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Simple and Rapid Non-Enzymatic Procedure Allows the Isolation of Structurally Preserved Connective Tissue Micro-Fragments Enriched with SVF

The stromal vascular fraction (SVF) consists of a heterogeneous population of stem and stromal cells, generally obtained from adipose tissue by enzymatic digestion. For human cell-based therapies, mechanical process methods to obtain SVF represent an advantageous approach because they have fewer reg...

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Autores principales: Busato, Alice, De Francesco, Francesco, Biswas, Reetuparna, Mannucci, Silvia, Conti, Giamaica, Fracasso, Giulio, Conti, Anita, Riccio, Valentina, Riccio, Michele, Sbarbati, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824313/
https://www.ncbi.nlm.nih.gov/pubmed/33383682
http://dx.doi.org/10.3390/cells10010036
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author Busato, Alice
De Francesco, Francesco
Biswas, Reetuparna
Mannucci, Silvia
Conti, Giamaica
Fracasso, Giulio
Conti, Anita
Riccio, Valentina
Riccio, Michele
Sbarbati, Andrea
author_facet Busato, Alice
De Francesco, Francesco
Biswas, Reetuparna
Mannucci, Silvia
Conti, Giamaica
Fracasso, Giulio
Conti, Anita
Riccio, Valentina
Riccio, Michele
Sbarbati, Andrea
author_sort Busato, Alice
collection PubMed
description The stromal vascular fraction (SVF) consists of a heterogeneous population of stem and stromal cells, generally obtained from adipose tissue by enzymatic digestion. For human cell-based therapies, mechanical process methods to obtain SVF represent an advantageous approach because they have fewer regulatory restrictions for their clinical use. The aim of this study was to characterize a novel commercial system for obtaining SVF from adipose tissue by a mechanical approach without substantial manipulations. Lipoaspirate samples collected from 27 informed patients were processed by a simple and fast mechanical system (by means of Hy-Tissue SVF). The Hy-Tissue SVF product contained a free cell fraction and micro-fragments of stromal connective tissue. The enzymatic digestion of the micro-fragments increased the yield of free cells (3.2 times) and CFU-F (2.4 times). Additionally, 10% of free cells from SVF were positive for CD34+, suggesting the presence of endothelial cells, pericytes, and potential adipose-derived stem cells (ADSC). Moreover, the SVF cells were able to proliferate and differentiate in vitro toward adipocytes, osteocytes, and chondrocytes. The immunophenotypic analysis of expanded cells showed positivity for typical mesenchymal stem cell markers. The Hy-Tissue SVF system allows the isolation of stromal vascular fraction, making this product of potential interest in regenerative medicine.
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spelling pubmed-78243132021-01-24 Simple and Rapid Non-Enzymatic Procedure Allows the Isolation of Structurally Preserved Connective Tissue Micro-Fragments Enriched with SVF Busato, Alice De Francesco, Francesco Biswas, Reetuparna Mannucci, Silvia Conti, Giamaica Fracasso, Giulio Conti, Anita Riccio, Valentina Riccio, Michele Sbarbati, Andrea Cells Article The stromal vascular fraction (SVF) consists of a heterogeneous population of stem and stromal cells, generally obtained from adipose tissue by enzymatic digestion. For human cell-based therapies, mechanical process methods to obtain SVF represent an advantageous approach because they have fewer regulatory restrictions for their clinical use. The aim of this study was to characterize a novel commercial system for obtaining SVF from adipose tissue by a mechanical approach without substantial manipulations. Lipoaspirate samples collected from 27 informed patients were processed by a simple and fast mechanical system (by means of Hy-Tissue SVF). The Hy-Tissue SVF product contained a free cell fraction and micro-fragments of stromal connective tissue. The enzymatic digestion of the micro-fragments increased the yield of free cells (3.2 times) and CFU-F (2.4 times). Additionally, 10% of free cells from SVF were positive for CD34+, suggesting the presence of endothelial cells, pericytes, and potential adipose-derived stem cells (ADSC). Moreover, the SVF cells were able to proliferate and differentiate in vitro toward adipocytes, osteocytes, and chondrocytes. The immunophenotypic analysis of expanded cells showed positivity for typical mesenchymal stem cell markers. The Hy-Tissue SVF system allows the isolation of stromal vascular fraction, making this product of potential interest in regenerative medicine. MDPI 2020-12-29 /pmc/articles/PMC7824313/ /pubmed/33383682 http://dx.doi.org/10.3390/cells10010036 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Busato, Alice
De Francesco, Francesco
Biswas, Reetuparna
Mannucci, Silvia
Conti, Giamaica
Fracasso, Giulio
Conti, Anita
Riccio, Valentina
Riccio, Michele
Sbarbati, Andrea
Simple and Rapid Non-Enzymatic Procedure Allows the Isolation of Structurally Preserved Connective Tissue Micro-Fragments Enriched with SVF
title Simple and Rapid Non-Enzymatic Procedure Allows the Isolation of Structurally Preserved Connective Tissue Micro-Fragments Enriched with SVF
title_full Simple and Rapid Non-Enzymatic Procedure Allows the Isolation of Structurally Preserved Connective Tissue Micro-Fragments Enriched with SVF
title_fullStr Simple and Rapid Non-Enzymatic Procedure Allows the Isolation of Structurally Preserved Connective Tissue Micro-Fragments Enriched with SVF
title_full_unstemmed Simple and Rapid Non-Enzymatic Procedure Allows the Isolation of Structurally Preserved Connective Tissue Micro-Fragments Enriched with SVF
title_short Simple and Rapid Non-Enzymatic Procedure Allows the Isolation of Structurally Preserved Connective Tissue Micro-Fragments Enriched with SVF
title_sort simple and rapid non-enzymatic procedure allows the isolation of structurally preserved connective tissue micro-fragments enriched with svf
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824313/
https://www.ncbi.nlm.nih.gov/pubmed/33383682
http://dx.doi.org/10.3390/cells10010036
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