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Non-invasive in vivo monitoring of transplanted stem cells in 3D-bioprinted constructs using near-infrared fluorescent imagingoa mark
  • Kim, Soon Hee ;
  • Kwon, Jin Seon ;
  • Cho, Jae Gu ;
  • Park, Kate G. ;
  • Lim, Tae Hyeon ;
  • Kim, Moon Suk ;
  • Choi, Hak Soo ;
  • Park, Chan Hum ;
  • Lee, Sang Jin
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dc.contributor.authorKim, Soon Hee-
dc.contributor.authorKwon, Jin Seon-
dc.contributor.authorCho, Jae Gu-
dc.contributor.authorPark, Kate G.-
dc.contributor.authorLim, Tae Hyeon-
dc.contributor.authorKim, Moon Suk-
dc.contributor.authorChoi, Hak Soo-
dc.contributor.authorPark, Chan Hum-
dc.contributor.authorLee, Sang Jin-
dc.date.issued2021-05-01-
dc.identifier.issn2380-6761-
dc.identifier.urihttps://dspace.ajou.ac.kr/dev/handle/2018.oak/31935-
dc.description.abstractCell-based tissue engineering strategies have been widely established. However, the contributions of the transplanted cells within the tissue-engineered scaffolds to the process of tissue regeneration remain poorly understood. Near-infrared (NIR) fluorescence imaging systems have great potential to non-invasively monitor the transplanted cell-based tissue constructs. In this study, labeling mesenchymal stem cells (MSCs) using a lipophilic pentamethine indocyanine (CTNF127, emission at 700 nm) as a NIR fluorophore was optimized, and the CTNF127-labeled MSCs (NIR-MSCs) were printed embedding in gelatin methacryloyl bioink. The NIR-MSCs-loaded bioink showed excellent printability. In addition, NIR-MSCs in the 3D constructs showed high cell viability and signal stability for an extended period in vitro. Finally, we were able to non-invasively monitor the NIR-MSCs in constructs after implantation in a rat calvarial bone defect model, and the transplanted cells contributed to tissue formation without specific staining. This NIR-based imaging system for non-invasive cell monitoring in vivo could play an active role in validating the cell fate in cell-based tissue engineering applications.-
dc.description.sponsorshipThis study was supported by the following the US National Institutes of Health (NIH) grants: #P41EB023833, #R01EB022230, and #R01HL143020. This work was also supported by the National Research Foundation of South Korea (NRF) grant funded by the Korea government (MSIP; Grant No. NRF-2020R1A2C3010040), Republic of Korea and by the Hallym University Research Fund.-
dc.language.isoeng-
dc.publisherBlackwell Publishing Ltd-
dc.subject.meshMesenchymal stem cell-
dc.subject.meshNear infrared (NIR) fluorescence imaging-
dc.subject.meshNear-infrared fluorescent-
dc.subject.meshTissue constructs-
dc.subject.meshTissue engineering applications-
dc.subject.meshTissue formation-
dc.subject.meshTissue-engineered scaffolds-
dc.subject.meshTransplanted cells-
dc.titleNon-invasive in vivo monitoring of transplanted stem cells in 3D-bioprinted constructs using near-infrared fluorescent imaging-
dc.typeArticle-
dc.citation.titleBioengineering and Translational Medicine-
dc.citation.volume6-
dc.identifier.bibliographicCitationBioengineering and Translational Medicine, Vol.6-
dc.identifier.doi10.1002/btm2.10216-
dc.identifier.scopusid2-s2.0-85103170837-
dc.identifier.urlhttp://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2380-6761-
dc.subject.keywordnear-infrared fluorescence-
dc.subject.keywordnon-invasive monitoring-
dc.subject.keywordscaffold monitoring-
dc.subject.keywordstem cell tracking-
dc.description.isoatrue-
dc.subject.subareaBiotechnology-
dc.subject.subareaBiomedical Engineering-
dc.subject.subareaPharmaceutical Science-
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