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Electrospun PLLA nanofiber scaffolds and their use in combination with BMP-2 for reconstruction of bone defects

cris.virtual.author-orcid0000-0002-5416-6650
cris.virtualsource.author-orcid036bba9b-5ebe-4168-a978-4a56bde35a9b
datacite.rightsopen.access
dc.contributor.authorSchofer, Markus D.
dc.contributor.authorRoessler, Philip P.
dc.contributor.authorSchaefer, Jan
dc.contributor.authorTheisen, Christina
dc.contributor.authorSchlimme, Sonja
dc.contributor.authorHeverhagen, Johannes
dc.contributor.authorVoelker, Maximilian
dc.contributor.authorDersch, Roland
dc.contributor.authorAgarwal, Seema
dc.contributor.authorFuchs-Winkelmann, Susanne
dc.contributor.authorPaletta, Jürgen R. J.
dc.date.accessioned2024-10-11T09:25:54Z
dc.date.available2024-10-11T09:25:54Z
dc.date.issued2011
dc.description.abstractIntroduction Adequate migration and differentiation of mesenchymal stem cells is essential for regeneration of large bone defects. To achieve this, modern graft materials are becoming increasingly important. Among them, electrospun nanofiber scaffolds are a promising approach, because of their high physical porosity and potential to mimic the extracellular matrix (ECM). Materials and Methods The objective of the present study was to examine the impact of electrospun PLLA nanofiber scaffolds on bone formation in vivo, using a critical size rat calvarial defect model. In addition we analyzed whether direct incorporation of bone morphogenetic protein 2 (BMP-2) into nanofibers could enhance the osteoinductivity of the scaffolds. Two critical size calvarial defects (5 mm) were created in the parietal bones of adult male Sprague-Dawley rats. Defects were either (1) left unfilled, or treated with (2) bovine spongiosa, (3) PLLA scaffolds alone or (4) PLLA/BMP-2 scaffolds. Cranial CT-scans were taken at fixed intervals in vivo. Specimens obtained after euthanasia were processed for histology, histomorphometry and immunostaining (Osteocalcin, BMP-2 and Smad5). Results PLLA scaffolds were well colonized with cells after implantation, but only showed marginal ossification. PLLA/BMP-2 scaffolds showed much better bone regeneration and several ossification foci were observed throughout the defect. PLLA/BMP-2 scaffolds also stimulated significantly faster bone regeneration during the first eight weeks compared to bovine spongiosa. However, no significant differences between these two scaffolds could be observed after twelve weeks. Expression of osteogenic marker proteins in PLLA/BMP-2 scaffolds continuously increased throughout the observation period. After twelve weeks osteocalcin, BMP-2 and Smad5 were all significantly higher in the PLLA/BMP-2 group than in all other groups. Conclusion Electrospun PLLA nanofibers facilitate colonization of bone defects, while their use in combination with BMP-2 also increases bone regeneration in vivo and thus combines osteoconductivity of the scaffold with the ability to maintain an adequate osteogenic stimulus.
dc.description.numberOfPages1
dc.description.sponsorshipInstitut für Diagnostische, Interventionelle und Pädiatrische Radiologie
dc.identifier.doi10.7892/boris.7654
dc.identifier.isi000295936900068
dc.identifier.pmid21980467
dc.identifier.publisherDOI10.1371/journal.pone.0025462
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/78105
dc.language.isoen
dc.publisherPublic Library of Science
dc.publisher.placeLawrence, Kans.
dc.relation.ispartofPLoS ONE
dc.relation.issn1932-6203
dc.relation.organizationInstitute of Diagnostic, Interventional and Paediatric Radiology
dc.titleElectrospun PLLA nanofiber scaffolds and their use in combination with BMP-2 for reconstruction of bone defects
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue9
oaire.citation.startPagee25462
oaire.citation.volume6
oairecerif.author.affiliationInstitut für Diagnostische, Interventionelle und Pädiatrische Radiologie
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unibe.description.ispublishedpub
unibe.eprints.legacyId7654
unibe.journal.abbrevTitlePLOS ONE
unibe.refereedtrue
unibe.subtype.articlejournal

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