Publication:
An in vitro study of fibrin sealant as a carrier system for recombinant human bone morphogenetic protein (rhBMP)–9 for bone tissue engineering

cris.virtualsource.author-orcide0a928e9-880e-4c58-89bf-89503294c7cd
cris.virtualsource.author-orcid1393c5d0-5d9b-43a8-8954-60152d900db9
cris.virtualsource.author-orcida69924a4-d65b-4404-8a95-a2223709a37e
cris.virtualsource.author-orcid9f252f02-c021-498e-b353-703790b6d890
datacite.rightsrestricted
dc.contributor.authorKobayashi, Masako
dc.contributor.authorMottini, Matthias
dc.contributor.authorKobayashi, Eizaburo
dc.contributor.authorZhang, Yufeng
dc.contributor.authorSchaller, Benoît
dc.contributor.authorMiron, Richard John
dc.date.accessioned2024-12-13T15:40:42Z
dc.date.available2024-12-13T15:40:42Z
dc.date.issued2017-01
dc.description.abstractIn the craniofacial bone field, fibrin sealants are used as coagulant and adhesive tools to stabilize grafts during surgery. Despite this, their exact role in osteogenesis is poorly characterized. In the present study, we aimed to characterize the osteogenic potential of TISSEEL fibrin sealant and used its technology to incorporate growth factors within its matrix. We focused on recombinant human bone morphogenetic protein (rhBMP)-9, which has previously been characterized as one of the strongest osteogenetic inducers in the BMP family. TISSEEL displayed an excellent ability to retain rhBMP9, which was gradually released over a 10-day period. Although TISSEEL decreased bone stromal ST2 cell attachment at 8 h, it displayed normal cell proliferation at 1, 3, and 5 days when compared to tissue culture plastic. Interestingly, TISSEEL had little influence on osteoblast differentiation; however its combination with rhBMP9 significantly increased ALP activity at 7 days, Alizarin Red staining at 14 days, and mRNA levels of osteoblast differentiation markers ALP, bone sialoprotein, and osteocalcin. In summary, although fibrin sealants were shown to have little influence on osteogenesis, their combination with bone-inducing growth factors such as rhBMP9 may serve as an attractive carrier/scaffold for future bone regenerative strategies. Future animal studies are now necessary. Copyright © 2016 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved. KEYWORDS: BMP9; Bone morphogenetic proteins; Bone regeneration; Fibrin glue; Fibrin sealant; Osteogenesis
dc.description.numberOfPages6
dc.description.sponsorshipDepartement Klinische Forschung, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
dc.description.sponsorshipUniversitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
dc.identifier.doi10.7892/boris.95121
dc.identifier.pmid27840120
dc.identifier.publisherDOI10.1016/j.jcms.2016.10.008
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/192907
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofJournal of cranio-maxillo-facial surgery
dc.relation.issn1010-5182
dc.relation.organizationDCD5A442C54DE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C1F8E17DE0405C82790C4DE2
dc.subjectBMP9
dc.subjectBone morphogenetic proteins
dc.subjectBone regeneration
dc.subjectFibrin glue
dc.subjectFibrin sealant
dc.subjectOsteogenesis
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleAn in vitro study of fibrin sealant as a carrier system for recombinant human bone morphogenetic protein (rhBMP)–9 for bone tissue engineering
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage32
oaire.citation.issue1
oaire.citation.startPage27
oaire.citation.volume45
oairecerif.author.affiliationDepartement Klinische Forschung, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliationDepartement Klinische Forschung, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliationUniversitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliationDepartement Klinische Forschung, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliationUniversitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliation2Universitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliation2Universitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliation2Departement Klinische Forschung, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliation2Universitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
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unibe.description.ispublishedpub
unibe.eprints.legacyId95121
unibe.journal.abbrevTitleJ CRANIO MAXILL SURG
unibe.refereedtrue
unibe.subtype.articlejournal

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