Evidence map›Paper›PMID 34360685›Full record

ArticleInternational journal of molecular sciences2021

Long-Term Severe In Vitro Hypoxia Exposure Enhances the Vascularization Potential of Human Adipose Tissue-Derived Stromal Vascular Fraction Cell Engineered Tissues.

Myroslava Mytsyk, Giulia Cerino, Gregory Reid, Laia Gili Sole, Friedrich S Eckstein, David Santer, Anna Marsano

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Myroslava MytsykDepartment of Cardiac Surgery, University Hospital Basel, 4031 Basel, Switzerland.
Giulia CerinoDepartment of Cardiac Surgery, University Hospital Basel, 4031 Basel, Switzerland.
Gregory ReidDepartment of Cardiac Surgery, University Hospital Basel, 4031 Basel, Switzerland.ORCID 0000-0003-2089-3830
Laia Gili SoleDepartment of Cardiac Surgery, University Hospital Basel, 4031 Basel, Switzerland.ORCID 0000-0003-2601-2061
Friedrich S EcksteinDepartment of Cardiac Surgery, University Hospital Basel, 4031 Basel, Switzerland.
David SanterDepartment of Cardiac Surgery, University Hospital Basel, 4031 Basel, Switzerland.ORCID 0000-0003-4493-4326
Anna MarsanoDepartment of Cardiac Surgery, University Hospital Basel, 4031 Basel, Switzerland.
University Hospital of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The therapeutic potential of mesenchymal stromal/stem cells (MSC) for treating cardiac ischemia strongly depends on their paracrine-mediated effects and their engraftment capacity in a hostile environment such as the infarcted myocardium. Adipose tissue-derived stromal vascular fraction (SVF) cells are a mixed population composed mainly of MSC and vascular cells, well known for their high angiogenic potential. A previous study showed that the angiogenic potential of SVF cells was further increased following their in vitro organization in an engineered tissue (patch) after perfusion-based bioreactor culture. This study aimed to investigate the possible changes in the cellular SVF composition, in vivo angiogenic potential, as well as engraftment capability upon in vitro culture in harsh hypoxia conditions. This mimics the possible delayed vascularization of the patch upon implantation in a low perfused myocardium. To this purpose, human SVF cells were seeded on a collagen sponge, cultured for 5 days in a perfusion-based bioreactor under normoxia or hypoxia (21% and <1% of oxygen tension, respectively) and subcutaneously implanted in nude rats for 3 and 28 days. Compared to ambient condition culture, hypoxic tension did not alter the SVF composition in vitro, showing similar numbers of MSC as well as endothelial and mural cells. Nevertheless, in vitro hypoxic culture significantly increased the release of vascular endothelial growth factor (

Indexed as

Cell DifferentiationHypoxiaNeovascularization, PhysiologicAdipose TissueCells, CulturedHumansMesenchymal Stem CellsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Aengineered tissueshypoxic culturein vivo angiogenesisstromal vascular fraction cells

Identifiers

PMID34360685
PMCPMC8348696
OpenAlexW3185827090

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.