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Coating of human mesenchymal cells in 3D culture with bioinorganic nanoparticles promotes osteoblastic differentiation and gene transfection

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dc.contributor.author Gonzalez-McQuire, R en
dc.contributor.author Green, DW en
dc.contributor.author Partridge, KA en
dc.contributor.author Oreffo, ROC en
dc.contributor.author Mann, S en
dc.contributor.author Davis, SA en
dc.date.accessioned 2014-03-01T01:56:18Z
dc.date.available 2014-03-01T01:56:18Z
dc.date.issued 2007 en
dc.identifier.issn 09359648 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/28041
dc.subject.other Amino acids en
dc.subject.other Bone en
dc.subject.other Calcium phosphate en
dc.subject.other Coatings en
dc.subject.other Gene expression en
dc.subject.other Nanoparticles en
dc.subject.other Osteoblasts en
dc.subject.other Three dimensional en
dc.subject.other Bone matrix production en
dc.subject.other Differentiation en
dc.subject.other Surface coatings en
dc.subject.other Transfection en
dc.subject.other Cell culture en
dc.title Coating of human mesenchymal cells in 3D culture with bioinorganic nanoparticles promotes osteoblastic differentiation and gene transfection en
heal.type journalArticle en
heal.identifier.primary 10.1002/adma.200602770 en
heal.identifier.secondary http://dx.doi.org/10.1002/adma.200602770 en
heal.publicationDate 2007 en
heal.abstract Coating of human mesenchymal stem cells (MSC) in 3D culture with bioinorganic nanoparticles helps in promoting osteoblastic differentiation and gene transfection. Modifying human MSCs directly in aqueous suspension with surface coatings of amino acid-functionalized calcium phosphate nanoparticles offers new opportunities for preparing a range of osteoinductive hybrid 'living' biomaterials. This 3D coating strategy produces viable cell/hydroxyapatite (HAP) conjugates and plasmid DNA transfected constructs, by simple and efficient methods. The bioinorganic coating is sufficient to stimulate MSC differentiation and bone matrix production in the absence of osteogenic media. Furthermore, the incorporation of specific biomolecular stimuli in coated cell aggregates enhances gene expression compared to 2D methods involving adherent cells, and that this protocol is also applicable to primary human cells. en
heal.journalName Advanced Materials en
dc.identifier.doi 10.1002/adma.200602770 en
dc.identifier.volume 19 en
dc.identifier.issue 17 en
dc.identifier.spage 2236 en
dc.identifier.epage 2240 en


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