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Umbilical Cord Mesenchymal Stem Cell-Derived Nanovesicles Potentiate the Bone-Formation Efficacy of Bone Morphogenetic Protein 2

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dc.contributor.authorLim, Songhyun-
dc.contributor.authorLyu, Hao-Zhen-
dc.contributor.authorLee, Ju-Ro-
dc.contributor.authorHan, Shi Huan-
dc.contributor.authorLee, Jae Hyup-
dc.contributor.authorKim, Byung-Soo-
dc.date.accessioned2024-06-13T02:11:29Z-
dc.date.available2024-06-13T02:11:29Z-
dc.date.created2020-10-07-
dc.date.created2020-10-07-
dc.date.issued2020-09-
dc.identifier.citationInternational Journal of Molecular Sciences, Vol.21 No.17, pp.6425-16-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://hdl.handle.net/10371/204236-
dc.description.abstractRecombinant human bone morphogenetic protein 2 (rhBMP-2) is one of the most potent osteogenic factors used to treat bone loss. However, at higher doses, rhBMP-2 does not necessarily increase bone formation but rather increases the incidence of adverse side effects. Here, we investigated whether umbilical cord mesenchymal stem cell (UCMSC)-derived nanovesicles (NVs) further increase the in vivo bone formation at high doses of rhBMP-2. In the presence of UCMSC-derived NVs, proliferation, migration, and tube formation of human umbilical vein endothelial cells were stimulated in vitro. Furthermore, migration and osteogenesis of human bone marrow-derived mesenchymal stem cells were stimulated. To examine the efficacy of UCMSC-derived NVs on in vivo bone formation, collagen sponges soaked with rhBMP-2 and UCMSC-derived NVs were used in athymic nude mice with calvarial defects. At a high rhBMP-2 dosage (500 ng/mL), UCMSC-derived NVs significantly promoted bone formation in calvarial defects; however, the UCMSC-derived NVs alone did not induce in vivo bone formation. Our results indicate that UCMSC-derived NVs can potentiate the bone formation efficacy of rhBMP-2 at a high dosage.-
dc.language영어-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleUmbilical Cord Mesenchymal Stem Cell-Derived Nanovesicles Potentiate the Bone-Formation Efficacy of Bone Morphogenetic Protein 2-
dc.typeArticle-
dc.identifier.doi10.3390/ijms21176425-
dc.citation.journaltitleInternational Journal of Molecular Sciences-
dc.identifier.wosid000570382900001-
dc.identifier.scopusid2-s2.0-85090751303-
dc.citation.endpage16-
dc.citation.number17-
dc.citation.startpage6425-
dc.citation.volume21-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorLee, Jae Hyup-
dc.contributor.affiliatedAuthorKim, Byung-Soo-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusCOLLAGEN SPONGE-
dc.subject.keywordPlusDUAL DELIVERY-
dc.subject.keywordPlusPROMOTE ANGIOGENESIS-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusREGENERATION-
dc.subject.keywordPlusBMP-2-
dc.subject.keywordPlusEXOSOMES-
dc.subject.keywordPlusMICROVESICLES-
dc.subject.keywordPlusVEGF-
dc.subject.keywordAuthorrecombinant human bone morphogenetic protein 2-
dc.subject.keywordAuthorumbilical cord mesenchymal stem cell-derived nanovesicles-
dc.subject.keywordAuthorbone formation-
dc.subject.keywordAuthorangiogenesis-
dc.subject.keywordAuthorosteogenesis-
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area biomaterials, nanomedicine, regenerative medicine

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