Dynamic culture of osteogenic cells in biomimetically coated poly(caprolactone) nanofibre mesh constructs

dc.contributor.authorAraújo, J. V.
dc.contributor.authorReis, C. Cunha
dc.contributor.authorRada, Tommaso
dc.contributor.authorSilva, Marta Alves da
dc.contributor.authorGomes, Manuela E.
dc.contributor.authorYang, Y.
dc.contributor.authorAshammakhi, N.
dc.contributor.authorReis, R. L.
dc.contributor.authorEl-Haj, Alicia J.
dc.contributor.authorNeves, N. M.
dc.date.accessioned2012-11-05T11:33:34Z
dc.date.available2012-11-05T11:33:34Z
dc.date.issued2010
dc.description.abstractIn our previous work, biomimetic calcium phosphate-coated poly(caprolactone) nanofibre meshes (BCP-NMs) were demonstrated to be more effective for supporting cell attachment and proliferation under static conditions, when compared with poly(caprolactone) nanofibre meshes (PCL-NMs). In many applications, in vitro cultivation of constructs using bioreactors that support efficient nutrition of cells has appeared as an important step toward the development of functional grafts. This work aimed at studying the effects of dynamic culture conditions and biomimetic coating on bone cells grown on the nanofibre meshes. BCP-NM and PCL-NM were seeded with osteoblast-like cells (MG63--human osteosarcoma-derived cell line). The cell-seeded constructs were cultured within a rotating bioreactor that simulated microgravity, at a fixed rotating speed, for different time periods, and then characterized. Cell morphology, viability, and phenotype were assessed. PCL-NM constructs presented a higher number of dead cells than BCP-NM constructs. Under dynamic conditions, the production of proteins associated with the extracellular matrix of bone was higher on BCP-NM constructs than in the PCL-NM ones, which indicates that coated samples may provide cells with a better environment for tissue growth. It is suggested that improved mass transfer in the bioreactor in combination with the appropriate substrate were decisive factors for this highly positive outcome for generating bone.por
dc.description.sponsorshipThis work was developed under the scope of the EU Project Network of Excellence "Expertissues'' (NMP3-CT-2004-500283) and supported by Alea jacta est Marie Curie Actions (MEST-CT-2004-008104). M. Alves da Silva would like to acknowledge the Portuguese Foundation for Science and Technology for her grant (SFRH-BD-28708-2006). Jose V. Araujo is grateful to S. Rathbone, H. Sura, I. Wimpenny, I. Dublon, G. Jones, and E. D. Pinho for useful technical discussions.por
dc.distributioninternationalpor
dc.identifier.doi10.1089/ten.tea.2009.0223por
dc.identifier.issn1937-3341por
dc.identifier.issn1937-335Xpor
dc.identifier.pmid19728792por
dc.identifier.urihttps://hdl.handle.net/1822/20652
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherMary Ann Liebertpor
dc.rightsopenAccesspor
dc.subject.wosScience & Technologypor
dc.titleDynamic culture of osteogenic cells in biomimetically coated poly(caprolactone) nanofibre mesh constructspor
dc.typearticlepor
dspace.entity.typePublicationen
oaire.citationEndPage563por
oaire.citationIssue2por
oaire.citationStartPage557por
oaire.citationTitleTissue engineering. Part Apor
oaire.citationVolume16por
sdum.journalTissue engineering. Part Apor
sdum.publicationstatuspublishedpor

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