Events1st Electronic Conference on Molecular Science
Published
This submission belongs to the session c. Stem Cells and Their Research Potential of the event 1st Electronic Conference on Molecular Science
Published date
13 Oct, 2015
Citation
Barbara Zavan, Amedo Carraro, Umberto Tedeschi, Chiara Gardin, Letizia Ferroni, Maurizio Buggio, Co-presence of Mesenchymal Stem Cells in an in vivo engineered liver pocket-scaffold increases neo-angiogenesis and albumin production, in Proceedings of 1st Electronic Conference on Molecular Science, 15 October–22 October 2015, MDPI: Basel, Switzerland, doi: 10.3390/ecms-1-c001
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Co-presence of Mesenchymal Stem Cells in an in vivo engineered liver pocket-scaffold increases neo-angiogenesis and albumin production

Amedo Carraro 1
Maurizio Buggio 2
Chiara Gardin 3
Umberto Tedeschi 1
Letizia Ferroni 3
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1. Department of General Surgery and Odontoiatrics, Liver Transplant Unit, University Hospital of Verona, P.le Aristide Stefani 1, 37126 Verona, Italy;
2. Inflammation and Repair The University of Manchester Manchester, United Kingdom
3. University of Padova, Dpt of Biomedical Sciences, Padova, Italy
Abstract

Introduction: Fabrication of three-dimensional (3D) liver tissue is limited by many factors, one of them is the lack of vascularization in the tissue-engineered constructs. To overcome these limitations, an in vivo engineered liver pocket-scaffold's ability to increase neo-angiogenesis was considered in the present study. Methods: Hyaluronan-besed scaffolds enriched with human Mesenchymal Stem Cells (hMSCs) and hepatocytes were implanted into rats. Angiogenesis and hepatocyte function were monitored. Results: The formation of de novo vascular networks within scaffolding matrices was noted as well as a better albumin production by the implanted hepatocytes. Conclusions: Our results emphasized that the presence in culture of hMSC increased tissue concentrations of growth factors and may promote angiogenesis resulting in a higher density of blood vessels coupled with a better metabolic support of hepatocytes.

Keywords
mesenchymal stem cell
neoangiogenesis
scaffold
liver tissue engineering
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