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

Wolint, Petra; Hofmann, Silvan; von Atzigen, Julia; Böni, Roland; Miescher, Iris; Giovanoli, Pietro; Calcagni, Maurizio; Emmert, Maximilian Y; Buschmann, Johanna (2024). Standardization to Characterize the Complexity of Vessel Network Using the Aortic Ring Model. International Journal of Molecular Sciences, 26(1):291.

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.

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > University Hospital Zurich > Clinic for Reconstructive Surgery
04 Faculty of Medicine > Institute for Regenerative Medicine (IREM)
Dewey Decimal Classification:610 Medicine & health
Language:English
Date:31 December 2024
Deposited On:08 Jan 2025 14:21
Last Modified:30 Jun 2025 02:06
Publisher:MDPI Publishing
ISSN:1422-0067
OA Status:Gold
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:https://doi.org/10.3390/ijms26010291
PubMed ID:39796147
Project Information:
  • Funder: FP7
  • Grant ID: 211800
  • Project Title: SBMPS - Structural Biology of Membrane Proteins
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  • Language: English
  • Licence: Creative Commons: Attribution 4.0 International (CC BY 4.0)

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