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dc.contributor.authorLee, Soojin-
dc.contributor.authorLee, Hyun Su-
dc.contributor.authorChung, Justin J.-
dc.contributor.authorKim, Soo Hyun-
dc.contributor.authorPark, Jong Woong-
dc.contributor.authorLee, Kangwon-
dc.contributor.authorJung, Youngmee-
dc.date.accessioned2024-01-19T15:05:25Z-
dc.date.available2024-01-19T15:05:25Z-
dc.date.created2021-09-05-
dc.date.issued2021-03-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/117328-
dc.description.abstractA flexible and bioactive scaffold for adipose tissue engineering was fabricated and evaluated by dual nozzle three-dimensional printing. A highly elastic poly (L-lactide-co-epsilon-caprolactone) (PLCL) copolymer, which acted as the main scaffolding, and human adipose tissue derived decellularized extracellular matrix (dECM) hydrogels were used as the printing inks to form the scaffolds. To prepare the three-dimensional (3D) scaffolds, the PLCL co-polymer was printed with a hot melting extruder system while retaining its physical character, similar to adipose tissue, which is beneficial for regeneration. Moreover, to promote adipogenic differentiation and angiogenesis, adipose tissue-derived dECM was used. To optimize the printability of the hydrogel inks, a mixture of collagen type I and dECM hydrogels was used. Furthermore, we examined the adipose tissue formation and angiogenesis of the PLCL/dECM complex scaffold. From in vivo experiments, it was observed that the matured adipose-like tissue structures were abundant, and the number of matured capillaries was remarkably higher in the hydrogel-PLCL group than in the PLCL-only group. Moreover, a higher expression of M2 macrophages, which are known to be involved in the remodeling and regeneration of tissues, was detected in the hydrogel-PLCL group by immunofluorescence analysis. Based on these results, we suggest that our PLCL/dECM fabricated by a dual 3D printing system will be useful for the treatment of large volume fat tissue regeneration.-
dc.languageEnglish-
dc.publisherMDPI-
dc.subjectSMALL-INTESTINAL SUBMUCOSA-
dc.subjectMESENCHYMAL STEM-CELLS-
dc.subjectPOROUS SCAFFOLD DESIGN-
dc.subjectEXTRACELLULAR-MATRIX-
dc.subjectDEGRADATION BEHAVIOR-
dc.subjectIN-VITRO-
dc.subjectBIOMATERIAL-
dc.subjectBONE-
dc.subjectINFLAMMATION-
dc.subjectANGIOGENESIS-
dc.titleEnhanced Regeneration of Vascularized Adipose Tissue with Dual 3D-Printed Elastic Polymer/dECM Hydrogel Complex-
dc.typeArticle-
dc.identifier.doi10.3390/ijms22062886-
dc.description.journalClass1-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.22, no.6, pp.1 - 22-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.volume22-
dc.citation.number6-
dc.citation.startPage1-
dc.citation.endPage22-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000645698100001-
dc.identifier.scopusid2-s2.0-85102296226-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusSMALL-INTESTINAL SUBMUCOSA-
dc.subject.keywordPlusMESENCHYMAL STEM-CELLS-
dc.subject.keywordPlusPOROUS SCAFFOLD DESIGN-
dc.subject.keywordPlusEXTRACELLULAR-MATRIX-
dc.subject.keywordPlusDEGRADATION BEHAVIOR-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusBIOMATERIAL-
dc.subject.keywordPlusBONE-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusANGIOGENESIS-
dc.subject.keywordAuthor3d printing-
dc.subject.keywordAuthorPLCL-
dc.subject.keywordAuthordecellularization-
dc.subject.keywordAuthorangiogenesis-
dc.subject.keywordAuthordECM hydrogel-
dc.subject.keywordAuthoradipose tissue regeneration-
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