File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

강현욱

Kang, Hyun-Wook
3D Biofabrication Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.number 3 -
dc.citation.startPage 034101 -
dc.citation.title BIOFABRICATION -
dc.citation.volume 15 -
dc.contributor.author Son, Jeonghyun -
dc.contributor.author Mohamed, Hanan Jamal -
dc.contributor.author Ha, Won -
dc.contributor.author Naren, Aruzhan -
dc.contributor.author Choi, Cham Albert -
dc.contributor.author Kwon, Yoonhee -
dc.contributor.author Park, Sooah -
dc.contributor.author Joung, Hong-Chan -
dc.contributor.author Kang, Hyun-Wook -
dc.date.accessioned 2023-12-21T11:54:46Z -
dc.date.available 2023-12-21T11:54:46Z -
dc.date.created 2023-04-14 -
dc.date.issued 2023-07 -
dc.description.abstract Pre-vascularization has been receiving significant attention for developing implantable engineered 3D tissues. While various pre-vascularization techniques have been developed to improve graft vascularization, the effect of pre-vascularized patterns on in vivo neo-vessel formation has not been studied. In this study, we developed a functional pre-vascularized construct that significantly promotes graft vascularization and conducted in vivo evaluations of the micro-vascular patterns (µVP) in various printed designs. µVP formation, composed of high-density capillaries, was induced by the co-printing of endothelial cells (EC) and adipose-derived stem cells (ADSC). We implanted the printed constructs with various µVP designs into a murine femoral arteriovenous bundle model and evaluated graft vascularization via 3D visualization and immune-histological analysis of the neo-vessels. The µVP-distal group (µVP located away from the host vessel) showed approximately 2-fold improved neo-vascularization compared to the µVP-proximal group (µVP located near the host vessel). Additionally, we confirmed that the µVP-distal group can generate the angiogenic factor gradient spatial environment for graft vascularization via computational simulations. Based on these results, the ADSC mono pattern (AMP), which secretes four times higher angiogenic factors than µVP, was added to the µVP + AMP group design. The µVP + AMP group showed approximately 1.5- and 1.9-fold higher total sprouted neo-vessel volume than the µVP only and AMP only groups, respectively. In immunohistochemical staining analysis, the µVP + AMP group showed 2-fold improved density and diameter of the matured neo-vessels. To summarize, these findings demonstrate graft vascularization accelerated due to design optimization of our pre-vascularized constructs. We believe that the developed pre-vascularization printing technique will facilitate new possibilities for the upscaling of implantable engineered tissues/organs. -
dc.identifier.bibliographicCitation BIOFABRICATION, v.15, no.3, pp.034101 -
dc.identifier.doi 10.1088/1758-5090/acc9de -
dc.identifier.issn 1758-5082 -
dc.identifier.scopusid 2-s2.0-85154557320 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/63998 -
dc.identifier.url http://dx.doi.org/10.1088/1758-5090/acc9de -
dc.identifier.wosid 000976631600001 -
dc.language 영어 -
dc.publisher IOP Publishing Ltd -
dc.title Bioprinting of pre-vascularized constructs for enhanced in vivo neo-vascularization -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Engineering, Biomedical;Materials Science, Biomaterials -
dc.relation.journalResearchArea Engineering;Materials Science -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.