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dc.contributor.authorChang, Yu-Jenen_US
dc.contributor.authorShih, Daniel Tzu-Bien_US
dc.contributor.authorTseng, Ching-Pingen_US
dc.contributor.authorHsieh, Tzu-Bouen_US
dc.contributor.authorLee, Don-Chingen_US
dc.contributor.authorHwang, Shiaw-Minen_US
dc.date.accessioned2014-12-08T15:17:14Z-
dc.date.available2014-12-08T15:17:14Z-
dc.date.issued2006-03-01en_US
dc.identifier.issn1066-5099en_US
dc.identifier.urihttp://dx.doi.org/10.1634/stemcells.2004-0308en_US
dc.identifier.urihttp://hdl.handle.net/11536/12565-
dc.description.abstractBone marrow and umbilical cord blood are reported to be the main sources of mesenchymal stem cells (MSCs), which have been proposed for many clinical applications. This study evaluated and quantitated the differentiation potential of bone marrow-derived MSCs (bmMSCs) and cord blood-derived MSCs (cbMSCs) by in vitro induction. Results indicated that cbMSCs had a significantly stronger osteogenic potential but lower capacity for adipogenic differentiation than bmMSCs. Leptin, an important regulator of mesenchymal differentiation, has a significantly stronger effect of promoting osteogenesis and inhibiting adipogenesis in bmMSCs than in cbMSCs. Moreover, Cbfa1 mRNA expression in bmMSCs and cbMSCs was affected to different degrees by leptin during osteogenesis. In contrast, leptin reduced PPAR gamma 2 mRNA expression to the same level during adipogenesis in both types of MSCs. These results demonstrate the disparate capacities of MSCs from bone marrow and cord blood and suggest that they be used differently in experimental and therapeutic studies. In addition, the disparate differentiation tendencies of MSCs from different sources should be considered in further applications.en_US
dc.language.isoen_USen_US
dc.subjectmesenchymal stem cellsen_US
dc.subjectdifferentiationen_US
dc.subjectleptinen_US
dc.titleDisparate mesenchyme-lineage tendencies in mesenchymal stem cells from human bone marrow and umbilical cord blooden_US
dc.typeArticleen_US
dc.identifier.doi10.1634/stemcells.2004-0308en_US
dc.identifier.journalSTEM CELLSen_US
dc.citation.volume24en_US
dc.citation.issue3en_US
dc.citation.spage679en_US
dc.citation.epage685en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000240636200023-
dc.citation.woscount111-
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