| Literature DB >> 33643604 |
Lufei Wang1, Dong Joon Lee1, Han Han2, Lixing Zhao2, Hiroshi Tsukamoto3, Yong-Il Kim4, Adele M Musicant5, Kshitij Parag-Sharma6, Xiangxiang Hu1, Henry C Tseng7, Jen-Tsan Chi8, Zhengyan Wang9, Antonio L Amelio1,10, Ching-Chang Ko11.
Abstract
Bioluminescent imaging (BLI) has emerged as a popular in vivo tracking modality in bone regeneration studies stemming from its clear advantages: non-invasive, real-time, and inexpensive. We recently adopted bioluminescence resonance energy transfer (BRET) principle to improve BLI cell tracking and generated the brightest bioluminescent signal known to date, which thus enables more sensitive real-time cell tracking at deep tissue level. In the present study, we brought BRET-based cell tracking strategy into the field of bone tissue engineering for the first time. We labeled rat mesenchymal stem cells (rMSCs) with our in-house BRET-based GpNLuc reporter and evaluated the cell tracking efficacy both in vitro and in vivo. In scaffold-free spheroid 3D culture system, using BRET-based GpNLuc labeling resulted in significantly better correlation to cell numbers than a fluorescence based approach. In scaffold-based 3D culture system, GpNLuc-rMSCs displayed robust bioluminescence signals with minimal background noise. Furthermore, a tight correlation between BLI signal and cell number highlighted the robust reliability of using BRET-based BLI. In calvarial critical sized defect model, robust signal and the consistency in cell survival evaluation collectively supported BRET-based GpNLuc labeling as a reliable approach for non-invasively tracking MSC. In summary, BRET-based GpNLuc labeling is a robust, reliable, and inexpensive real-time cell tracking method, which offers a promising direction for the technological innovation of BLI and even non-invasive tracking systems, in the field of bone tissue engineering.Entities:
Keywords: Bioluminescent imaging; bioluminescence resonance energy transfer; bone tissue engineering; cell tracking; mesenchymal stem cells
Year: 2021 PMID: 33643604 PMCID: PMC7894599 DOI: 10.1177/2041731421995465
Source DB: PubMed Journal: J Tissue Eng ISSN: 2041-7314 Impact factor: 7.813