Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Shafiq, Muhammad | - |
dc.contributor.author | Jung, Youngmee | - |
dc.contributor.author | Kim, Soo Hyun | - |
dc.date.accessioned | 2024-01-20T04:03:10Z | - |
dc.date.available | 2024-01-20T04:03:10Z | - |
dc.date.created | 2021-09-04 | - |
dc.date.issued | 2016-06 | - |
dc.identifier.issn | 1549-3296 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/124016 | - |
dc.description.abstract | The 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.language | English | - |
dc.publisher | WILEY | - |
dc.subject | NEUROPEPTIDE SUBSTANCE-P | - |
dc.subject | BONE MORPHOGENETIC PROTEIN-2 | - |
dc.subject | PEPTIDE NANOFIBERS | - |
dc.subject | BLOOD-VESSELS | - |
dc.subject | RECRUITMENT | - |
dc.subject | ANGIOGENESIS | - |
dc.subject | SCAFFOLDS | - |
dc.subject | GROWTH | - |
dc.subject | POLY(L-LACTIDE-CO-EPSILON-CAPROLACTONE) | - |
dc.subject | INFILTRATION | - |
dc.title | Covalent immobilization of stem cell inducing/recruiting factor and heparin on cell-free small-diameter vascular graft for accelerated in situ tissue regeneration | - |
dc.type | Article | - |
dc.identifier.doi | 10.1002/jbm.a.35666 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, v.104, no.6, pp.1352 - 1371 | - |
dc.citation.title | JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A | - |
dc.citation.volume | 104 | - |
dc.citation.number | 6 | - |
dc.citation.startPage | 1352 | - |
dc.citation.endPage | 1371 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000375117200004 | - |
dc.identifier.scopusid | 2-s2.0-84977858260 | - |
dc.relation.journalWebOfScienceCategory | Engineering, Biomedical | - |
dc.relation.journalWebOfScienceCategory | Materials Science, Biomaterials | - |
dc.relation.journalResearchArea | Engineering | - |
dc.relation.journalResearchArea | Materials Science | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | NEUROPEPTIDE SUBSTANCE-P | - |
dc.subject.keywordPlus | BONE MORPHOGENETIC PROTEIN-2 | - |
dc.subject.keywordPlus | PEPTIDE NANOFIBERS | - |
dc.subject.keywordPlus | BLOOD-VESSELS | - |
dc.subject.keywordPlus | RECRUITMENT | - |
dc.subject.keywordPlus | ANGIOGENESIS | - |
dc.subject.keywordPlus | SCAFFOLDS | - |
dc.subject.keywordPlus | GROWTH | - |
dc.subject.keywordPlus | POLY(L-LACTIDE-CO-EPSILON-CAPROLACTONE) | - |
dc.subject.keywordPlus | INFILTRATION | - |
dc.subject.keywordAuthor | stem cell | - |
dc.subject.keywordAuthor | vascular graft | - |
dc.subject.keywordAuthor | electrospinning | - |
dc.subject.keywordAuthor | in situ tissue regeneration | - |
dc.subject.keywordAuthor | neovascularization/angiogenesis | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.