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dc.contributor.authorHong, Yu Jin-
dc.contributor.authorBae, Soon Eon-
dc.contributor.authorDo, Sun Hee-
dc.contributor.authorKim, Ik Hwan-
dc.contributor.authorHan, Dong Keun-
dc.contributor.authorPark, Kwideok-
dc.date.accessioned2024-01-20T16:04:17Z-
dc.date.available2024-01-20T16:04:17Z-
dc.date.created2021-09-05-
dc.date.issued2011-10-
dc.identifier.issn1598-5032-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/129923-
dc.description.abstractA cell-derived extracellular matrix (ECM) was naturally obtained and its effect on the induction of osteogenesis of bone marrow stromal cells (BMSCs) was investigated. Once porous composite scaffolds made of poly(L-lactic-co-glycolic acid) (PLGA), hydroxyapatite (HA), and beta-tricalcium phosphate (beta-TCP) were fabricated, these scaffolds were seeded with fibroblasts or preosteoblasts and cultured in vitro. They were then subjected to decellularization, resulting in fibroblasts-decellularized scaffolds (FDS) or preosteoblasts-decellularized scaffolds (PDS). Both fibronectin and type I collagen were clearly detected from the immunofluorescent staining of FDS and PDS, respectively. When the rabbit BMSCs-loaded scaffolds were cultured in the osteogenic medium for 4 weeks, the osteogenic potential of FDS and PDS was much greater than the PLGA/HA/beta-TCP (control), as identified by histological staining and the alkaline phosphatase (ALP) activity. Meanwhile, when BMSC-seeded FDS was implanted subcutaneously into the nude mice, the results also indicated more upregulated osteogenic differentiation of BMSCs in vivo compared to the control. This study suggests that the microenvironment created by cell-derived ECM can provide a favorable template in prompting the osteogenesis of BMSCs.-
dc.languageEnglish-
dc.publisherPOLYMER SOC KOREA-
dc.subjectMESENCHYMAL STEM-CELLS-
dc.subjectEXTRACELLULAR-MATRIX-
dc.subjectDIFFERENTIATION-
dc.subjectGROWTH-
dc.subjectHEART-
dc.titleDecellularized PLGA-based scaffolds and their osteogenic potential with bone marrow stromal cells-
dc.typeArticle-
dc.identifier.doi10.1007/s13233-011-1004-8-
dc.description.journalClass1-
dc.identifier.bibliographicCitationMACROMOLECULAR RESEARCH, v.19, no.10, pp.1090 - 1096-
dc.citation.titleMACROMOLECULAR RESEARCH-
dc.citation.volume19-
dc.citation.number10-
dc.citation.startPage1090-
dc.citation.endPage1096-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART001584611-
dc.identifier.wosid000294812500015-
dc.identifier.scopusid2-s2.0-80052651596-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.relation.journalResearchAreaPolymer Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusMESENCHYMAL STEM-CELLS-
dc.subject.keywordPlusEXTRACELLULAR-MATRIX-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusHEART-
dc.subject.keywordAuthorbone marrow stromal cells-
dc.subject.keywordAuthorosteogenic differentiation-
dc.subject.keywordAuthorextracellular matrix-
dc.subject.keywordAuthorscaffold-
dc.subject.keywordAuthordecellularization-
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KIST Article > 2011
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