Evidence map›Paper›PMID 39796147›Full record

ArticleInternational journal of molecular sciences2024

Standardization to Characterize the Complexity of Vessel Network Using the Aortic Ring Model.

Petra Wolint, Silvan Hofmann, Julia von Atzigen, Roland Böni, Iris Miescher, Pietro Giovanoli, Maurizio Calcagni, Maximilian Y Emmert, Johanna Buschmann

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

9 authors.

Petra WolintDivision of Surgical Research, University Hospital of Zurich, 8091 Zurich, Switzerland.ORCID 0000-0002-9978-1438
Silvan HofmannDepartment of Plastic Surgery and Hand Surgery, University Hospital Zurich, 8091 Zurich, Switzerland.
Julia von AtzigenDepartment of Plastic Surgery and Hand Surgery, University Hospital Zurich, 8091 Zurich, Switzerland.
Roland BöniWhite House Center for Liposuction, 8044 Zurich, Switzerland.
Iris MiescherDepartment of Plastic Surgery and Hand Surgery, University Hospital Zurich, 8091 Zurich, Switzerland.ORCID 0000-0002-4448-8269
Pietro GiovanoliDepartment of Plastic Surgery and Hand Surgery, University Hospital Zurich, 8091 Zurich, Switzerland.
Maurizio CalcagniDepartment of Plastic Surgery and Hand Surgery, University Hospital Zurich, 8091 Zurich, Switzerland.ORCID 0000-0003-4372-0561
Maximilian Y EmmertInstitute for Regenerative Medicine (IREM), University of Zurich, 8952 Zurich, Switzerland.
Johanna BuschmannDivision of Surgical Research, University Hospital of Zurich, 8091 Zurich, Switzerland.ORCID 0000-0001-7919-7448

Funding

Hartmann-Müller Foundation, Zurich, Switzerland 1800Swiss National Science Foundation 310030_197578
6 · The paper itself

Abstract

Regeneration after ischemia requires to be promoted by (re)perfusion of the affected tissue, and, to date, there is no therapy that covers all needs. In treatment with mesenchymal stem cells (MSC), the secretome acts via paracrine mechanisms and has a positive influence on vascular regeneration via proangiogenic factors. A lack of standardization and the high complexity of vascular structures make it difficult to compare angiogenic readouts from different studies. This emphasizes the need for improved approaches and the introduction of an index in the preclinical setting. A characterization of human MSC secretomes obtained from one of the three formats-single cells, small, and large spheroids-was performed using the chicken aortic ring assay in combination with a modified angiogenic activity index (AAI) and an angiogenic profile. While the secretome of the small spheroid group showed an inhibitory effect on angiogenesis, the large spheroid group impressed with a fully pro-angiogenic response, and a higher AAI compared to the single cell group, underlying the suitability of these three-stem cell-derived secretomes with their distinct angiogenic properties to validate the AAI and the novel angiogenic profile established here.

Indexed as

AortaMesenchymal Stem CellsNeovascularization, PhysiologicAnimalsChickensHumansSpheroids, Cellularangiogenesisaortic ring assayindexmesenchymal stem cellssecretomespheroid

Identifiers

PMID39796147
PMCPMC11719671

What Socratic 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 Socratic graph.