Bone sialoprotein immobilized in collagen type I enhances angiogenesis in vitro and in ovo

dc.contributor.authorKriegel, Anja
dc.contributor.authorLangendorf, Eva
dc.contributor.authorKottmann, Valentina
dc.contributor.authorKämmerer, Peer W.
dc.contributor.authorArmbruster, Franz Paul
dc.contributor.authorWiesmann-Imilowski, Nadine
dc.contributor.authorBaranowski, Andreas
dc.contributor.authorGercek, Erol
dc.contributor.authorDrees, Philipp
dc.contributor.authorRommens, Pol Maria
dc.contributor.authorRitz, Ulrike
dc.date.accessioned2023-05-26T07:37:37Z
dc.date.available2023-05-26T07:37:37Z
dc.date.issued2023
dc.description.abstractBone fracture healing is a multistep process, including early immunological reactions, osteogenesis, and as a key factor, angiogenesis. Molecules inducing osteogenesis as well as angiogenesis are rare, but hold promise to be employed in bone tissue engineering. It has been demonstrated that the bone sialoprotein (BSP) can induce bone formation when immobilized in collagen type I, but its effect on angiogenesis still has to be characterized in detail. Therefore, the aim of this study was to analyse the effects of BSP immobilized in a collagen type I gel on angiogenesis. First, in vitro analyses with endothelial cells (HUVECs) were performed detecting enhancing effects of BSP on proliferation and gene expression of endothelial markers. A spheroid model was employed confirming these results. Finally, the inducing impact of BSP-collagen on vascular density was proved in a yolk sac membrane assay. Our results demonstrate that BSP is capable of inducing angiogenesis and confirm that collagen type I is the optimal carrier for this protein. Taking into account former results, and literature showing that BSP also induces osteogenesis, one can hypothesize that BSP couples angiogenesis and osteogenesis, making it a promising molecule to be used in bone tissue regeneration.en_GB
dc.description.sponsorshipDeutsche Forschungsgemeinschaft (DFG)|491381577|Open-Access-Publikationskosten 2022–2024 Universität Mainz - Universitätsmedizin
dc.identifier.doihttp://doi.org/10.25358/openscience-9123
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/9140
dc.language.isoeng
dc.rightsCC-BY-4.0
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 angiogenesis in vitro and in ovoen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.netprice1480,00
jgu.apc.price1583,60
jgu.apc.taxrate7
jgu.dfg.year2023
jgu.journal.issue4
jgu.journal.titlePolymers
jgu.journal.volume15
jgu.nationalcurrency.eur1480,00
jgu.organisation.departmentFB 04 Medizinde_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternative1007
jgu.publisher.doi10.3390/polym15041007
jgu.publisher.issn2073-4360
jgu.publisher.nameMDPI
jgu.publisher.placeBasel
jgu.publisher.year2023
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode610
jgu.subject.dfgNaturwissenschaftende_DE
jgu.type.contenttypeScientific articleen_GB
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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