4.8 Article

Carbon dots for in vivo fluorescence imaging of adipose tissue-derived mesenchymal stromal cells

Journal

CARBON
Volume 152, Issue -, Pages 434-443

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2019.05.061

Keywords

Carbon dots; Stem cell tracking; Cytotoxicity; In vitro and in vivo optical imaging; Photoluminescence

Funding

  1. Czech-BioImaging large RI project (MEYS CR) [LM2015062]
  2. Ministry of Education, Youth and Sports of the Czech Republic [SVV 260 371/2017, CZ.1.05/2.1.00/19.0377]
  3. Operational Programme Research, Development and Education -European Regional Development Fund of the Ministry of Education, Youth and Sports of the Czech Republic [CZ. 02.1.01/0.0/0.0/16_019/0000754]
  4. project Nano-Envi: Research Infrastructure NanoEnviCz - Ministry of Education, Youth and Sports of the Czech Republic [LM2015073]
  5. Internal Grant Agency of the Charles University in Prague [IGA_PrF_2019_33]
  6. Czech Science Foundation GACR [18-240895]

Ask authors/readers for more resources

Tissue regeneration based on stem cell therapy is one of the most rapidly developing fields of modern medicine. Several properties of human mesenchymal stromal cells (MSCs), such as tropism toward a tumor or injury site, make them promising candidates for regenerative medicine, targeted therapy, or treating injured tissues. However, to fully understand the role of stem cells in therapeutic function, their visualization in vivo is essential. Here, we describe, for the first time, the use of biocompatible quaternized carbon dots (QCDs) as a novel stem-cell tracking probe for in vivo fluorescence imaging of transplanted human MSCs. By studying the in vitro cytotoxicity, intracellular distribution, and precise uptake mechanism, we showed that QCDs had a high biocompatibility and excellent fluorescence properties after 24 h incubation with MSCs. Further to demonstrate the in vivo feasibility of the system, QCD-labeled MSCs (100 mu g/mL of QCDs, 24 h incubation time) were transplanted subcutaneously into an immunodeficient mouse and visualized by optical in vivo imaging. The labeled cells were strongly fluorescent, allowing their semi-quantitative detection. Moreover, the homing of intravenously transplanted QCD-labeled MSCs into the solid tumor was clearly shown. The results demonstrated that QCD-labeling of human MSCs is a highly promising approach for in vivo tracking during stem cell therapy. (C) 2019 Elsevier Ltd. All rights reserved.

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