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dc.contributor.authorShafiq, Muhammad-
dc.contributor.authorJung, Youngmee-
dc.contributor.authorKim, Soo Hyun-
dc.date.accessioned2024-01-20T04:03:10Z-
dc.date.available2024-01-20T04:03:10Z-
dc.date.created2021-09-04-
dc.date.issued2016-06-
dc.identifier.issn1549-3296-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/124016-
dc.description.abstractThe development of cell-free vascular grafts has tremendous potential for tissue engineering. However, thrombus formation, less-than-ideal cell infiltration, and a lack of growth potential limit the application of electrospun scaffolds for in situ tissue-engineered vasculature. To overcome these challenges, here we present development of an acellular tissue-engineered vessel based on electrospun poly(L-lactide-co--caprolactone) scaffolds. Heparin was conjugated to suppress thrombogenic responses, and substance P (SP) was immobilized to recruit host cells. SP was released in a sustained manner from scaffolds and recruited human bone marrow-derived mesenchymal stem cells. The biocompatibility and biological performance of the grafts were evaluated by in vivo experiments involving subcutaneous scaffold implantation in Sprague-Dawley rats (n=12) for up to 4 weeks. Histological analysis revealed a higher extent of accumulative host cell infiltration, neotissue formation, collagen deposition, and elastin deposition in scaffolds containing either SP or heparin/SP than in the control groups. We also observed the presence of a large number of laminin-positive blood vessels, von Willebrand factor (vWF(+)) cells, and alpha smooth muscle actin-positive cells in the explants containing SP and heparin/SP. Additionally, SP and heparin/SP grafts showed the existence of CD90(+) and CD105(+) MSCs and induced a large number of M2 macrophages to infiltrate the graft wall compared with that observed with the control group. Our cell-free grafts could enhance vascular regeneration by endogenous cell recruitment and by mediating macrophage polarization into the M2 phenotype, suggesting that these constructs may be a promising cell-free graft candidate and are worthy of further in vivo evaluation. (c) 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 1352-1371, 2016.-
dc.languageEnglish-
dc.publisherWILEY-
dc.subjectNEUROPEPTIDE SUBSTANCE-P-
dc.subjectBONE MORPHOGENETIC PROTEIN-2-
dc.subjectPEPTIDE NANOFIBERS-
dc.subjectBLOOD-VESSELS-
dc.subjectRECRUITMENT-
dc.subjectANGIOGENESIS-
dc.subjectSCAFFOLDS-
dc.subjectGROWTH-
dc.subjectPOLY(L-LACTIDE-CO-EPSILON-CAPROLACTONE)-
dc.subjectINFILTRATION-
dc.titleCovalent immobilization of stem cell inducing/recruiting factor and heparin on cell-free small-diameter vascular graft for accelerated in situ tissue regeneration-
dc.typeArticle-
dc.identifier.doi10.1002/jbm.a.35666-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, v.104, no.6, pp.1352 - 1371-
dc.citation.titleJOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A-
dc.citation.volume104-
dc.citation.number6-
dc.citation.startPage1352-
dc.citation.endPage1371-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000375117200004-
dc.identifier.scopusid2-s2.0-84977858260-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusNEUROPEPTIDE SUBSTANCE-P-
dc.subject.keywordPlusBONE MORPHOGENETIC PROTEIN-2-
dc.subject.keywordPlusPEPTIDE NANOFIBERS-
dc.subject.keywordPlusBLOOD-VESSELS-
dc.subject.keywordPlusRECRUITMENT-
dc.subject.keywordPlusANGIOGENESIS-
dc.subject.keywordPlusSCAFFOLDS-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusPOLY(L-LACTIDE-CO-EPSILON-CAPROLACTONE)-
dc.subject.keywordPlusINFILTRATION-
dc.subject.keywordAuthorstem cell-
dc.subject.keywordAuthorvascular graft-
dc.subject.keywordAuthorelectrospinning-
dc.subject.keywordAuthorin situ tissue regeneration-
dc.subject.keywordAuthorneovascularization/angiogenesis-
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