Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/112654
Campo DC Valoridioma
dc.contributor.authorTamaddon, Maryamen_US
dc.contributor.authorBlunn, Gordonen_US
dc.contributor.authorXu, Weien_US
dc.contributor.authorAlemán Domínguez, María Elenaen_US
dc.contributor.authorMonzón, Marioen_US
dc.contributor.authorDonaldson, Jamesen_US
dc.contributor.authorSkinner, Johnen_US
dc.contributor.authorArnett, Timothy R.en_US
dc.contributor.authorWang, Lingen_US
dc.contributor.authorLiu, Chaozongen_US
dc.date.accessioned2021-11-15T14:33:10Z-
dc.date.available2021-11-15T14:33:10Z-
dc.date.issued2021en_US
dc.identifier.otherScopus-
dc.identifier.urihttp://hdl.handle.net/10553/112654-
dc.description.abstractAims Minimally manipulated cells, such as autologous bone marrow concentrates (BMC), have been investigated in orthopaedics as both a primary therapeutic and augmentation to existing restoration procedures. However, the efficacy of BMC in combination with tissue engineering is still unclear. In this study, we aimed to determine whether the addition of BMC to an osteochondral scaffold is safe and can improve the repair of large osteochondral defects when compared to the scaffold alone. Methods The ovine femoral condyle model was used. Bone marrow was aspirated, concentrated, and used intraoperatively with a collagen/hydroxyapatite scaffold to fill the osteochondral defects (n = 6). Tissue regeneration was then assessed versus the scaffold-only group (n = 6). Histological staining of cartilage with alcian blue and safranin-O, changes in chondrogenic gene expression, microCT, peripheral quantitative CT (pQCT), and force-plate gait analyses were performed. Lymph nodes and blood were analyzed for safety. Results The results six months postoperatively showed that there were no significant differences in bone regrowth and mineral density between BMC-treated animals and controls. A significant upregulation of messenger RNA (mRNA) for types I and II collagens in the BMC group was observed, but there were no differences in the formation of hyaline-like cartilage between the groups. A trend towards reduced sulphated glycosaminoglycans (sGAG) breakdown was detected in the BMC group but this was not statistically significant. Functional weightbearing was not affected by the inclusion of BMC. Conclusion Our results indicated that the addition of BMC to scaffold is safe and has some potentially beneficial effects on osteochondral-tissue regeneration, but not on the functional endpoint of orthopaedic interest.en_US
dc.languageengen_US
dc.relation.ispartofBone and Joint Researchen_US
dc.sourceBone and Joint Research[EISSN 2046-3758],v. 10 (10), p. 677-689, (Octubre 2021)en_US
dc.subject3313 Tecnología e ingeniería mecánicasen_US
dc.subject.otherBone Marrow Concentrateen_US
dc.subject.otherMinimally Manipulated Cellsen_US
dc.subject.otherOsteochondral Scaffolden_US
dc.titleSheep condyle model evaluation of bone marrow cell concentrate combined with a scaffold for repair of large osteochondral defectsen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1302/2046-3758.1010.BJR-2020-0504.R1en_US
dc.identifier.scopus85118394251-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.authorscopusid55581409800-
dc.contributor.authorscopusid7004735871-
dc.contributor.authorscopusid57320921200-
dc.contributor.authorscopusid56097219900-
dc.contributor.authorscopusid7003371153-
dc.contributor.authorscopusid35760297500-
dc.contributor.authorscopusid8281611700-
dc.contributor.authorscopusid7003686898-
dc.contributor.authorscopusid57034587600-
dc.contributor.authorscopusid57188879979-
dc.identifier.eissn2046-3758-
dc.description.lastpage689en_US
dc.identifier.issue10-
dc.description.firstpage677en_US
dc.relation.volume10en_US
dc.investigacionIngeniería y Arquitecturaen_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.date.coverdateOctubre 2021en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-INGen_US
dc.description.sjr1,268
dc.description.jcr4,41
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptGIR Fabricación integrada y avanzada-
crisitem.author.deptGIR Fabricación integrada y avanzada-
crisitem.author.deptDepartamento de Ingeniería Mecánica-
crisitem.author.orcid0000-0002-2254-9905-
crisitem.author.orcid0000-0003-2736-7905-
crisitem.author.parentorgDepartamento de Ingeniería Mecánica-
crisitem.author.parentorgDepartamento de Ingeniería Mecánica-
crisitem.author.fullNameAleman Dominguez,Maria Elena-
crisitem.author.fullNameMonzón Verona, Mario Domingo-
Colección:Artículos
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