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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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Publication Year
2021-05-01
Publisher
Blackwell Publishing Ltd
Citation
Bioengineering and Translational Medicine, Vol.6
Keyword
near-infrared fluorescencenon-invasive monitoringscaffold monitoringstem cell tracking
Mesh Keyword
Mesenchymal stem cellNear infrared (NIR) fluorescence imagingNear-infrared fluorescentTissue constructsTissue engineering applicationsTissue formationTissue-engineered scaffoldsTransplanted cells
All Science Classification Codes (ASJC)
BiotechnologyBiomedical EngineeringPharmaceutical Science
Abstract
Cell-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.
ISSN
2380-6761
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/31935
DOI
https://doi.org/10.1002/btm2.10216
Fulltext

Type
Article
Funding
This 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.
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