Publication:
Comparison of the effects of recombinant human bone morphogenetic protein-2 and -9 on bone formation in rat calvarial critical-size defects.

cris.virtualsource.author-orcid9f252f02-c021-498e-b353-703790b6d890
cris.virtualsource.author-orciddac32003-dcbc-45b1-9c1e-d95ad19c43ce
datacite.rightsopen.access
dc.contributor.authorNakamura, Toshiaki
dc.contributor.authorShirakata, Yoshinori
dc.contributor.authorShinohara, Yukiya
dc.contributor.authorMiron, Richard John
dc.contributor.authorHasegawa-Nakamura, Kozue
dc.contributor.authorKobayashi, Masako
dc.contributor.authorNoguchi, Kazuyuki
dc.date.accessioned2024-10-25T13:52:07Z
dc.date.available2024-10-25T13:52:07Z
dc.date.issued2017-12
dc.description.abstractOBJECTIVES Among bone morphogenetic protein (BMP) family members, BMP-2 and BMP-9 have demonstrated potent osteoinductive potential. However, in vivo differences in their potential for bone regeneration remain unclear. The present study aimed to compare the effects of recombinant human (rh) BMP-2 and rhBMP-9 on bone formation in rat calvarial critical-size defects (CSD). MATERIALS AND METHODS Twenty-eight Wistar rats surgically received two calvarial defects bilaterally in each parietal bone. Defects (n = 56) were allocated into four groups: absorbable collagen sponge (ACS) alone, rhBMP-2 with ACS (rhBMP-2/ACS), rhBMP-9/ACS, or sham surgery (control), on the condition that the treatments of rhBMP-2/ACS and rhBMP-9/ACS, or the same treatments were not included in the same animal. Animals were sacrificed at 2 and 8 weeks post-surgery. The calvarial defects were analyzed for bone volume (BV) by micro-computed tomography and for percentages of defect closure (DC/DL), newly formed bone area (NBA/TA), bone marrow area (BMA/NBA), adipose tissue area (ATA/NBA), central bone height (CBH), and marginal bone height (MBH) by histomorphometric analysis. RESULTS The BV in the rhBMP-2/ACS group (5.44 ± 3.65 mm3, n = 7) was greater than the other groups at 2 weeks post-surgery, and the rhBMP-2/ACS and rhBMP-9/ACS groups (18.17 ± 2.51 and 16.30 ± 2.46 mm3, n = 7, respectively) demonstrated significantly greater amounts of BV compared with the control and ACS groups (6.02 ± 2.90 and 9.30 ± 2.75 mm3, n = 7, respectively) at 8 weeks post-surgery. The rhBMP-2/ACS and rhBMP-9/ACS groups significantly induced new bone formation compared to the control and ACS groups at 8 weeks post-surgery. However, there were no statistically significant differences found between the rhBMP-2/ACS and rhBMP-9/ACS groups in any of the histomorphometric parameters. The ATA/NBA in the rhBMP-2/ACS group (9.24 ± 3.72%, n = 7) was the highest among the treatment groups at 8 weeks post-surgery. CONCLUSIONS Within the limits of this study, it can be concluded that rhBMP-2/ACS induced a slight early increase in new bone formation at 2 weeks and that rhBMP-9/ACS provided comparable new bone formation to rhBMP-2/ACS with less adipose tissues after a healing period of 8 weeks in rat CSD. CLINICAL RELEVANCE RhBMP-9/ACS treatment provided new bone formation with less adipose tissues compared with rhBMP-2/ACS.
dc.description.numberOfPages9
dc.description.sponsorshipUniversitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
dc.description.sponsorshipDepartment for BioMedical Research, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
dc.identifier.doi10.7892/boris.111125
dc.identifier.pmid28197731
dc.identifier.publisherDOI10.1007/s00784-017-2069-3
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/158248
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofClinical oral investigations
dc.relation.issn1432-6981
dc.relation.organizationDCD5A442C54DE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C1F8E17DE0405C82790C4DE2
dc.subjectBone morphogenetic protein-2 Bone morphogenetic protein-9 Bone regeneration Collagen Growth factor
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleComparison of the effects of recombinant human bone morphogenetic protein-2 and -9 on bone formation in rat calvarial critical-size defects.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage2679
oaire.citation.issue9
oaire.citation.startPage2671
oaire.citation.volume21
oairecerif.author.affiliationUniversitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliationDepartment for BioMedical Research, Forschungsgruppe Schädel-, Kiefer- und Gesichtschirurgie
oairecerif.author.affiliation2Universitätsklinik für Schädel-, Kiefer- und Gesichtschirurgie
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.date.licenseChanged2019-10-23 02:22:09
unibe.description.ispublishedpub
unibe.eprints.legacyId111125
unibe.journal.abbrevTitleCLIN ORAL INVEST
unibe.refereedtrue
unibe.subtype.articlejournal

Files

Original bundle
Now showing 1 - 1 of 1
Name:
s00784-017-2069-3.pdf
Size:
1.34 MB
Format:
Adobe Portable Document Format
File Type:
text
License:
publisher
Content:
published

Collections