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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页数:10
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