4.8 Article

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

期刊

CARBON
卷 152, 期 -, 页码 434-443

出版社

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

关键词

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

资金

  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]

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据