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dc.contributor.authorCho, SW-
dc.contributor.authorPark, HJ-
dc.contributor.authorRyu, JH-
dc.contributor.authorKim, SH-
dc.contributor.authorKim, YH-
dc.contributor.authorChoi, CY-
dc.contributor.authorLee, MJ-
dc.contributor.authorKim, JS-
dc.contributor.authorJang, IS-
dc.contributor.authorKim, DI-
dc.contributor.authorKim, BS-
dc.date.accessioned2024-01-21T05:06:23Z-
dc.date.available2024-01-21T05:06:23Z-
dc.date.created2021-09-03-
dc.date.issued2005-05-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/136514-
dc.description.abstractSynthetic polymer vascular patches used in cardiovascular surgery have shortcomings such as thrombosis. intimal hyperplasia, calcification, infection, and no growth potential. Tissue-engineered vascular patches using autologous vascular cells may solve these problems. In this study, we developed a tissue-engineered vascular patch using autologous bone marrow-derived cells (BMCs) and decellularized tissue matrices. Vascular smooth muscle cells and endothelial cells were differentiated from bone mar-row mononuclear cells in vitro. Tissue-engineered vascular patches were fabricated by seeding these cells onto decellularized canine inferior vena cava matrices and implanted into the inferior vena cava of dogs. Three weeks after implantation. the tissue-engineered vascular patches were patent with no sign of thrombus formation. Histological, immunohistochemical, and electron microscopic analyses of the vascular patches retrieved 3 weeks after implantation revealed regeneration of endothelium and smooth muscle and the presence of collagen and elastin. BMCs labeled with a fluorescent dye prior to implantation were detected in the retrieved vascular patches, indicating that the BMCs survived after implantation and contributed to the vascular tissue regeneration. This study demonstrates that vascular patches can be tissue-engineered with autologous BMCs and decellularized tissue matrices. (C) 2004 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.subjectENDOTHELIAL PROGENITOR CELLS-
dc.subjectCAROTID-ENDARTERECTOMY-
dc.subjectEXTRACELLULAR-MATRIX-
dc.subjectSTROMAL CELLS-
dc.subjectIN-VIVO-
dc.subjectAUTOGRAFTS-
dc.subjectPOLYTETRAFLUOROETHYLENE-
dc.subjectNEOVASCULARIZATION-
dc.subjectDIFFERENTIATION-
dc.subjectIMMUNOGENICITY-
dc.titleVascular patches tissue-engineered with autologous bone marrow-derived cells and decellularized tissue matrices-
dc.typeArticle-
dc.identifier.doi10.1016/j.biomaterials.2004.06.018-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOMATERIALS, v.26, no.14, pp.1915 - 1924-
dc.citation.titleBIOMATERIALS-
dc.citation.volume26-
dc.citation.number14-
dc.citation.startPage1915-
dc.citation.endPage1924-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000226663800032-
dc.identifier.scopusid2-s2.0-20844432521-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusENDOTHELIAL PROGENITOR CELLS-
dc.subject.keywordPlusCAROTID-ENDARTERECTOMY-
dc.subject.keywordPlusEXTRACELLULAR-MATRIX-
dc.subject.keywordPlusSTROMAL CELLS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusAUTOGRAFTS-
dc.subject.keywordPlusPOLYTETRAFLUOROETHYLENE-
dc.subject.keywordPlusNEOVASCULARIZATION-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusIMMUNOGENICITY-
dc.subject.keywordAuthorvascular patch-
dc.subject.keywordAuthorbone marrow-derived cell-
dc.subject.keywordAuthordecellularized tissue matrix-
dc.subject.keywordAuthortissue engineering-
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