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In vitro osteogenic differentiation of marrow stromal cells encapsulated in biodegradable hydrogels

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dc.contributor.authorTemenoff, Johnna S.-
dc.contributor.authorPark, Hansoo-
dc.contributor.authorJabbari, Esmaiel-
dc.contributor.authorSheffield, Tiffany L.-
dc.contributor.authorLeBaron, Richard G.-
dc.contributor.authorAmbrose, Catherine G.-
dc.contributor.authorMikos, Antonios G.-
dc.date.available2020-08-07T03:20:20Z-
dc.date.issued2004-08-
dc.identifier.issn1549-3296-
dc.identifier.issn1552-4965-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/43079-
dc.description.abstractNovel hydrogel materials based on oligo(poly(ethylene glycol) fumarate) (OPF) crosslinked with a redox radical initiation system were recently developed in our laboratory as injectable cell carriers for orthopedic tissue engineering applications. The effect of OFF hydrogel material properties on in vitro osteogenic differentiation of encapsulated rat marrow stromal cells (MSCs) with and without the presence of osteogenic supplements (dexamethasone) was investigated. Two OFF formulations that resulted in hydrogels with different swelling properties were used to encapsulate rat MSCs (seeding density similar to13 million cells/ mL, samples 6 mm diameter X 0.5 mm thick before swelling) and osteogenic differentiation in these constructs over 28 days in vitro was determined via histology and biochemical assays for alkaline phosphatase, osteopontin and calcium. Evidence of MSC differentiation was apparent over the culture period for samples without dexamethasone, but there was large variability in calcium production between constructs using cells of the same source. Differentiation was also seen in samples cultured with osteogenic supplements, but calcium deposition varied depending on the source pool of MSCs. By day 28, osteopontin and calcium results suggested that, in the presence of dexamethasone, OPF hydrogels with greater swelling promoted embedded MSC differentiation over those that swelled less (43.7 +/- 16.5 mug calcium/sample and 16.4 +/- 2.8 mug calcium /sample, respectively). In histological sections, mineralized areas were apparent in all sample types many microns away from the cells. These experiments indicate that OFF hydrogels are promising materials for use as injectable MSC carriers and that hydrogel swelling properties can influence osteogenic differentiation of encapsulated progenitor cells. (C) 2004 Wiley Periodicals, Inc.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-
dc.titleIn vitro osteogenic differentiation of marrow stromal cells encapsulated in biodegradable hydrogels-
dc.typeArticle-
dc.identifier.doi10.1002/jbm.a.30064-
dc.identifier.bibliographicCitationJOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, v.70A, no.2, pp 235 - 244-
dc.description.isOpenAccessN-
dc.identifier.wosid000222673200009-
dc.identifier.scopusid2-s2.0-3342875552-
dc.citation.endPage244-
dc.citation.number2-
dc.citation.startPage235-
dc.citation.titleJOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A-
dc.citation.volume70A-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorthermal crosslinking-
dc.subject.keywordAuthorPEG-
dc.subject.keywordAuthorhydrogel-
dc.subject.keywordAuthormarrow stromal cells-
dc.subject.keywordAuthorcell encapsulation-
dc.subject.keywordAuthorcellular differentiation-
dc.subject.keywordAuthorbone tissue engineering-
dc.subject.keywordPlusGLYCOL) FUMARATE) HYDROGELS-
dc.subject.keywordPlusMESENCHYMAL STEM-CELLS-
dc.subject.keywordPlusBONE-MARROW-
dc.subject.keywordPlusPEG HYDROGELS-
dc.subject.keywordPlusCARTILAGE-
dc.subject.keywordPlusCHONDROCYTES-
dc.subject.keywordPlusCULTURE-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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