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Tenocytic induction of stem cells from bone marrow on polymeric microparticles for a new concept of tendon regenerative prosthesis
dc.contributor.author | Claros-Gil, Silvia | |
dc.contributor.author | Araque-Monrós, Mª Carmen | |
dc.contributor.author | Rodríguez-Losada, Noela | |
dc.contributor.author | Gil-Santos, Luis | |
dc.contributor.author | Monleón-Pradas, Manuel | |
dc.contributor.author | Más-Estellés, Jorge | |
dc.contributor.author | Andrades-Gómez, José Antonio | |
dc.contributor.author | Becerra-Ratia, José | |
dc.date.accessioned | 2015-10-26T11:49:14Z | |
dc.date.available | 2015-10-26T11:49:14Z | |
dc.date.created | 2015 | |
dc.date.issued | 2015-10-26 | |
dc.identifier.uri | http://hdl.handle.net/10630/10593 | |
dc.description.abstract | A new concept of a regenerative and resorbable prosthesis for tendon and ligament has been developed. The prosthesis consists of a poly-lactide acid (PLA) braid, microparticles in its interior serving as cell carriers, and a surface non-adherent coating. The aim of this study is to select the most suitable support, microparticles of poly-L-lactide (PLLA) or chitosan (CHT), for carrying the cells inside the hollow PLA braid. Microparticles of these polymers were manufactured and blended with microparticles of hyaluronic acid (HA). All of them were physically and biologically characterized. Cell viability, morphology and proliferation of human mesenchymal stem cells (hMSCs) on the different supports were evaluated and compared, revealing that PLLA microparticles were the most appropriate to be used as injectable cell-carrier. Finally, hMSCs differentiation into tenocytes was carried out on PLLA microparticles using bone morphogenetic protein-12 (BMP-12) and a mixture of transforming growth factor-β1 (TGF-β1) and insulin-like growth factor1 (IGF-1). Cell morphology was analyzed by electronic and confocal microscopy and cell differentiation was evaluated immunocytochemically for the presence of type I collagen and tenomodulin. Besides, the tenomodulin and decorin gene expression were measured by real-time quantitative polymerase chain reaction (RT-qPCR). Our results showed that the medium supplemented with BMP-12 promoted higher expression of tenomodulin and decorin, both of them differentiation markers of tenocytes. This approach might be relevant to future tissue engineering applications in reconstruction of tendon and ligament defects. Authors acknowledge support of the Spanish Instituto de Salud Carlos III through CIBERbbn and the Spanish Network on Cell Therapy (Red TerCel) initiatives. | es_ES |
dc.description.sponsorship | Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech. | es_ES |
dc.language.iso | eng | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.subject | Materiales biomédicos | es_ES |
dc.subject.other | Tenocytes | es_ES |
dc.subject.other | Stem cells | es_ES |
dc.subject.other | Tendon regenerative | es_ES |
dc.subject.other | Biomaterials | es_ES |
dc.title | Tenocytic induction of stem cells from bone marrow on polymeric microparticles for a new concept of tendon regenerative prosthesis | es_ES |
dc.type | info:eu-repo/semantics/conferenceObject | es_ES |
dc.centro | Facultad de Ciencias | es_ES |
dc.relation.eventtitle | Sociedad Española de Terapia génica y celular | es_ES |
dc.relation.eventplace | San Sebastián | es_ES |
dc.relation.eventdate | Noviembre 2015 | es_ES |
dc.rights.cc | by-nc-nd |