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dc.contributor.authorCho, CS-
dc.contributor.authorSeo, SJ-
dc.contributor.authorPark, IK-
dc.contributor.authorKim, SH-
dc.contributor.authorKim, TH-
dc.contributor.authorHoshiba, T-
dc.contributor.authorHarada, I-
dc.contributor.authorAkaike, T-
dc.date.accessioned2024-01-21T03:40:14Z-
dc.date.available2024-01-21T03:40:14Z-
dc.date.created2021-09-01-
dc.date.issued2006-02-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/135799-
dc.description.abstractExtracellular matrix (ECM) plays important roles in tissue engineering because cellular growth and differentiation, in the two-dimensional cell culture as well as in the three-dimensional space of the developing organism, require ECM with which the cells can interact. Especially, the bioartificial liver-assist device or regeneration of the liver-tissue substitutes for liver tissue engineering requires a suitable ECM for hepatocyte culture because hepatocytes are anchorage-dependent cells and are highly sensitive to the ECM milieu for the maintenance of their viability and differentiated functions. Galactose-carrying synthetic ECMs derived from synthetic polymers and natural polymers bind hepatocytes through a receptor-mediated mechanism, resulting in enhanced hepatocyte functions. Attachment and functions of hepatocytes were affected by physico-chemical properties including ECM geometry as well as the type, density and orientation of galactose. Also, cellular environment, medium composition and dynamic culture system influenced liver-specific functions of hepatocytes beside ECM. (c) 2005 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.subjectADULT-RAT HEPATOCYTES-
dc.subjectLONG-TERM CULTURE-
dc.subjectPRIMARY MONOLAYER-CULTURES-
dc.subjectDIFFERENTIATED FUNCTIONS-
dc.subjectCELL-CELL-
dc.subjectASIALOGLYCOPROTEIN RECEPTORS-
dc.subjectSANDWICH CONFIGURATION-
dc.subjectBIODEGRADABLE POLYMERS-
dc.subjectALGINATE SCAFFOLDS-
dc.subjectFLOW BIOREACTOR-
dc.titleGalactose-carrying polymers as extracellular matrices for liver tissue engineering-
dc.typeArticle-
dc.identifier.doi10.1016/j.biomaterials.2005.06.008-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOMATERIALS, v.27, no.4, pp.576 - 585-
dc.citation.titleBIOMATERIALS-
dc.citation.volume27-
dc.citation.number4-
dc.citation.startPage576-
dc.citation.endPage585-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000233450400005-
dc.identifier.scopusid2-s2.0-26844525463-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeReview-
dc.subject.keywordPlusADULT-RAT HEPATOCYTES-
dc.subject.keywordPlusLONG-TERM CULTURE-
dc.subject.keywordPlusPRIMARY MONOLAYER-CULTURES-
dc.subject.keywordPlusDIFFERENTIATED FUNCTIONS-
dc.subject.keywordPlusCELL-CELL-
dc.subject.keywordPlusASIALOGLYCOPROTEIN RECEPTORS-
dc.subject.keywordPlusSANDWICH CONFIGURATION-
dc.subject.keywordPlusBIODEGRADABLE POLYMERS-
dc.subject.keywordPlusALGINATE SCAFFOLDS-
dc.subject.keywordPlusFLOW BIOREACTOR-
dc.subject.keywordAuthorgalactose-
dc.subject.keywordAuthorextracellular matrix-
dc.subject.keywordAuthorhepatocyte-
dc.subject.keywordAuthortissue engineering-
dc.subject.keywordAuthorasialoglycoprotein receptors-
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