSC migration and transition to functional endothelial progenitor cell (EPC). METHODOLOGY/PRINCIPAL

findingsLumican inhibited tube-like structures formation on Matrigel® by MSC, but not EPC. Since matrix metalloproteinases (MMPs), in particular MMP-14, play an important role in remodelling of ECM and enhancing cell migration, their expression and activity were investigated in the cells grown on different ECM substrata. Lumican down-regulated the MMP-14 expression and activity in MSC, but not in EPC. Lumican inhibited MSC, but not EPC migration and invasion. The inhibition of MSC migration and invasion by lumican was reversed by MMP-14 overexpression. CONCLUSION/SIGNIFICANCE: Altogether, our results suggest that lumican inhibits MSC tube-like structure formation and migration via mechanisms that involve a decrease of MMP-14 expression and activity.

Indexed as

ApoptosisCell DifferentiationCell MovementCell ProliferationCells, CulturedChondroitin Sulfate ProteoglycansDown-RegulationEndothelial CellsHumansKeratan SulfateLumicanMatrix Metalloproteinase 14Mesenchymal Stem CellsTissue Inhibitor of Metalloproteinase-1Tissue Inhibitor of Metalloproteinase-3Chondroitin Sulfate ProteoglycansKeratan SulfateLumicanLUM protein, humanMatrix Metalloproteinase 14Tissue Inhibitor of Metalloproteinase-1Tissue Inhibitor of Metalloproteinase-3

Identifiers

PMID23236386
PMCPMC3517548
OpenAlexW2050088905

What OpenQuestion holds

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LicenceCC BY
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.