Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-8636
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dc.contributor.authorKriegel, Anja-
dc.contributor.authorSchlosser, Christian-
dc.contributor.authorHabeck, Tanja-
dc.contributor.authorDahmen, Christoph-
dc.contributor.authorGötz, Hermann-
dc.contributor.authorClauder, Franziska-
dc.contributor.authorArmbruster, Franz Paul-
dc.contributor.authorBaranowski, Andreas-
dc.contributor.authorDrees, Philipp-
dc.contributor.authorRommens, Pol Maria-
dc.contributor.authorRitz, Ulrike-
dc.date.accessioned2023-01-25T11:01:15Z-
dc.date.available2023-01-25T11:01:15Z-
dc.date.issued2022-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/8652-
dc.description.abstractThe use of bioactive molecules is a promising approach to enhance the bone healing properties of biomaterials. The aim of this study was to define the role of bone sialoprotein (BSP) immobilized in collagen type I in various settings. In vitro studies with human primary osteoblasts in mono- or in co-culture with endothelial cells demonstrated a slightly increased gene expression of osteogenic markers as well as an increased proliferation rate in osteoblasts after application of BSP immobilized in collagen type I. Two critical size bone defect models were used to analyze bone regeneration. BSP incorporated in collagen type I increased bone regeneration only marginally at one concentration in a calvarial defect model. To induce the mechanical stability, three-dimensional printing was used to produce a stable porous cylinder of polylactide. The cylinder was filled with collagen type I and immobilized BSP and implanted into a femoral defect of critical size in rats. This hybrid material was able to significantly induce bone regeneration. Our study clearly shows the osteogenic effect of BSP when combined with collagen type I as carrier and thereby offers various approaches and options for its use as bioactive molecule in bone substitute materials.en_GB
dc.description.sponsorshipGefördert durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491381577de
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleBone sialoprotein immobilized in collagen type I enhances bone regeneration in vitro and in vivoen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-8636-
jgu.type.contenttypeScientific articlede
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.number2700-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleInternational journal of bioprintingde
jgu.journal.volume8de
jgu.journal.issue3de
jgu.pages.alternative591de
jgu.publisher.year2022-
jgu.publisher.nameWhiocede
jgu.publisher.placeSingaporede
jgu.publisher.issn2424-8002de
jgu.organisation.placeMainz-
jgu.subject.ddccode610de
jgu.publisher.doi10.18063/ijb.v8i3.591de
jgu.organisation.rorhttps://ror.org/023b0x485-
jgu.subject.dfgLebenswissenschaftende
Appears in collections:DFG-491381577-G

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