Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/20334

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dc.contributor.authorEscobar Ivirico, J. L.-
dc.contributor.authorSalmerón-Sánchez, M.-
dc.contributor.authorGómez Ribelles, J. L.-
dc.contributor.authorMonleón Pradas, M.-
dc.contributor.authorSoria, Jose Miguel-
dc.contributor.authorGomes, Manuela E.-
dc.contributor.authorReis, R. L.-
dc.contributor.authorMano, J. F.-
dc.date.accessioned2012-09-24T14:10:49Z-
dc.date.available2012-09-24T14:10:49Z-
dc.date.issued2009-
dc.identifier.issn1552-4973por
dc.identifier.issn1552-4981por
dc.identifier.urihttps://hdl.handle.net/1822/20334-
dc.description.abstractWe have synthesized methacrylate-endcapped caprolactone networks with tailored water sorption ability, poly(CLMA-co-HEA), in the form of three-dimensional (3D) scaffolds with the same architecture but exhibiting different hydrophilicity character (xHEA50, 0.3, 0.5), and we investigated the interaction of goat bone marrow stromal cells (GBMSCs) with such structures. For this purpose, GBMSCs were seeded and cultured for 3, 7, 14, 21, and 28 days onto the developed scaffolds. Cells have proliferated throughout the whole scaffold volume. Cell adhesion and morphology were analyzed by SEM, whereas cell viability and proliferation was assessed by MTS test and DNA quantification concluding that numbers of cells increased as a function of the culturing time (until day 14) and also with the hydrophobic content in the samples (from 50 to 100% of CLMA). No significant difference between samples with 100% and 70% of CLMA were detected in some cases. Osteoblastic differentiation was followed by assessing the alkaline phosphatase activity of cells, as well as type I collagen and osteocalcin expressions levels until day 21. The three markers were positive at days 14 and 21 when cells were cultured in 100% CLMA substrates which suggests osteoblastic differentiation of mesenchymal stem cells within these scaffolds. On the other hand, when the CLMA content decreases (until 50%), type I collagen and osteocalcin were positive but ALP was negative indicating that the differentiation process is affected by hydrophilic content. We suggest that such system may be useful to extract information on the effect of materials’ wettability on the corresponding biological performance in a 3D environment. Such general insights may be relevant in the context of biomaterials selection for tissue engineering strategies.por
dc.description.sponsorshipContract grant sponsor: Spanish Ministry of Science Contract grant number: MAT2007-66759-C03-01por
dc.language.isoengpor
dc.publisherWileypor
dc.rightsopenAccesspor
dc.subjectMSCspor
dc.subjectStem cellspor
dc.subjectOsteogenic differentiationpor
dc.subjectCaprolactone 2-(methacryloyloxy) ethyl esterpor
dc.subjectCopolymerspor
dc.subjectScaffoldspor
dc.titleProliferation and differentiation of goat bone marrow stromal cells in 3d scaffolds with tunable hydrophilicitypor
dc.typearticlepor
dc.peerreviewedyespor
sdum.publicationstatuspublishedpor
oaire.citationStartPage277por
oaire.citationEndPage286por
oaire.citationIssue1por
oaire.citationTitleJournal of Biomedical Materials Research. Part B: Applied Biomaterialspor
oaire.citationVolume91Bpor
dc.identifier.doi10.1002/jbm.b.31400-
dc.identifier.pmid19441119por
dc.subject.wosScience & Technologypor
sdum.journalJournal of Biomedical Materials Research: Part Bpor
Aparece nas coleções:3B’s - Artigos em revistas/Papers in scientific journals

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