Abstract
| Lingua originale | English |
|---|---|
| pagine (da-a) | 11-20 |
| Numero di pagine | 10 |
| Rivista | Default journal |
| Volume | 47 |
| Stato di pubblicazione | Published - 2018 |
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All Science Journal Classification (ASJC) codes
- veterinary(all)
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Differentiation and characterization of rat adipose tissue mesenchymal stem cells into endothelial-like cells. / Purpari, Giuseppa; Cassata, Giovanni; Lo Monte, Attilio Ignazio; Damiano, Giuseppe; Altomare, Roberta; Palumbo, Vincenzo Davide; Cassata, Giovanni; Di Marco; Di Bella; Russotto; Santoro, Alessandra; Russo Lacerna; Gucciardi; Purpari, Giuseppa; Cannella; Piccione, Giuseppe; Guercio, Annalisa; Di Marco, Pietro.
In: Default journal, Vol. 47, 2018, pag. 11-20.Risultato della ricerca: Article
}
TY - JOUR
T1 - Differentiation and characterization of rat adipose tissue mesenchymal stem cells into endothelial-like cells
AU - Purpari, Giuseppa
AU - Cassata, Giovanni
AU - Lo Monte, Attilio Ignazio
AU - Damiano, Giuseppe
AU - Altomare, Roberta
AU - Palumbo, Vincenzo Davide
AU - Cassata, Giovanni
AU - Di Marco, null
AU - Di Bella, null
AU - Russotto, null
AU - Santoro, Alessandra
AU - Russo Lacerna, null
AU - Gucciardi, null
AU - Purpari, Giuseppa
AU - Cannella, null
AU - Piccione, Giuseppe
AU - Guercio, Annalisa
AU - Di Marco, Pietro
PY - 2018
Y1 - 2018
N2 - In this study, mesenchymal stem cells were isolated from rat adipose tissue (AD-MSCs) to characterize and differentiate them into endothelial-like cells. AD-MSCs were isolated by mechanical and enzymatic treatments, and their identity was verified by colony-forming units (CFU) test and by differentiation into cells of mesodermal lineages. The endothelial differentiation was induced by plating another aliquot of cells in EGM-2 medium, enriched with specific endothelial growth factors. Five subcultures were performed. The expression of stemness genes (OCT4, SOX2 and NANOG) was investigated. The presence of CD90 and the absence of the CD45 were evaluated by flow cytometry. The endothelial-like cells were characterized by the evaluation of morphological changes and gene expression analysis for endothelial markers (CD31, CD144, CD146). Characterization of AD-MSCs showed their ability to form clones, to differentiate in vitro and the OCT-4, SOX-2, NANOG genes expression. Immunophenotypic characterization showed the CD90 presence and the CD45 absence. The endothelial-like cells showed morphological changes, the expression of CD31, CD144, CD146 genes and the presence of CD31 membrane receptor. Matrigel assay showed their ability to form network and vessels-like structures. This study lays the foundations for future evaluation of the potential AD-MSCs pro-angiogenic and therapeutic role.
AB - In this study, mesenchymal stem cells were isolated from rat adipose tissue (AD-MSCs) to characterize and differentiate them into endothelial-like cells. AD-MSCs were isolated by mechanical and enzymatic treatments, and their identity was verified by colony-forming units (CFU) test and by differentiation into cells of mesodermal lineages. The endothelial differentiation was induced by plating another aliquot of cells in EGM-2 medium, enriched with specific endothelial growth factors. Five subcultures were performed. The expression of stemness genes (OCT4, SOX2 and NANOG) was investigated. The presence of CD90 and the absence of the CD45 were evaluated by flow cytometry. The endothelial-like cells were characterized by the evaluation of morphological changes and gene expression analysis for endothelial markers (CD31, CD144, CD146). Characterization of AD-MSCs showed their ability to form clones, to differentiate in vitro and the OCT-4, SOX-2, NANOG genes expression. Immunophenotypic characterization showed the CD90 presence and the CD45 absence. The endothelial-like cells showed morphological changes, the expression of CD31, CD144, CD146 genes and the presence of CD31 membrane receptor. Matrigel assay showed their ability to form network and vessels-like structures. This study lays the foundations for future evaluation of the potential AD-MSCs pro-angiogenic and therapeutic role.
UR - http://hdl.handle.net/10447/285679
M3 - Article
VL - 47
SP - 11
EP - 20
JO - Default journal
JF - Default journal
ER -