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Interfacing Sca-1pos Mesenchymal Stem Cells with Biocompatible Scaffolds with Different Chemical Composition and Geometry
被引:16
作者:
Forte, G.
[1
,2
]
Franzese, O.
[3
]
Pagliari, S.
[1
]
Pagliari, F.
[1
]
Di Francesco, A. M.
[4
]
Cossa, P.
[1
]
Laudisi, A.
[3
]
Fiaccavento, R.
[1
,2
]
Minieri, M.
[1
,2
]
Bonmassar, E.
[3
]
Di Nardo, P.
[1
,2
]
机构:
[1] Univ Roma Tor Vergata, Dipartimento Med Interna, Lab Cardiol Mol & Cellulare, I-00133 Rome, Italy
[2] INRC, I-40126 Bologna, Italy
[3] Univ Roma Tor Vergata, Dipartimento Neurosci, I-00133 Rome, Italy
[4] Univ Cattolica Sacro Cuore, Policlin Agostino Gemelli, Dipartimento Oncol Pediat, Rome, Italy
来源:
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY
|
2009年
关键词:
MARROW STROMAL CELLS;
BONE-MARROW;
TELOMERASE EXPRESSION;
LIFE-SPAN;
PROGENITOR CELLS;
PHOSPHORYLATION;
TRANSPLANTATION;
PROLIFERATION;
FIBROBLAST;
ACTIVATION;
D O I:
10.1155/2009/910610
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
An immortalized murine mesenchymal stem cell line (mTERT-MSC) enriched for Lin(neg)/Sca-1(pos) fraction has been obtained through the transfection of MSC with murine TERT and single-cell isolation. Such cell line maintained the typical MSC self-renewal capacity and continuously expressed MSC phenotype. Moreover, mTERT-MSC retained the functional features of freshly isolated MSC in culture without evidence of senescence or spontaneous differentiation events. Thus, mTERT-MSC have been cultured onto PLA films, 30 and 100 mu m PLA microbeads, and onto unpressed and pressed HYAFF-11 scaffolds. While the cells adhered preserving their morphology on PLA films, clusters of mTERT-MSC were detected on PLA beads and unpressed fibrous scaffolds. Finally, mTERT-MSC were not able to colonize the inner layers of pressed HYAFF-11. Nevertheless, such cell line displayed the ability to preserve Sca-1 expression and to retain multilineage potential when appropriately stimulated on all the scaffolds tested. Copyright (C) 2009
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