Evidence map›Paper›PMID 35163683›Full record

ArticleInternational journal of molecular sciences2022

Extracellular Matrix Synthesis and Remodeling by Mesenchymal Stromal Cells Is Context-Sensitive.

Janina Burk, Anna Sassmann, Cornelia Kasper, Ariane Nimptsch, Susanna Schubert

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
3.8field-weighted citation impact, top 6% 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, 28 citations in OpenAlex.

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  17. Perspectives of Proteomics in Respiratory Allergic Diseases.International journal of molecular sciences · 2023
    Review
  18. Mesodermal Derivatives of Pluripotent Stem Cells Route to Scarless Healing.International journal of molecular sciences · 2023
    Review
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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

5 authors at 3 institutions in 2 countries.

Janina BurkEquine Clinic (Surgery, Orthopedics), Justus-Liebig-University Giessen, 35392 Giessen, Germany.ORCID 0000-0002-7868-0355
Anna SassmannInstitute for Cell and Tissue Culture Technologies, Department of Biotechnology, University of Natural Resources and Life Sciences (BOKU), 1190 Vienna, Austria.
Cornelia KasperInstitute for Cell and Tissue Culture Technologies, Department of Biotechnology, University of Natural Resources and Life Sciences (BOKU), 1190 Vienna, Austria.ORCID 0000-0003-2607-4326
Ariane NimptschInstitute for Medical Physics and Biophysics, University of Leipzig, 04107 Leipzig, Germany.
Susanna SchubertInstitute of Human Genetics, University of Leipzig, 04103 Leipzig, Germany.ORCID 0000-0003-2299-1311
BOKU University · ATLeipzig University · DEJustus-Liebig-Universität Gießen · DE

Funding

Deutsche Forschungsgemeinschaft NI 1396/3-2
6 · The paper itself

Abstract

Matrix remodeling could be an important mode of action of multipotent mesenchymal stromal cells (MSC) in extracellular matrix (ECM) disease, but knowledge is limited in this respect. As MSC are well-known to adapt their behavior to their environment, we aimed to investigate if their mode of action would change in response to healthy versus pathologically altered ECM. Human MSC-derived ECM was produced under different culture conditions, including standard culture, culture on Matrigel-coated dishes, and stimulation with the pro-fibrotic transforming growth factor-β1 (TGFβ1). The MSC-ECM was decellularized, characterized by histochemistry, and used as MSC culture substrate reflecting different ECM conditions. MSC were cultured on the different ECM substrates or in control conditions for 2 days. Culture on ECM increased the presence of surface molecules with ECM receptor function in the MSC, demonstrating an interaction between MSC and ECM. In MSC cultured on Matrigel-ECM and TGFβ1-ECM, which displayed a fibrosis-like morphology, gene expression of collagens and decorin, as well as total matrix metalloproteinase (MMP) activity in the supernatant were decreased as compared with control conditions. These results demonstrated that MSC adapt to their ECM environment, which may include pathological adaptations that could compromise therapeutic efficacy.

Indexed as

Cells, CulturedCell SurvivalCytoskeletonExtracellular MatrixGene Expression RegulationHumansMatrix MetalloproteinasesMesenchymal Stem CellsReceptors, Cell SurfaceSubstrate SpecificityTissue Inhibitor of MetalloproteinasesMatrix MetalloproteinasesReceptors, Cell SurfaceTissue Inhibitor of Metalloproteinasescollagenextracellular matrix (ECM)matrisomematrix metalloproteinases (MMP)matrix remodelingmesenchymal stromal cells (MSC)mode of actionMSC-derived ECMtissue-inhibitors-of-matrix-metalloproteinases (TIMP)

Identifiers

PMID35163683
PMCPMC8836208
OpenAlexW4210521906

What OpenQuestion holds

Textmetadata
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.