Bright polymer dots tracking stem cell engraftment and migration to injured mouse liver

Dandan Chen, Qiong Li, Zihui Meng, Lei Guo, Ying Tang, Zhihe Liu, Shengyan Yin, Weiping Qin, Zhen Yuan, Xuanjun Zhang, Changfeng Wu

Research output: Contribution to journalArticlepeer-review

51 Scopus citations

Abstract

Stem cell therapy holds promise for treatment of intractable diseases and injured organs. For clinical translation, it is pivotal to understand the homing, engraftment, and differentiation processes of stem cells in a living body. Here we report near-infrared (NIR) fluorescent semiconductor polymer dots (Pdots) for bright labeling and tracking of human mesenchymal stem cells (MSCs). The Pdots exhibit narrow-band emission at 775 nm with a quantum yield of 22%, among the highest value for various NIR probes. The Pdots together with a cell penetrating peptide are able to track stem cells over two weeks without disturbing their multipotent properties, as confirmed by the analyses on cell proliferation, differentiation, stem-cell markers, and immunophenotyping. The in vivo cell tracking was demonstrated in a liver-resection mouse model, which indicated that the Pdot-labeled MSCs after tail-vein transplantation were initially trapped in lung, gradually migrated to the injured liver, and then proliferated into cell clusters. Liver-function analysis and histological examination revealed that the inflammation induced by liver resection was apparently decreased after stem cell transplantation. With the bright labeling, superior biocompatibility, and long-term tracking performance, the Pdot probes are promising for stem cell research and regenerative medicine.

Original languageEnglish
Pages (from-to)1820-1834
Number of pages15
JournalTheranostics
Volume7
Issue number7
DOIs
StatePublished - 2017
Externally publishedYes

Keywords

  • Cell tracking
  • In vivo imaging
  • Near-infrared fluorescence
  • Semiconductor polymer dot
  • Stem cells

Fingerprint

Dive into the research topics of 'Bright polymer dots tracking stem cell engraftment and migration to injured mouse liver'. Together they form a unique fingerprint.

Cite this