Evidence map›Paper›PMID 29079730›Full record

ArticleScientific reports2017

Engineering of an angiogenic niche by perfusion culture of adipose-derived stromal vascular fraction cells.

Giulia Cerino, Emanuele Gaudiello, Manuele Giuseppe Muraro, Friedrich Eckstein, Ivan Martin, Arnaud Scherberich, Anna Marsano

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

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  9. Culturing patient-derived malignant hematopoietic stem cells in engineered and fully humanized 3D niches.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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.

Giulia CerinoDepartments of Biomedicine and Surgery, University of Basel and University Hospital of Basel, 4031, Basel, Switzerland.
Emanuele GaudielloDepartments of Biomedicine and Surgery, University of Basel and University Hospital of Basel, 4031, Basel, Switzerland.
Manuele Giuseppe MuraroDepartments of Biomedicine and Surgery, University of Basel and University Hospital of Basel, 4031, Basel, Switzerland.
Friedrich EcksteinDepartments of Biomedicine and Surgery, University of Basel and University Hospital of Basel, 4031, Basel, Switzerland.
Ivan MartinDepartments of Biomedicine and Surgery, University of Basel and University Hospital of Basel, 4031, Basel, Switzerland.
Arnaud ScherberichDepartments of Biomedicine and Surgery, University of Basel and University Hospital of Basel, 4031, Basel, Switzerland.ORCID 0000-0003-3468-6955
Anna MarsanoDepartments of Biomedicine and Surgery, University of Basel and University Hospital of Basel, 4031, Basel, Switzerland. anna.marsano@usb.ch.
University of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In vitro recapitulation of an organotypic stromal environment, enabling efficient angiogenesis, is crucial to investigate and possibly improve vascularization in regenerative medicine. Our study aims at engineering the complexity of a vascular milieu including multiple cell-types, a stromal extracellular matrix (ECM), and molecular signals. For this purpose, the human adipose stromal vascular fraction (SVF), composed of a heterogeneous mix of pericytes, endothelial/stromal progenitor cells, was cultured under direct perfusion flow on three-dimensional (3D) collagen scaffolds. Perfusion culture of SVF-cells reproducibly promoted in vitro the early formation of a capillary-like network, embedded within an ECM backbone, and the release of numerous pro-angiogenic factors. Compared to static cultures, perfusion-based engineered constructs were more rapidly vascularized and supported a superior survival of delivered cells upon in vivo ectopic implantation. This was likely mediated by pericytes, whose number was significantly higher (4.5-fold) under perfusion and whose targeted depletion resulted in lower efficiency of vascularization, with an increased host foreign body reaction. 3D-perfusion culture of SVF-cells leads to the engineering of a specialized milieu, here defined as an angiogenic niche. This system could serve as a model to investigate multi-cellular interactions in angiogenesis, and as a module supporting increased grafted cell survival in regenerative medicine.

Indexed as

Neovascularization, PhysiologicAdipose TissueAnimalsCell Culture TechniquesCell EngineeringCell ProliferationExtracellular SpaceHumansMalePerfusionRatsStromal Cells

Identifiers

PMID29079730
PMCPMC5660248
OpenAlexW2766469206

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.