Interfacing Sca-1pos Mesenchymal Stem Cells with Biocompatible Scaffolds with Different Chemical Composition and Geometry

An immortalized murine mesenchymal stem cell line (mTERT-MSC) enriched for Linneg/Sca-1pos 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....

Full description

Bibliographic Details
Main Authors: G. Forte, O. Franzese, S. Pagliari, F. Pagliari, A. M. Di Francesco, P. Cossa, A. Laudisi, R. Fiaccavento, M. Minieri, E. Bonmassar, P. Di Nardo
Format: Article
Language:English
Published: Hindawi Limited 2009-01-01
Series:Journal of Biomedicine and Biotechnology
Online Access:http://dx.doi.org/10.1155/2009/910610
id doaj-c22645e424e94f23ae39480618ec411f
record_format Article
spelling doaj-c22645e424e94f23ae39480618ec411f2020-11-24T21:49:52ZengHindawi LimitedJournal of Biomedicine and Biotechnology1110-72431110-72512009-01-01200910.1155/2009/910610910610Interfacing Sca-1pos Mesenchymal Stem Cells with Biocompatible Scaffolds with Different Chemical Composition and GeometryG. Forte0O. Franzese1S. Pagliari2F. Pagliari3A. M. Di Francesco4P. Cossa5A. Laudisi6R. Fiaccavento7M. Minieri8E. Bonmassar9P. Di Nardo10Laboratorio di Cardiologia Molecolare e Cellulare, Dipartimento di Medicina Interna, Università di Roma “Tor Vergata”, 00133 Roma, ItalyDipartimento di Neuroscienze, Università di Roma “Tor Vergata”, 00133 Roma, ItalyLaboratorio di Cardiologia Molecolare e Cellulare, Dipartimento di Medicina Interna, Università di Roma “Tor Vergata”, 00133 Roma, ItalyLaboratorio di Cardiologia Molecolare e Cellulare, Dipartimento di Medicina Interna, Università di Roma “Tor Vergata”, 00133 Roma, ItalyDipartimento di Oncologia Pediatrica, Policlinico Agostino Gemelli, Università Cattolica del Sacro Cuore, Roma, ItalyLaboratorio di Cardiologia Molecolare e Cellulare, Dipartimento di Medicina Interna, Università di Roma “Tor Vergata”, 00133 Roma, ItalyDipartimento di Neuroscienze, Università di Roma “Tor Vergata”, 00133 Roma, ItalyLaboratorio di Cardiologia Molecolare e Cellulare, Dipartimento di Medicina Interna, Università di Roma “Tor Vergata”, 00133 Roma, ItalyLaboratorio di Cardiologia Molecolare e Cellulare, Dipartimento di Medicina Interna, Università di Roma “Tor Vergata”, 00133 Roma, ItalyDipartimento di Neuroscienze, Università di Roma “Tor Vergata”, 00133 Roma, ItalyLaboratorio di Cardiologia Molecolare e Cellulare, Dipartimento di Medicina Interna, Università di Roma “Tor Vergata”, 00133 Roma, ItalyAn immortalized murine mesenchymal stem cell line (mTERT-MSC) enriched for Linneg/Sca-1pos 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 μm 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.http://dx.doi.org/10.1155/2009/910610
collection DOAJ
language English
format Article
sources DOAJ
author G. Forte
O. Franzese
S. Pagliari
F. Pagliari
A. M. Di Francesco
P. Cossa
A. Laudisi
R. Fiaccavento
M. Minieri
E. Bonmassar
P. Di Nardo
spellingShingle G. Forte
O. Franzese
S. Pagliari
F. Pagliari
A. M. Di Francesco
P. Cossa
A. Laudisi
R. Fiaccavento
M. Minieri
E. Bonmassar
P. Di Nardo
Interfacing Sca-1pos Mesenchymal Stem Cells with Biocompatible Scaffolds with Different Chemical Composition and Geometry
Journal of Biomedicine and Biotechnology
author_facet G. Forte
O. Franzese
S. Pagliari
F. Pagliari
A. M. Di Francesco
P. Cossa
A. Laudisi
R. Fiaccavento
M. Minieri
E. Bonmassar
P. Di Nardo
author_sort G. Forte
title Interfacing Sca-1pos Mesenchymal Stem Cells with Biocompatible Scaffolds with Different Chemical Composition and Geometry
title_short Interfacing Sca-1pos Mesenchymal Stem Cells with Biocompatible Scaffolds with Different Chemical Composition and Geometry
title_full Interfacing Sca-1pos Mesenchymal Stem Cells with Biocompatible Scaffolds with Different Chemical Composition and Geometry
title_fullStr Interfacing Sca-1pos Mesenchymal Stem Cells with Biocompatible Scaffolds with Different Chemical Composition and Geometry
title_full_unstemmed Interfacing Sca-1pos Mesenchymal Stem Cells with Biocompatible Scaffolds with Different Chemical Composition and Geometry
title_sort interfacing sca-1pos mesenchymal stem cells with biocompatible scaffolds with different chemical composition and geometry
publisher Hindawi Limited
series Journal of Biomedicine and Biotechnology
issn 1110-7243
1110-7251
publishDate 2009-01-01
description An immortalized murine mesenchymal stem cell line (mTERT-MSC) enriched for Linneg/Sca-1pos 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 μm 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.
url http://dx.doi.org/10.1155/2009/910610
work_keys_str_mv AT gforte interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT ofranzese interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT spagliari interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT fpagliari interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT amdifrancesco interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT pcossa interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT alaudisi interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT rfiaccavento interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT mminieri interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT ebonmassar interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
AT pdinardo interfacingsca1posmesenchymalstemcellswithbiocompatiblescaffoldswithdifferentchemicalcompositionandgeometry
_version_ 1725886902172647424